US20130323820A1 - Recombinant microorganisms and uses therefor - Google Patents

Recombinant microorganisms and uses therefor Download PDF

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US20130323820A1
US20130323820A1 US13/909,012 US201313909012A US2013323820A1 US 20130323820 A1 US20130323820 A1 US 20130323820A1 US 201313909012 A US201313909012 A US 201313909012A US 2013323820 A1 US2013323820 A1 US 2013323820A1
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nucleic acid
synthase
bacteria
carboxydotrophic
isolated
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Wendy Yiting Chen
Fungmin Liew
Michael Koepke
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Lanzatech NZ Inc
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Lanzatech New Zealand Ltd
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Priority to US13/909,012 priority Critical patent/US20130323820A1/en
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Assigned to LANZATECH NEW ZEALAND LIMITED reassignment LANZATECH NEW ZEALAND LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHEN, WENDY YITING, KOEPKE, MICHAEL, LIEW, FUNGMIN
Publication of US20130323820A1 publication Critical patent/US20130323820A1/en
Priority to US14/656,827 priority patent/US20150191747A1/en
Priority to US15/867,306 priority patent/US10913958B2/en
Priority to US17/095,064 priority patent/US11459589B2/en
Assigned to LANZATECH NZ, INC. reassignment LANZATECH NZ, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: LANZATECH NEW ZEALAND LIMITED
Assigned to LANZATECH NZ, INC. reassignment LANZATECH NZ, INC. CORRECTIVE ASSIGNMENT TO CORRECT THE U.S. PATENT NUMBER 8,979,228 PREVIOUSLY RECORDED AT REEL: 059911 FRAME: 0400. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Assignors: LANZATECH NEW ZEALAND LIMITED
Assigned to LANZATECH NZ INC. reassignment LANZATECH NZ INC. CORRECTIVE ASSIGNMENT TO CORRECT THE THE PATENT NUMBE 9,5348,20 PREVIOUSLY RECORDED AT REEL: 059911 FRAME: 0400. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Assignors: LANZATECH NEW ZEALAND LIMITED
Priority to US17/823,471 priority patent/US20230013524A1/en
Abandoned legal-status Critical Current

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Definitions

  • the present invention relates to recombinant microorganisms and methods for the production of terpenes and/or precursors thereof by microbial fermentation of a substrate comprising CO.
  • Terpenes are a diverse class of naturally occurring chemicals composed of five-carbon isoprene units.
  • Terpene derivatives include terpenoids (also known as isoprenoids) which may be formed by oxidation or rearrangement of the carbon backbone or a number of functional group additions or rearrangements.
  • terpenes examples include: isoprene (C5 hemiterpene), farnesene (C15 Sesquiterpenes), artemisinin (C15 Sesquiterpenes), citral (C10 Monoterpenes), carotenoids (C40 Tetraterpenes), menthol (C10 Monoterpenes), Camphor (C10 Monoterpenes), and cannabinoids.
  • Terpenes are valuable commercial products used in a diverse number of industries.
  • the highest tonnage uses of terpenes are as resins, solvents, fragrances and vitamins.
  • isoprene is used in the production of synthetic rubber (cis-1,4-polyisoprene) for example in the tyre industry; farnesene is used as an energy dense drop-in fuel used for transportation or as jet-fuel; artemisinin is used as a malaria drug; and citral, carotenoids, menthol, camphor, and cannabinoids are used in the manufacture of pharmaceuticals, butadiene, and as aromatic ingredients.
  • Terpenes may be produced from petrochemical sources and from terpene feed-stocks, such as turpentine.
  • isoprene is produced petrochemically as a by-product of naphtha or oil cracking in the production of ethylene.
  • Many terpenes are also extracted in relatively small quantities from natural sources.
  • these production methods are expensive, unsustainable and often cause environmental problems including contributing to climate change.
  • Microbial fermentation provides an alternative option for the production of terpenes.
  • Terpenes are ubiquitous in nature, for example they are involved in bacterial cell wall biosynthesis, and they are produced by some trees (for example poplar) to protect leaves from UV light exposure.
  • bacteria comprise the necessary cellular machinery to produce terpenes and/or their precursors as metabolic products.
  • carboxydotrophic acetogens such as C. autoethanogenum or C. ljungdahlii , which are able to ferment substrates comprising carbon monoxide to produce products such as ethanol, are not known to produce and emit any terpenes and/or their precursors as metabolic products.
  • most bacteria are not known to produce any terpenes which are of commercial value.
  • the invention generally provides, inter alia, methods for the production of one or more terpenes and/or precursors thereof by microbial fermentation of a substrate comprising CO, and recombinant microorganisms of use in such methods.
  • the invention provides a carboxydotrophic acetogenic recombinant microorganism capable of producing one or more terpenes and/or precursors thereof and optionally one or more other products by fermentation of a substrate comprising CO.
  • the microorganism is adapted to express one or more enzymes in the mevalonate (MVA) pathway not present in a parental microorganism from which the recombinant microorganism is derived (may be referred to herein as an exogenous enzyme).
  • the microorganism is adapted to over-express one or more enzymes in the mevalonate (MVA) pathway which are present in a parental microorganism from which the recombinant microorganism is derived (may be referred to herein as an endogenous enzyme).
  • the microorganism is adapted to:
  • a) express one or more exogenous enzymes in the mevalonate (MVA) pathway and/or overexpress one or more endogenous enzyme in the mevalonate (MVA) pathway; and b) express one or more exogenous enzymes in the DXS pathway and/or overexpress one or more endogenous enzymes in the DXS pathway.
  • the one or more enzymes from the mevalonate (MVA) pathway is selected from the group consisting of:
  • thiolase EC 2.3.1.9
  • HMG-CoA synthase EC 2.3.3.10
  • HMG-CoA reductase EC 1.1.1.88
  • Mevalonate kinase EC 2.7.1.36
  • Phosphomevalonate kinase EC 2.7.4.2
  • f) Mevalonate Diphosphate decarboxylase EC 4.1.1.33
  • the one or more enzymes from the DXS pathway is selected from the group consisting of:
  • one or more further exogenous or endogenous enzymes are expressed or over-expressed to result in the production of a terpene compound or a precursor thereof wherein the exogenous enzyme that is expressed, or the endogenous enzyme that is overexpressed, is selected from the group consisting of:
  • geranyltranstransferase Fps (EC:2.5.1.10), b) heptaprenyl diphosphate synthase (EC:2.5.1.10), c) octaprenyl-diphosphate synthase (EC:2.5.1.90), d) isoprene synthase (EC 4.2.3.27), e) isopentenyl-diphosphate delta-isomerase (EC 5.3.3.2), f) farnesene synthase (EC 4.2.3.46/EC 4.2.3.47), and g) a functionally equivalent variant of any one thereof.
  • the parental microorganism is capable of fermenting a substrate comprising CO to produce Acetyl CoA, but not of converting Acetyl CoA to mevalonic acid or isopentenyl pyrophosphate (IPP) and the recombinant microorganism is adapted to express one or more enzymes involved in the mevalonate pathway.
  • IPP isopentenyl pyrophosphate
  • the one or more terpene and/or precursor thereof is chosen from mevalonic acid, IPP, dimethylallyl pyrophosphate (DMAPP), isoprene, geranyl pyrophosphate (GPP), farnesyl pyrophosphate (FPP) and farnesene.
  • DMAPP dimethylallyl pyrophosphate
  • GPP geranyl pyrophosphate
  • FPP farnesyl pyrophosphate
  • the microorganism comprises one or more exogenous nucleic acids adapted to increase expression of one or more endogenous nucleic acids and which one or more endogenous nucleic acids encode one or more of the enzymes referred to herein before.
  • the one or more exogenous nucleic acids adapted to increase expression is a regulatory element.
  • the regulatory element is a promoter.
  • the promoter is a constitutive promoter. In one embodiment, the promoter is selected from the group comprising Wood-Ljungdahl gene cluster or Phosphotransacetylase/Acetate kinase operon promoters.
  • the microorganism comprises one or more exogenous nucleic acids encoding and adapted to express one or more of the enzymes referred to hereinbefore. In one embodiment, the microorganisms comprise one or more exogenous nucleic acids encoding and adapted to express at least two of the enzymes. In other embodiments, the microorganism comprises one or more exogenous nucleic acids encoding and adapted to express at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine or more of the enzymes.
  • the one or more exogenous nucleic acid is a nucleic acid construct or vector, in one particular embodiment a plasmid, encoding one or more of the enzymes referred to hereinbefore in any combination.
  • the exogenous nucleic acid is an expression plasmid.
  • the parental microorganism is selected from the group of carboxydotrophic acetogenic bacteria.
  • the microorganism is selected from the group comprising Clostridium autoethanogenum, Clostridium ljungdahlii, Clostridium ragsdalei, Clostridium carboxidivorans, Clostridium drakei, Clostridium scatologenes, Clostridium aceticum, Clostridium formicoaceticum, Clostridium magnum, Butyribacterium methylotrophicum, Acetobacterium woodii, Alkalibaculum bacchii, Blautia producta, Eubacterium limosum, Moorella thermoacetica, Moorella thermautotrophica, Sporomusa ovata, Sporomusa silvacetica, Sporomusa sphaeroides, Oxobacter pfennigii , and Thermoanaerobacter kiuvi.
  • the parental microorganism is Clostridium autoethanogenum or Clostridium ljungdahlii .
  • the microorganism is Clostridium autoethanogenum DSM23693.
  • the microorganism is Clostridium ljungdahlii DSM13528 (or ATCC55383).
  • the parental microorganism lacks one or more genes in the DXS pathway and/or the mevalonate (MVA) pathway. In one embodiment, the parental microorganism lacks one or more genes encoding an enzyme selected from the group consisting of:
  • the invention provides a nucleic acid encoding one or more enzymes which when expressed in a microorganism allows the microorganism to produce one or more terpenes and/or precursors thereof by fermentation of a substrate comprising CO.
  • the nucleic acid encodes two or more enzymes which when expressed in a microorganism allows the microorganism to produce one or more terpenes and/or precursors thereof by fermentation of a substrate comprising CO.
  • a nucleic acid of the invention encodes at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine or more of such enzymes.
  • the nucleic acid encodes one or more enzymes in the mevalonate
  • the one or more enzymes is chosen from the group consisting of:
  • a) thiolase (EC 2.3.1.9), b) HMG-CoA synthase (EC 2.3.3.10), c) HMG-CoA reductase (EC 1.1.1.88), d) Mevalonate kinase (EC 2.7.1.36), e) Phosphomevalonate kinase (EC 2.7.4.2), f) Mevalonate Diphosphate decarboxylase (EC 4.1.1.33), and
  • the nucleic acid encodes thiolase (which may be an acetyl CoA c-acetyltransferase), HMG-CoA synthase and HMG-CoA reductase,
  • the nucleic acid encodes one or more enzymes in the mevalonate (MVA) pathway and one or more further nucleic acids in the DXS pathway pathway.
  • the one or more enzymes from the DXS pathway is selected from the group consisting of:
  • the nucleic acid encodes one or more further exogenous or endogenous enzymes are expressed or over-expressed to result in the production of a terpene compound or a precursor thereof wherein the exogenous nucleic acid that is expressed, or the endogenous enzyme that is overexpressed, encodes and enzyme selected from the group consisting of:
  • the nucleic acid encoding thiolase (EC 2.3.1.9) has the sequence SEQ ID NO: 40 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding thiolase (EC 2.3.1.9) is acetyl CoA c-acetyl transferase that has the sequence SEQ ID NO: 41 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding HMG-CoA synthase (EC 2.3.3.10) has the sequence SEQ ID NO: 42 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding HMG-CoA reductase (EC 1.1.1.88) has the sequence SEQ ID NO: 43 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding Mevalonate kinase (EC 2.7.1.36) has the sequence SEQ ID NO: 51 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding Phosphomevalonate kinase (EC 2.7.4.2) has the sequence SEQ ID NO: 52 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding Mevalonate Diphosphate decarboxylase (EC 4.1.1.33) has the sequence SEQ ID NO: 53 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 1-deoxy-D-xylulose-5-phosphate synthase DXS (EC:2.2.1.7) has the sequence SEQ ID NO: 1 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 1-deoxy-D-xylulose 5-phosphate reductoisomerase DXR (EC:1.1.1.267) has the sequence SEQ ID NO: 3 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase IspD (EC:2.7.7.60) has the sequence SEQ ID NO: 5 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase IspE (EC:2.7.1.148) has the sequence SEQ ID NO: 7 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase IspF (EC:4.6.1.12) has the sequence SEQ ID NO: 9 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase IspG (EC:1.17.7.1) has the sequence SEQ ID NO: 11 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 4-hydroxy-3-methylbut-2-enyl diphosphate reductase (EC:1.17.1.2) has the sequence SEQ ID NO: 13 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding geranyltranstransferase Fps has the sequence SEQ ID NO: 15, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding heptaprenyl diphosphate synthase has the sequence SEQ ID NO: 17, or it is a functionally equivalent variant thereof.
  • nucleic acid encoding octaprenyl-diphosphate synthase (EC:2.5.1.90) wherein the octaprenyl-diphosphate synthase is polyprenyl synthetase is encoded by sequence SEQ ID NO: 19, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding isoprene synthase has the sequence SEQ ID NO: 21, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding Isopentenyl-diphosphate delta-isomerase (idi) has the sequence SEQ ID NO: 54, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding farnesene synthase has the sequence SEQ ID NO: 57, or it is a functionally equivalent variant thereof.
  • the nucleic acid encodes the following enzymes:
  • the nucleic acid encodes the following enzymes:
  • HMG-CoA synthase b) HMG-CoA synthase; c) HMG-CoA reductase; d) Mevalonate kinase; e) Phosphomevalonate kinase; f) Mevalonate Diphosphate decarboxylase; g) Isopentenyl-diphosphate delta-isomerase (idi); and h) isoprene synthase; or functionally equivalent variants thereof.
  • the nucleic acid encodes the following enzymes:
  • the nucleic acids of the invention further comprise a promoter.
  • the promoter allows for constitutive expression of the genes under its control.
  • a Wood-Ljungdahl cluster promoter is used.
  • a Phosphotransacetylase/Acetate kinase operon promoter is used.
  • the promoter is from C. autoethanogenum.
  • the invention provides a nucleic acid construct or vector comprising one or more nucleic acid of the second aspect.
  • the nucleic acid construct or vector is an expression construct or vector.
  • the expression construct or vector is a plasmid.
  • the invention provides host organisms comprising any one or more of the nucleic acids of the second aspect or vectors or constructs of the third aspect.
  • the invention provides a composition comprising an expression construct or vector as referred to in the third aspect of the invention and a methylation construct or vector.
  • the composition is able to produce a recombinant microorganism according to the first aspect of the invention.
  • the expression construct/vector and/or the methylation construct/vector is a plasmid.
  • the invention provides a method for the production of one or more terpenes and/or precursors thereof and optionally one or more other products by microbial fermentation comprising fermenting a substrate comprising CO using a recombinant microorganism of the first aspect of the invention.
  • the microorganism is maintained in an aqueous culture medium.
  • the fermentation of the substrate takes place in a bioreactor.
  • the one or more terpene and/or precursor thereof is chosen from mevalonic acid, IPP, dimethylallyl pyrophosphate (DMAPP), isoprene, geranyl pyrophosphate (GPP), farnesyl pyrophosphate (FPP) and farnesene.
  • DMAPP dimethylallyl pyrophosphate
  • GPP geranyl pyrophosphate
  • FPP farnesyl pyrophosphate
  • the substrate comprising CO is a gaseous substrate comprising CO.
  • the substrate comprises an industrial waste gas.
  • the gas is steel mill waste gas or syngas.
  • the substrate will typically contain a major proportion of CO, such as at least about 20% to about 100% CO by volume, from 20% to 70% CO by volume, from 30% to 60% CO by volume, and from 40% to 55% CO by volume.
  • the substrate comprises about 25%, or about 30%, or about 35%, or about 40%, or about 45%, or about 50% CO, or about 55% CO, or about 60% CO by volume.
  • the methods further comprise the step of recovering a terpene and/or precursor thereof and optionally one or more other products from the fermentation broth.
  • the invention provides one or more terpene and/or precursor thereof when produced by the method of the sixth aspect.
  • the one or more terpene and/or precursor thereof is chosen from the group consisting of mevalonic acid, IPP, dimethylallyl pyrophosphate (DMAPP), isoprene, geranyl pyrophosphate (GPP), farnesyl pyrophosphate (FPP) and farnesene.
  • the invention provides a method for the production of a microorganism of the first aspect of the invention comprising transforming a carboxydotrophic acetogenic parental microorganism by introduction of one or more nucleic acids such that the microorganism is capable of producing, or increasing the production of, one or more terpenes and/or precursors thereof and optionally one or more other products by fermentation of a substrate comprising CO, wherein the parental microorganism is not capable of producing, or produces at a lower level, the one or more terpene and/or precursor thereof by fermentation of a substrate comprising CO.
  • a parental microorganism is transformed by introducing one or more exogenous nucleic acids adapted to express one or more enzymes in the mevalonate (MVA) pathway and optionally the DXS pathway.
  • a parental microorganism is transformed with one or more nucleic acids adapted to over-express one or more enzymes in the mevalonate (MVA) pathway and optionally the DXS pathway which are naturally present in the parental microorganism.
  • the one or more enzymes are as herein before described.
  • an isolated, genetically engineered, carboxydotrophic, acetogenic bacteria which comprise an exogenous nucleic acid encoding an enzyme in a mevalonate pathway or in a DXS pathway or in a terpene biosynthesis pathway, whereby the bacteria express the enzyme.
  • the enzyme is selected from the group consisting of:
  • the bacteria do not express the enzyme in the absence of said nucleic acid. In some aspects the bacteria which express the enzyme under anaerobic conditions.
  • the plasmid comprises a nucleic acid encoding an enzyme in a mevalonate pathway or in a DXS pathway or in a terpene biosynthesis pathway, whereby when the plasmid is in the bacteria, the enzyme is expressed by said bacteria.
  • the enzyme is selected from the group consisting of:
  • a process is provided in another embodiment for converting CO and/or CO 2 into isoprene.
  • the process comprises: passing a gaseous CO-containing and/or CO 2 -containing substrate to a bioreactor containing a culture of carboxydotrophic, acetogenic bacteria in a culture medium such that the bacteria convert the CO and/or CO 2 to isoprene, and recovering the isoprene from the bioreactor.
  • the carboxydotrophic acetogenic bacteria are genetically engineered to express a isoprene synthase.
  • Another embodiment provides an isolated, genetically engineered, carboxydotrophic, acetogenic bacteria which comprise a nucleic acid encoding an isoprene synthase.
  • the bacteria express the isoprene synthase and the bacteria are able to convert imethylallyldiphosphate to isoprene.
  • the isoprene synthase is a Populus tremuloides enzyme.
  • the nucleic acid is codon optimized.
  • expression of the isoprene synthase is under the transcriptional control of a promoter for a pyruvate: ferredoxin oxidoreductase gene from Clostridium autoethanogenum.
  • Another embodiment provides a process for converting CO and/or CO 2 into isopentyldiphosphate (IPP).
  • the process comprises: passing a gaseous CO-containing and/or CO 2 -containing substrate to a bioreactor containing a culture of carboxydotrophic, acetogenic bacteria in a culture medium such that the bacteria convert the CO and/or CO 2 to isopentyldiphosphate (IPP), and recovering the IPP from the bioreactor.
  • the carboxydotrophic acetogenic bacteria are genetically engineered to express a isopentyldiphosphate delta isomerase.
  • Still another embodiment provides isolated, genetically engineered, carboxydotrophic, acetogenic bacteria which comprise a nucleic acid encoding an isopentyldiphosphate delta isomerase.
  • the bacteria express the isopentyldiphosphate delta isomerase and the bacteria are able to convert dimethylallyldiphosphate to isopentyldiphosphate.
  • the nucleic acid encodes a Clostridium beijerinckii isopentyldiphosphate delta isomerase.
  • the nucleic acid is under the transcriptional control of a promoter for a pyruvate: ferredoxin oxidoreductase gene from Clostridium autoethanogenum .
  • the nucleic acid is under the transcriptional control of a promoter for a pyruvate: ferredoxin oxidoreductase gene from Clostridium autoethanogenum and downstream of a second nucleic acid encoding an isoprene synthase.
  • Still another embodiment provides a process for converting CO and/or CO 2 into isopentyldiphosphate (IPP) and/or isoprene.
  • the process comprises: passing a gaseous CO-containing and/or CO 2 -containing substrate to a bioreactor containing a culture of carboxydotrophic, acetogenic bacteria in a culture medium such that the bacteria convert the CO and/or CO 2 to isopentyldiphosphate (IPP) and/or isoprene, and recovering the IPP and/or isoprene from the bioreactor.
  • the carboxydotrophic acetogenic bacteria are genetically engineered to have an increased copy number of a nucleic acid encoding a deoxyxylulose 5-phosphate synthase (DXS) enzyme, wherein the increased copy number is greater than 1 per genome.
  • DXS deoxyxylulose 5-phosphate synthase
  • Yet another embodiment provides isolated, genetically engineered, carboxydotrophic, acetogenic bacteria which comprise a copy number of greater than 1 per genome of a nucleic acid encoding a deoxyxylulose 5-phosphate synthase (DXS) enzyme.
  • the isolated, genetically engineered, carboxydotrophic, acetogenic bacteria may further comprise a nucleic acid encoding an isoprene synthase.
  • the isolated, genetically engineered, carboxydotrophic, acetogenic bacteria of may further comprise a nucleic acid encoding an isopentyldiphosphate delta isomerase.
  • the isolated, genetically engineered, carboxydotrophic, acetogenic bacteria may further comprise a nucleic acid encoding an isopentyldiphosphate delta isomerase and a nucleic acid encoding an isoprene synthase.
  • Another embodiment provides isolated, genetically engineered, carboxydotrophic, acetogenic bacteria which comprise a nucleic acid encoding a phosphomevalonate kinase (PMK).
  • the bacteria express the encoded enzyme and the enzyme is not native to the bacteria.
  • the enzymes are Staphylococcus aureus enzymes.
  • the enzyme is expressed under the control of one or more C. autoethanogenum promoters.
  • the bacteria further comprise a nucleic acid encoding thiolase (thlA/vraB), a nucleic acid encoding a HMG-CoA synthase (HMGS), and a nucleic acid encoding an HMG-CoA reductase (HMGR).
  • thiolase is Clostridium acetobutylicum thiolase.
  • the bacteria further comprise a nucleic acid encoding a mevalonate disphosphate decarboxylase (PMD).
  • Still another embodiment provides isolated, genetically engineered, carboxydotrophic, acetogenic bacteria which comprise an exogenous nucleic acid encoding alpha-farnesene synthase.
  • the nucleic acid is codon optimized for expression in C. autoethanogenum .
  • the alpha-farnesene synthase is a Malus ⁇ domestica alpha-farnesene synthase.
  • the bacteria further comprise a nucleic acid segment encoding geranyltranstransferase.
  • the germayltranstransferase is an E. coli geranyltranstransferase.
  • Suitable isolated, genetically engineered, carboxydotrophic, acetogenic bacteria for any of the aspects or embodiments of the invention may be selected from the group consisting of Clostridium autoethanogenum, Clostridium ljungdahlii, Clostridium ragsdalei, Clostridium carboxidivorans, Clostridium drakei, Clostridium scatologenes, Clostridium aceticum, Clostridium formicoaceticum, Clostridium magnum, Butyribacterium methylotrophicum, Acetobacterium woodii, Alkalibaculum bacchii, Blautia producta, Eubacterium limosum, Moorella thermoacetica, Moorella thermautotrophica, Sporomusa ovata, Sporomusa silvacetica, Sporomusa sphaeroides, Oxobacter pfennigii , and Thermoanaerobacter kiuvi.
  • the invention may also be said broadly to consist in the parts, elements and features referred to or indicated in the specification of the application, individually or collectively, in any or all combinations of two or more of said parts, elements or features, and where specific integers are mentioned herein which have known equivalents in the art to which the invention relates, such known equivalents are deemed to be incorporated herein as if individually set forth.
  • FIG. 1 Pathway diagram for production of terpenes, gene targets described in this application are highlighted with bold arrows.
  • FIG. 2 Genetic map of plasmid pMTL 85146-ispS
  • FIG. 3 Genetic map of plasmid pMTL 85246-ispS-idi
  • FIG. 4 Genetic map of plasmid pMTL 85246-ispS-idi-dxs
  • FIG. 5 Sequencing results for plasmid pMTL 85246-ispS-idi-dxs
  • FIG. 6 Comparison of energetics for production of terpenes from CO via DXS and mevalonate pathway
  • FIG. 7 Mevalonate pathway
  • FIG. 8 Agarose gel electrophoresis image confirming presence of isoprene expression plasmid pMTL 85246-ispS-idi in C. autoethanogenum transformants.
  • Lanes 1, and 20 show 100 bp Plus DNA Ladder.
  • Lane 3-6, 9-12, 15-18 show PCR with isolated plasmids from 4 different clones as template, each in the following order: colE1, ermB, and idi.
  • Lanes 2, 8, and 14 show PCR without template as negative control, each in the following order: colE1, ermB, and idi.
  • Lanes 7, 13, and 19 show PCR with pMTL 85246-ispS-idi from E. coli as positive control, each in the following order: colE1, ermB, and idi.
  • FIG. 9 Mevalonate expression plasmid pMTL8215-Pptaack-thlA-HMGS-Patp-HMGR
  • FIG. 10 Isoprene expression plasmid pMTL 8314-Pptaack-thlA-HMGS-Patp-HMGR-Pmf-MK-PMK-PMD-Pfor-idi-ispS
  • FIG. 11 Farnesene expression plasmid pMTL8314-Pptaack-thlA-HMGS-Patp-HMGR-Prnf-MK-PMK-PMD-Pfor-idi-ispA-FS
  • FIG. 12 Genetic map of plasmid pMTL 85246-ispS-idi-dxs
  • FIG. 13 Amplification chart for gene expression experiment with C. autoethanogenum carrying plasmid pMTL 85146-ispS
  • FIG. 14 Amplification chart for gene expression experiment with C. autoethanogenum carrying plasmid pMTL 85246-ispS-idi
  • FIG. 15 Amplification chart for gene expression experiment with C. autoethanogenum carrying plasmid pMTL 85246-ispS-idi-dxs
  • FIG. 16 PCR check for the presence of the plasmid pMTL8314Prnf-MK-PMK-PMD-Pfor-idi-ispA-FS. Expected band size 1584 bp. The DNA marker Fermentas 1 kb DNA ladder.
  • FIG. 17 Growth curve for transformed C. autoethanogemun carrying plasmid pMTL8314Prnf-MK-PMK-PMD-Pfor-idi-ispA-FS
  • FIG. 18 RT-PRC data showing the expression of the genes Mevalonate kinase (MK SEQ ID NO: 51), Phosphomevalonate Kinase (PMK SEQ ID NO: 52), Mevalonate Diphosphate Decarboxylase (PMD SEQ ID NO: 53), Isopentyl-diphosphate Delta-isomerase (idi SEQ ID NO: 54), Geranyltranstransferase (ispA SEQ ID NO: 56) and Farnesene synthase (FS SEQ ID NO: 57).
  • MK SEQ ID NO: 51 Mevalonate kinase
  • PMK SEQ ID NO: 52 Phosphomevalonate Kinase
  • PMD SEQ ID NO: 53 Mevalonate Diphosphate Decarboxylase
  • idi SEQ ID NO: 54 Isopentyl-diphosphate Delta-isomerase
  • Geranyltranstransferase ispA SEQ ID NO: 56
  • FIG. 19 GC-MS detection and conformation of the presence of farnesene in 1 mM mevalonate spiked cultures carrying pMTL8314Prnf-MK-PMK-PMD-Pfor-idi-ispA-FS.
  • GC-MS chromatogram scanned for peaks containing ions with a mass of 93. Chromatogram 1 and 2 are transformed C. autoethanogenum, 3 is beta-farnesene standard run at the same time as the C. autoethanogenum samples. 4 is E.
  • beta-farnesene standard run at the time of the E. coli samples.
  • the difference in retention time between the E. coli and the C. autoethanogenum samples are due to minor changes to the instrument.
  • the difference in retention time between the beta-farnesene standard and the produced alpha-farnesene are the exact same in both cases, which together with the match in mass spectra's confirm the production of alpha-farnesene in C. autoethanogenum.
  • FIG. 20 MS spectrums for peaks labeled 1A and 2A in FIG. 19 .
  • the MS spectra's matches up with the NIST database spectra ( FIG. 21 ) confirming the peak is alpha-farnesene.
  • FIG. 21 MS spectrum for alpha-farnesen from the NIST Mass Spectral Database.
  • the inventors have surprisingly been able to engineer a carboxydotrophic acetogenic microorganism to produce terpene and precursors thereof including isoprene and farnesene by fermentation of a substrate comprising CO.
  • This offers an alternative means for the production of these products which may have benefits over the current methods for their production.
  • it offers a means of using carbon monoxide from industrial processes which would otherwise be released into the atmosphere and pollute the environment.
  • a “fermentation broth” is a culture medium comprising at least a nutrient media and bacterial cells.
  • a “shuttle microorganism” is a microorganism in which a methyltransferase enzyme is expressed and is distinct from the destination microorganism.
  • a “destination microorganism” is a microorganism in which the genes included on an expression construct/vector are expressed and is distinct from the shuttle microorganism.
  • main fermentation product is intended to mean the one fermentation product which is produced in the highest concentration and/or yield.
  • increasing the efficiency when used in relation to a fermentation process, include, but are not limited to, increasing one or more of the rate of growth of microorganisms catalysing the fermentation, the growth and/or product production rate at elevated product concentrations, the volume of desired product produced per volume of substrate consumed, the rate of production or level of production of the desired product, and the relative proportion of the desired product produced compared with other by-products of the fermentation.
  • substrate comprising carbon monoxide and like terms should be understood to include any substrate in which carbon monoxide is available to one or more strains of bacteria for growth and/or fermentation, for example.
  • gaseous substrate comprising carbon monoxide includes any gas which contains a level of carbon monoxide.
  • the substrate contains at least about 20% to about 100% CO by volume, from 20% to 70% CO by volume, from 30% to 60% CO by volume, and from 40% to 55% CO by volume.
  • the substrate comprises about 25%, or about 30%, or about 35%, or about 40%, or about 45%, or about 50% CO, or about 55% CO, or about 60% CO by volume.
  • the substrate may comprise an approx 2:1, or 1:1, or 1:2 ratio of H 2 :CO.
  • the substrate comprises about 30% or less H 2 by volume, 20% or less H 2 by volume, about 15% or less H 2 by volume or about 10% or less H 2 by volume.
  • the substrate stream comprises low concentrations of H 2 , for example, less than 5%, or less than 4%, or less than 3%, or less than 2%, or less than 1%, or is substantially hydrogen free.
  • the substrate may also contain some CO 2 for example, such as about 1% to about 80% CO 2 by volume, or 1% to about 30% CO 2 by volume. In one embodiment the substrate comprises less than or equal to about 20% CO 2 by volume. In particular embodiments the substrate comprises less than or equal to about 15% CO 2 by volume, less than or equal to about 10% CO 2 by volume, less than or equal to about 5% CO 2 by volume or substantially no CO 2 .
  • the gaseous substrate may be provided in alternative forms.
  • the gaseous substrate containing CO may be provided dissolved in a liquid.
  • a liquid is saturated with a carbon monoxide containing gas and then that liquid is added to the bioreactor. This may be achieved using standard methodology.
  • a microbubble dispersion generator Hensirisak et. al. Scale-up of microbubble dispersion generator for aerobic fermentation; Applied Biochemistry and Biotechnology Volume 101, Number 3/October, 2002
  • the gaseous substrate containing CO may be adsorbed onto a solid support.
  • Such alternative methods are encompassed by use of the term “substrate containing CO” and the like.
  • the CO-containing gaseous substrate is an industrial off or waste gas.
  • “Industrial waste or off gases” should be taken broadly to include any gases comprising CO produced by an industrial process and include gases produced as a result of ferrous metal products manufacturing, non-ferrous products manufacturing, petroleum refining processes, gasification of coal, gasification of biomass, electric power production, carbon black production, and coke manufacturing. Further examples may be provided elsewhere herein.
  • the phrases “fermenting”, “fermentation process” or “fermentation reaction” and the like, as used herein, are intended to encompass both the growth phase and product biosynthesis phase of the process.
  • the bioreactor may comprise a first growth reactor and a second fermentation reactor.
  • the addition of metals or compositions to a fermentation reaction should be understood to include addition to either or both of these reactors.
  • bioreactor includes a fermentation device consisting of one or more vessels and/or towers or piping arrangement, which includes the Continuous Stirred Tank Reactor (CSTR), Immobilized Cell Reactor (ICR), Trickle Bed Reactor (TBR), Bubble Column, Gas Lift Fermenter, Static Mixer, or other vessel or other device suitable for gas-liquid contact.
  • CSTR Continuous Stirred Tank Reactor
  • ICR Immobilized Cell Reactor
  • TBR Trickle Bed Reactor
  • Bubble Column Gas Lift Fermenter
  • Static Mixer Static Mixer
  • Exogenous nucleic acids are nucleic acids which originate outside of the microorganism to which they are introduced. Exogenous nucleic acids may be derived from any appropriate source, including, but not limited to, the microorganism to which they are to be introduced (for example in a parental microorganism from which the recombinant microorganism is derived), strains or species of microorganisms which differ from the organism to which they are to be introduced, or they may be artificially or recombinantly created.
  • the exogenous nucleic acids represent nucleic acid sequences naturally present within the microorganism to which they are to be introduced, and they are introduced to increase expression of or over-express a particular gene (for example, by increasing the copy number of the sequence (for example a gene), or introducing a strong or constitutive promoter to increase expression).
  • the exogenous nucleic acids represent nucleic acid sequences not naturally present within the microorganism to which they are to be introduced and allow for the expression of a product not naturally present within the microorganism or increased expression of a gene native to the microorganism (for example in the case of introduction of a regulatory element such as a promoter).
  • the exogenous nucleic acid may be adapted to integrate into the genome of the microorganism to which it is to be introduced or to remain in an extra-chromosomal state.
  • Exogenous may also be used to refer to proteins. This refers to a protein that is not present in the parental microorganism from which the recombinant microorganism is derived.
  • endogenous as used herein in relation to a recombinant microorganism and a nucleic acid or protein refers to any nucleic acid or protein that is present in a parental microorganism from which the recombinant microorganism is derived.
  • nucleic acids whose sequence varies from the sequences specifically exemplified herein provided they perform substantially the same function.
  • nucleic acid sequences that encode a protein or peptide this means that the encoded protein or peptide has substantially the same function.
  • nucleic acid sequences that represent promoter sequences the variant sequence will have the ability to promote expression of one or more genes.
  • Such nucleic acids may be referred to herein as “functionally equivalent variants”.
  • functionally equivalent variants of a nucleic acid include allelic variants, fragments of a gene, genes which include mutations (deletion, insertion, nucleotide substitutions and the like) and/or polymorphisms and the like.
  • Homologous genes from other microorganisms may also be considered as examples of functionally equivalent variants of the sequences specifically exemplified herein. These include homologous genes in species such as Clostridium acetobutylicum, Clostridium beijerinckii, C. saccharobutylicum and C. saccharoperbutylacetonicum , details of which are publicly available on websites such as Genbank or NCBI.
  • the phrase “functionally equivalent variants” should also be taken to include nucleic acids whose sequence varies as a result of codon optimisation for a particular organism.
  • “Functionally equivalent variants” of a nucleic acid herein will preferably have at least approximately 70%, preferably approximately 80%, more preferably approximately 85%, preferably approximately 90%, preferably approximately 95% or greater nucleic acid sequence identity with the nucleic acid identified.
  • a functionally equivalent variant of a protein or a peptide includes those proteins or peptides that share at least 40%, preferably 50%, preferably 60%, preferably 70%, preferably 75%, preferably 80%, preferably 85%, preferably 90%, preferably 95% or greater amino acid identity with the protein or peptide identified and has substantially the same function as the peptide or protein of interest.
  • variants include within their scope fragments of a protein or peptide wherein the fragment comprises a truncated form of the polypeptide wherein deletions may be from 1 to 5, to 10, to 15, to 20, to 25 amino acids, and may extend from residue 1 through 25 at either terminus of the polypeptide, and wherein deletions may be of any length within the region; or may be at an internal location.
  • Functionally equivalent variants of the specific polypeptides herein should also be taken to include polypeptides expressed by homologous genes in other species of bacteria, for example as exemplified in the previous paragraph.
  • “Substantially the same function” as used herein is intended to mean that the nucleic acid or polypeptide is able to perform the function of the nucleic acid or polypeptide of which it is a variant.
  • a variant of an enzyme of the invention will be able to catalyse the same reaction as that enzyme.
  • the variant has the same level of activity as the polypeptide or nucleic acid of which it is a variant.
  • a functionally equivalent variant has substantially the same function as the nucleic acid or polypeptide of which it is a variant using any number of known methods.
  • “Over-express”, “over expression” and like terms and phrases when used in relation to the invention should be taken broadly to include any increase in expression of one or more proteins (including expression of one or more nucleic acids encoding same) as compared to the expression level of the protein (including nucleic acids) of a parental microorganism under the same conditions. It should not be taken to mean that the protein (or nucleic acid) is expressed at any particular level.
  • a “parental microorganism” is a microorganism used to generate a recombinant microorganism of the invention.
  • the parental microorganism may be one that occurs in nature (ie a wild type microorganism) or one that has been previously modified but which does not express or over-express one or more of the enzymes that are the subject of the present invention. Accordingly, the recombinant microorganisms of the invention may have been modified to express or over-express one or more enzymes that were not expressed or over-expressed in the parental microorganism.
  • nucleic acid “constructs” or “vectors” and like terms should be taken broadly to include any nucleic acid (including DNA and RNA) suitable for use as a vehicle to transfer genetic material into a cell.
  • the terms should be taken to include plasmids, viruses (including bacteriophage), cosmids and artificial chromosomes.
  • Constructs or vectors may include one or more regulatory elements, an origin of replication, a multicloning site and/or a selectable marker.
  • the constructs or vectors are adapted to allow expression of one or more genes encoded by the construct or vector.
  • Nucleic acid constructs or vectors include naked nucleic acids as well as nucleic acids formulated with one or more agents to facilitate delivery to a cell (for example, liposome-conjugated nucleic acid, an organism in which the nucleic acid is contained).
  • a “terpene” as referred to herein should be taken broadly to include any compound made up of C 5 isoprene units joined together including simple and complex terpenes and oxygen-containing terpene compounds such as alcohols, aldehydes and ketones.
  • Simple terpenes are found in the essential oils and resins of plants such as conifers.
  • More complex terpenes include the terpenoids and vitamin A, carotenoid pigments (such as lycopene), squalene, and rubber.
  • monoterpenes include, but are not limited to isoprene, pinene, nerol, citral, camphor, menthol, limonene.
  • sesquiterpenes include but are not limited to nerolidol, farnesol.
  • diterpenes include but are not limited to phytol, vitamin A 1 .
  • Squalene is an example of a triterpene, and carotene (provitamin A 1 ) is a tetraterpene.
  • a “terpene precursor” is a compound or intermediate produced during the reaction to form a terpene starting from Acetyl CoA and optionally pyruvate.
  • the term refers to a precursor compound or intermediate found in the mevalonate (MVA) pathway and optionally the DXS pathway as well as downstream precursors of longer chain terpenes, such as FPP and GPP.
  • MVA mevalonate
  • DXS dimethylallyl pyrophosphate
  • FPP farnesyl pyrophosphate
  • the “DXS pathway” is the enzymatic pathway from pyruvate and D-glyceraldehyde-3-phosphate to DMAPP or IPP. It is also known as the deoxyxylulose 5-phosphate (DXP/DXPS/DOXP or DXS)/methylerythritol phosphate (MEP) pathway.
  • DXP/DXPS/DOXP or DXS deoxyxylulose 5-phosphate
  • MEP methylerythritol phosphate
  • the “mevalonate (MVA) pathway” is the enzymatic pathway from acetyl-CoA to IPP.
  • DXP/DXPS/DOXP or DXS deoxyxylulose 5-phosphate
  • MEP methylerythritol phosphate
  • G3P D-glyceraldehyde-3-phosphate
  • MAA mevalonate
  • Genomes of carboxydotrophic acetogens C. autoethanogenum, C. ljungdahlii were analysed by the inventors for presence of either of the two pathways. All genes of the DXS pathway were identified in C. autoethanogenum and C. ljungdahlii (Table 1), while the mevalonate pathway is absent. Additionally, carboxydotrophic acetogens such as C. autoethanogenum or C. ljungdahlii are not known to produce any terpenes as metabolic end products.
  • Terpenes are energy dense compounds, and their synthesis requires the cell to invest energy in the form of nucleoside triposphates such as ATP.
  • Using sugar as a substrate requires sufficient energy to be supplied from glycolysis to yield several molecules of ATP.
  • the production of terpenes and/or their precursors via the DXS pathway using sugar as a substrate proceeds in a relatively straightforward manner due to the availability of pyruvate and D-glyceraldehyde-3-phosphate (G3P), G3P being derived from C5 pentose and C6 hexose sugars. These C5 and C6 molecules are thus relatively easily converted into C5 isoprene units from which terpenes are composed.
  • the mevalonate pathway requires less nucleoside triposphates as ATP, less reducing equivalents, and is also more direct when compared to the DXS pathway with only six necessary reaction steps from acetyl-CoA. This provides advantages in the speed of the reactions and metabolic fluxes and increases overall energy efficiency. Additionally, the lower number of enzymes required simplifies the recombination method required to produce a recombinant microorganism.
  • Anaerobic production of isoprene has the advantage of providing a safer operating environment because isoprene is extremely flammable in the presence of oxygen and has a lower flammable limit (LFL) of 1.5-2.0% and an upper flammable (UFL) limit of 2.0-12% at room temperature and atmospheric pressure.
  • LFL lower flammable limit
  • UNL upper flammable limit
  • the invention provides a recombinant microorganism capable of producing one or more terpenes and/or precursors thereof, and optionally one or more other products, by fermentation of a substrate comprising CO.
  • the microorganism is adapted to: express one or more exogenous enzymes from the mevalonate (MVA) pathway and/or overexpress one or more endogenous enzyme from the mevalonate (MVA) pathway; and
  • a) express one or more exogenous enzymes from the DXS pathway and/or overexpress one or more endogenous enzymes from the DXS pathway.
  • the parental microorganism from which the recombinant microorganism is derived is capable of fermenting a substrate comprising CO to produce Acetyl CoA, but not of converting Acetyl CoA to mevalonic acid or isopentenyl pyrophosphate (IPP) and the recombinant microorganism is adapted to express one or more enzymes involved in the mevalonate pathway.
  • IPP isopentenyl pyrophosphate
  • the microorganism may be adapted to express or over-express the one or more enzymes by any number of recombinant methods including, for example, increasing expression of native genes within the microorganism (for example, by introducing a stronger or constitutive promoter to drive expression of a gene), increasing the copy number of a gene encoding a particular enzyme by introducing exogenous nucleic acids encoding and adapted to express the enzyme, introducing an exogenous nucleic acid encoding and adapted to express an enzyme not naturally present within the parental microorganism.
  • the one or more enzymes are from the mevalonate (MVA) pathway and are selected from the group consisting of:
  • thiolase EC 2.3.1.9
  • HMG-CoA synthase EC 2.3.3.10
  • HMG-CoA reductase EC 1.1.1.88
  • Mevalonate kinase EC 2.7.1.36
  • Phosphomevalonate kinase EC 2.7.4.2
  • f) Mevalonate Diphosphate decarboxylase EC 4.1.1.33
  • the optional one or more enzymes are from the DXS pathway is selected from the group consisting of:
  • one or more exogenous or endogenous further enzymes are expressed or over-expressed to result in the production of a terpene compound and/or precursor thereof wherein the exogenous enzyme that is expressed, or the endogenous enzyme that is overexpressed is selected from the group consisting of:
  • geranyltranstransferase Fps (EC:2.5.1.10), b) heptaprenyl diphosphate synthase (EC:2.5.1.10), c) octaprenyl-diphosphate synthase (EC:2.5.1.90), d) isoprene synthase (EC 4.2.3.27), e) isopentenyl-diphosphate delta-isomerase (EC EC 5.3.3.2), f) farnesene synthase (EC 4.2.3.46/EC 4.2.3.47), and g) a functionally equivalent variant of any one thereof.
  • sequence information for each of the enzymes is listed in the figures herein.
  • the enzymes of use in the microorganisms of the invention may be derived from any appropriate source, including different genera and species of bacteria, or other organisms. However, in one embodiment, the enzymes are derived from Staphylococcus aureus.
  • the enzyme isoprene synthase is derived from Poplar tremuloides .
  • it has the nucleic acid sequence exemplified in SEQ ID NO: 21 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme deoxyxylulose 5-phosphate synthase is derived from C. autoethanogenum , encoded by the nucleic acid sequence exemplified in SEQ ID NO: 1 and/or with the amino acid sequence exemplified in SEQ ID NO: 2 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme 1-deoxy-D-xylulose 5-phosphate reductoisomerase DXR is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 3 or is a functionally equivalent variant thereof.
  • the enzyme 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase IspD is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 5 or is a functionally equivalent variant thereof.
  • the enzyme 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase IspE is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 7 or is a functionally equivalent variant thereof.
  • the enzyme 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase IspF is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 9 or is a functionally equivalent variant thereof.
  • the enzyme 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase IspG is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 11 or is a functionally equivalent variant thereof.
  • the enzyme 4-hydroxy-3-methylbut-2-enyl diphosphate reductase is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 13 or is a functionally equivalent variant thereof.
  • the enzyme mevalonate kinase is derived from Staphylococcus aureus subsp. aureus Mu50 and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 51 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme phosphomevalonate kinase is derived from Staphylococcus aureus subsp. aureus Mu50 and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 52 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme mevalonate diphosphate decarboxylase is derived from Staphylococcus aureus subsp. aureus Mu50 and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 53 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme Isopentenyl-diphosphate delta-isomerase (idi) is derived from Clostridium beijerinckii and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 54 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme thiolase is derived from Clostridium acetobutylicum ATCC824 and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 40 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme is a thiolase enzyme, and is an acetyl-CoA c-acetyltransferase (vraB) derived from Staphylococcus aureus subsp. aureus Mu50 and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 41 hereinafter, or it is a functionally equivalent variant thereof.
  • vraB acetyl-CoA c-acetyltransferase
  • the enzyme 3-hydroxy-3-methylglutaryl-CoA synthase is derived from Staphylococcus aureus subsp. aureus Mu50 and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 42 hereinafter, or it is a functionally equivalent variant thereof.
  • HMGR Hydroxymethylglutaryl-CoA reductase
  • Staphylococcus aureus subsp. aureus Mu50 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 43 hereinafter, or it is a functionally equivalent variant thereof.
  • Geranyltranstransferase is derived from Escherichia coli str. K-12 substr. MG1655 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 56 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzyme heptaprenyl diphosphate synthase is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 17 or is a functionally equivalent variant thereof.
  • the enzyme polyprenyl synthetase is derived from C. autoethanogenum and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 19 or is a functionally equivalent variant thereof.
  • Alpha-farnesene synthase is derived from Malus ⁇ domestica and is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 57 hereinafter, or it is a functionally equivalent variant thereof.
  • the enzymes and functional variants of use in the microorganisms may be identified by assays known to one of skill in the art.
  • the enzyme isoprene synthase may be identified by the method outlined Silver et al. (1991 , Plant Physiol. 97: 1588-1591) or Zhao et al. (2011 , Appl Microbiol Biotechnol, 90:1915-1922).
  • the enzyme farnesene synthase may be identified by the method outlined in Green et al., 2007, Phytochemistry; 68:176-188.
  • enzymes from the mevalonate pathway may be identified by the method outlined in Cabano et al.
  • the 1-deoxy-D-xylulose 5-phosphate synthase of the DXS pathway can be assayed using the method outlined in Kuzuyama et al. (2000 , J. Bacteriol. 182, 891-897). It is also possible to identify genes of DXS and mevalonate pathway using inhibitors like fosmidomycin or mevinoline as described by Trutko et al. (2005 , Microbiology 74: 153-158).
  • the microorganism comprises one or more exogenous nucleic acids adapted to increase expression of one or more endogenous nucleic acids and which one or more endogenous nucleic acids encode one or more of the enzymes referred to herein before.
  • the one or more exogenous nucleic acid adapted to increase expression is a regulatory element.
  • the regulatory element is a promoter.
  • the promoter is a constitutive promoter that is preferably highly active under appropriate fermentation conditions. Inducible promoters could also be used.
  • the promoter is selected from the group comprising Wood-Ljungdahl gene cluster or Phosphotransacetylase/Acetate kinase operon promoters. It will be appreciated by those of skill in the art that other promoters which can direct expression, preferably a high level of expression under appropriate fermentation conditions, would be effective as alternatives to the exemplified embodiments.
  • the microorganism comprises one or more exogenous nucleic acids encoding and adapted to express one or more of the enzymes referred to herein before.
  • the microorganisms comprise one or more exogenous nucleic acid encoding and adapted to express at least two, at least of the enzymes.
  • the microorganism comprises one or more exogenous nucleic acid encoding and adapted to express at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine or more of the enzymes.
  • the microorganism comprises one or more exogenous nucleic acid encoding an enzyme of the invention or a functionally equivalent variant thereof.
  • the microorganism may comprise one or more exogenous nucleic acids. Where it is desirable to transform the parental microorganism with two or more genetic elements (such as genes or regulatory elements (for example a promoter)) they may be contained on one or more exogenous nucleic acids.
  • two or more genetic elements such as genes or regulatory elements (for example a promoter)
  • the one or more exogenous nucleic acid is a nucleic acid construct or vector, in one particular embodiment a plasmid, encoding one or more of the enzymes referred to hereinbefore in any combination.
  • the exogenous nucleic acids may remain extra-chromosomal upon transformation of the parental microorganism or may intergrate into the genome of the parental microorganism. Accordingly, they may include additional nucleotide sequences adapted to assist integration (for example, a region which allows for homologous recombination and targeted integration into the host genome) or expression and replication of an extrachromosomal construct (for example, origin of replication, promoter and other regulatory elements or sequences).
  • the exogenous nucleic acids encoding one or enzymes as mentioned herein before will further comprise a promoter adapted to promote expression of the one or more enzymes encoded by the exogenous nucleic acids.
  • the promoter is a constitutive promoter that is preferably highly active under appropriate fermentation conditions. Inducible promoters could also be used.
  • the promoter is selected from the group comprising Wood-Ljungdahl gene cluster and Phosphotransacetylase/Acetate kinase promoters. It will be appreciated by those of skill in the art that other promoters which can direct expression, preferably a high level of expression under appropriate fermentation conditions, would be effective as alternatives to the exemplified embodiments.
  • the exogenous nucleic acid is an expression plasmid.
  • the parental microorganism is selected from the group of carboxydotrophic acetogenic bacteria.
  • the microorganism is selected from the group comprising Clostridium autoethanogenum, Clostridium ljungdahlii, Clostridium ragsdalei, Clostridium carboxidivorans, Clostridium drakei, Clostridium scatologenes, Clostridium aceticum, Clostridium formicoaceticum, Clostridium magnum, Butyribacterium methylotrophicum, Acetobacterium woodii, Alkalibaculum bacchii, Blautia producta, Eubacterium limosum, Moorella thermoacetica, Moorella thermautotrophica, Sporomusa ovata, Sporomusa silvacetica, Sporomusa sphaeroides, Oxobacter pfennigii , and Thermoanaerobacter kiuvi.
  • the parental microorganism is selected from the cluster of ethanologenic, acetogenic Clostridia comprising the species C. autoethanogenum, C. ljungdahlii , and C. ragsdalei and related isolates.
  • These include but are not limited to strains C. autoethanogenum JAI-1T (DSM10061) [Abrini J, Naria H, Nyns E- J: Clostridium autoethanogenum , sp. nov., an anaerobic bacterium that produces ethanol from carbon monoxide. Arch Microbiol 1994, 4: 345-351 ], C.
  • Clostridium coskatii [Zahn et at—Novel ethanologenic species Clostridium coskatii (US Patent Application number US20110229947)] and “ Clostridium sp.” (Tyurin et al., 2012 , J. Biotech Res. 4: 1-12), or mutated strains such as C. ljungdahlii OTA-1 (Tirado-Acevedo O. Production of Bioethanol from Synthesis Gas Using Clostridium ljungdahlii . PhD thesis, North Carolina State University, 2010).
  • rhamnose, arabinose e.g. gluconate, citrate
  • amino acids e.g. arginine, histidine
  • substrates e.g. betaine, butanol.
  • auxotroph to certain vitamins (e.g. thiamine, biotin) while others were not.
  • the parental carboxydotrophic acetogenic microorganism is selected from the group consisting of Clostridium autoethanogenum, Clostridium ljungdahlii, Clostridium ragsdalei, Clostridium carboxidivorans, Clostridium drakei, Clostridium scatologenes, Butyribacterium limosum, Butyribacterium methylotrophicum, Acetobacterium woodii, Alkalibaculum bacchii, Blautia producta, Eubacterium limosum, Moorella thermoacetica, Moorella thermautotrophica, Oxobacter pfennigii , and Thermoanaerobacter kiuvi.
  • the parental microorganism is selected from the group of carboxydotrophic Clostridia comprising Clostridium autoethanogenum, Clostridium ljungdahlii, Clostridium ragsdalei, Clostridium carboxidivorans, Clostridium drakei, Clostridium scatologenes, Clostridium aceticum, Clostridium formicoaceticum, Clostridium magnum.
  • the microorganism is selected from a cluster of carboxydotrophic Clostridia comprising the species C. autoethanogenum, C. ljungdahlii , and “ C. ragsdalei ” and related isolates. These include but are not limited to strains C. autoethanogenum JAI-1 T (DSM10061) (Abrini, Nacupunctur, & Nyns, 1994), C. autoethanogenum LBS1560 (DSM19630) (WO/2009/064200), C. autoethanogenum LBS1561 (DSM23693), C.
  • strains form a subcluster within the Clostridial rRNA cluster I (Collins et al., 1994), having at least 99% identity on 16S rRNA gene level, although being distinct species as determined by DNA-DNA reassociation and DNA fingerprinting experiments (WO 2008/028055, US patent 2011/0229947).
  • strains of this cluster are defined by common characteristics, having both a similar genotype and phenotype, and they all share the same mode of energy conservation and fermentative metabolism.
  • the strains of this cluster lack cytochromes and conserve energy via an Rnf complex.
  • strains of this cluster have a genome size of around 4.2 MBp (Köpke et al., 2010) and a GC composition of around 32% mol (Abrini et al., 1994; Köpke et al., 2010; Tanner et al., 1993) (WO 2008/028055; US patent 2011/0229947), and conserved essential key gene operons encoding for enzymes of Wood-Ljungdahl pathway (Carbon monoxide dehydrogenase, Formyl-tetrahydrofolate synthetase, Methylene-tetrahydrofolate dehydrogenase, Formyl-tetrahydrofolate cyclohydrolase, Methylene-tetrahydrofolate reductase, and Carbon monoxide dehydrogenase/Acetyl-CoA synthase), hydrogenase, formate dehydrogenase, Rnf complex (rnfCDGEAB), pyruv
  • strains all have a similar morphology and size (logarithmic growing cells are between 0.5 ⁇ 0.7 ⁇ 3-5 ⁇ m), are mesophilic (optimal growth temperature between 30-37° C.) and strictly anaerobe (Abrini et al., 1994; Tanner et al., 1993) (WO 2008/028055).
  • the traits described are therefore not specific to one organism like C. autoethanogenum or C. ljungdahlii , but rather general traits for carboxydotrophic, ethanol-synthesizing Clostridia. Thus, the invention can be anticipated to work across these strains, although there may be differences in performance.
  • the recombinant carboxydotrophic acetogenic microorganisms of the invention may be prepared from a parental carboxydotrophic acetogenic microorganism and one or more exogenous nucleic acids using any number of techniques known in the art for producing recombinant microorganisms.
  • transformation including transduction or transfection
  • transformation may be achieved by electroporation, electrofusion, ultrasonication, polyethylene glycol-mediated transformation, conjugation, or chemical and natural competence. Suitable transformation techniques are described for example in Sambrook J, Fritsch E F, Maniatis T: Molecular Cloning: A laboratory Manual, Cold Spring Harbour Labrotary Press, Cold Spring Harbour, 1989.
  • Electroporation has been described for several carboxydotrophic acetogens as C. ljungdahlii (Köpke et al., 2010; Leang, Ueki, Nevin, & Lovley, 2012) (PCT/NZ2011/000203; WO2012/053905), C. autoethanogenum (PCT/NZ2011/000203; WO2012/053905), Acetobacterium woodii (Streck, Sauer, Kuhn, & Dune, 1994) or Moorella thermoacetica (Kita et al., 2012) and is a standard method used in many Clostridia such as C.
  • acetobutylicum (Mermelstein, Welker, Bennett, & Papoutsakis, 1992), C. cellulolyticum (Jennert, Tardif, Young, & Young, 2000) or C. thermocellum (MV Tyurin, Desai, & Lynd, 2004).
  • Electrofusion has been described for acetogenic Clostridium sp. MT351 (Tyurin and Kiriukhin, 2012).
  • the parental strain uses CO as its sole carbon and energy source.
  • the parental microorganism is Clostridium autoethanogenum or Clostridium ljungdahlii .
  • the microorganism is Clostridium autoethanogenum DSM23693.
  • the microorganism is Clostridium ljungdahlii DSM13528 (or ATCC55383).
  • the invention also provides one or more nucleic acids or nucleic acid constructs of use in generating a recombinant microorganism of the invention.
  • the nucleic acid comprises sequences encoding one or more of the enzymes in the mevalonate (MVA) pathway and optionally the DXS pathway which when expressed in a microorganism allows the microorganism to produce one or more terpenes and/or precursors thereof by fermentation of a substrate comprising CO.
  • the invention provides a nucleic acid encoding two or more enzymes which when expressed in a microorganism allows the microorganism to produce one or more terpene and/or precursor thereof by fermentation of substrate comprising CO.
  • a nucleic acid of the invention encodes three, four, five or more of such enzymes.
  • the one or more enzymes encoded by the nucleic acid are from the mevalonate (MVA) pathway and are selected from the group consisting of:
  • thiolase EC 2.3.1.9
  • HMG-CoA synthase EC 2.3.3.10
  • HMG-CoA reductase EC 1.1.1.88
  • Mevalonate kinase EC 2.7.1.36
  • Phosphomevalonate kinase EC 2.7.4.2
  • f) Mevalonate Diphosphate decarboxylase EC 4.1.1.33
  • the one or more optional enzymes encoded by the nucleic acid are from the DXS pathway are selected from the group consisting of:
  • the nucleic acid encodes one or more further enzymes that are expressed or over-expressed to result in the production of a terpene compound and/or precursor thereof wherein the exogenous enzyme that is expressed, or the endogenous enzyme that is overexpressed is selected from the group consisting of:
  • geranyltranstransferase Fps (EC:2.5.1.10), b) heptaprenyl diphosphate synthase (EC:2.5.1.10), c) octaprenyl-diphosphate synthase (EC:2.5.1.90), d) isoprene synthase (EC 4.2.3.27), e) isopentenyl-diphosphate delta-isomerase (EC EC 5.3.3.2), f) farnesene synthase (EC 4.2.3.46/EC 4.2.3.47), and g) a functionally equivalent variant of any one thereof.
  • nucleic acid sequences encoding each of the above enzymes are provided herein or can be obtained from GenBank as mentioned hereinbefore.
  • skilled persons will readily appreciate alternative nucleic acid sequences encoding the enzymes or functionally equivalent variants thereof, having regard to the information contained herein, in GenBank and other databases, and the genetic code.
  • nucleic acid encoding thiolase (thIA) derived from Clostridium acetobutylicum ATCC824 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 40 hereinafter, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding thiolase wherein the thiolase is acetyl-CoA c-acetyltransferase (vraB) derived from Staphylococcus aureus subsp. aureus Mu50 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 41 hereinafter, or it is a functionally equivalent variant thereof.
  • nucleic acid encoding 3-hydroxy-3-methylglutaryl-CoA synthase (HMGS) derived from Staphylococcus aureus subsp. aureus Mu50 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 42 hereinafter, or it is a functionally equivalent variant thereof.
  • HMGS 3-hydroxy-3-methylglutaryl-CoA synthase
  • the nucleic acid encoding Hydroxymethylglutaryl-CoA reductase (HMGR) derived from Staphylococcus aureus subsp. aureus Mu50 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 43 hereinafter, or it is a functionally equivalent variant thereof.
  • HMGR Hydroxymethylglutaryl-CoA reductase
  • the nucleic acid encoding mevalonate kinase (MK) derived from Staphylococcus aureus subsp. aureus Mu50 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 51 hereinafter, or it is a functionally equivalent variant thereof.
  • nucleic acid encoding phosphomevalonate kinase (PMK) derived from Staphylococcus aureus subsp. aureus Mu50 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 52 hereinafter, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding mevalonate diphosphate decarboxylase (PMD) derived from Staphylococcus aureus subsp. aureus Mu50 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 53 hereinafter, or it is a functionally equivalent variant thereof.
  • PMD mevalonate diphosphate decarboxylase
  • nucleic acid encoding deoxyxylulose 5-phosphate synthase derived from C. autoethanogenum is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 1 and/or with the amino acid sequence exemplified in SEQ ID NO: 2 hereinafter, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding 1-deoxy-D-xylulose 5-phosphate reductoisomerase DXR (EC:1.1.1.267) has the sequence SEQ ID NO: 3 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase IspD (EC:2.7.7.60) has the sequence SEQ ID NO: 5 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase IspE (EC:2.7.1.148) has the sequence SEQ ID NO: 7 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase IspF (EC:4.6.1.12) has the sequence SEQ ID NO: 9 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase IspG (EC:1.17.7.1) has the sequence SEQ ID NO: 11 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding 4-hydroxy-3-methylbut-2-enyl diphosphate reductase (EC:1.17.1.2) has the sequence SEQ ID NO: 13 or is a functionally equivalent variant thereof.
  • the nucleic acid encoding Geranyltranstransferase (ispA) derived from Escherichia coli str. K-12 substr. MG1655 is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 56 hereinafter, or it is a functionally equivalent variant thereof.
  • the nucleic acid encoding heptaprenyl diphosphate synthase has the sequence SEQ ID NO: 17, or it is a functionally equivalent variant thereof.
  • nucleic acid encoding octaprenyl-diphosphate synthase (EC:2.5.1.90) wherein the octaprenyl-diphosphate synthase is polyprenyl synthetase is encoded by sequence SEQ ID NO: 19, or it is a functionally equivalent variant thereof.
  • nucleic acid encoding isoprene synthase (ispS) derived from Poplar tremuloides is exemplified in SEQ ID NO: 21 hereinafter, or it is a functionally equivalent variant thereof.
  • nucleic acid encoding Isopentenyl-diphosphate delta-isomerase (idi) derived from Clostridium beijerinckii is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 54 hereinafter, or it is a functionally equivalent variant thereof.
  • nucleic acid encoding Alpha-farnesene synthase (FS) derived from Malus ⁇ domestica is encoded by the nucleic acid sequence exemplified in SEQ ID NO: 57 hereinafter, or it is a functionally equivalent variant thereof.
  • the nucleic acids of the invention will further comprise a promoter.
  • the promoter allows for constitutive expression of the genes under its control.
  • inducible promoters may also be employed. Persons of skill in the art will readily appreciate promoters of use in the invention.
  • the promoter can direct a high level of expression under appropriate fermentation conditions.
  • a Wood-Ljungdahl cluster promoter is used.
  • a Phosphotransacetylase/Acetate kindase promoter is used.
  • the promoter is from C. autoethanogenum.
  • nucleic acids of the invention may remain extra-chromosomal upon transformation of a parental microorganism or may be adapted for intergration into the genome of the microorganism. Accordingly, nucleic acids of the invention may include additional nucleotide sequences adapted to assist integration (for example, a region which allows for homologous recombination and targeted integration into the host genome) or stable expression and replication of an extrachromosomal construct (for example, origin of replication, promoter and other regulatory sequences).
  • the nucleic acid is nucleic acid construct or vector.
  • the nucleic acid construct or vector is an expression construct or vector, however other constructs and vectors, such as those used for cloning are encompassed by the invention.
  • the expression construct or vector is a plasmid.
  • an expression construct/vector of the present invention may contain any number of regulatory elements in addition to the promoter as well as additional genes suitable for expression of further proteins if desired.
  • the expression construct/vector includes one promoter.
  • the expression construct/vector includes two or more promoters.
  • the expression construct/vector includes one promoter for each gene to be expressed.
  • the expression construct/vector includes one or more ribosomal binding sites, preferably a ribosomal binding site for each gene to be expressed.
  • nucleic acid sequences and construct/vector sequences described herein may contain standard linker nucleotides such as those required for ribosome binding sites and/or restriction sites. Such linker sequences should not be interpreted as being required and do not provide a limitation on the sequences defined.
  • Nucleic acids and nucleic acid constructs may be constructed using any number of techniques standard in the art. For example, chemical synthesis or recombinant techniques may be used. Such techniques are described, for example, in Sambrook et al (Molecular Cloning: A laboratory manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989). Further exemplary techniques are described in the Examples section herein after. Essentially, the individual genes and regulatory elements will be operably linked to one another such that the genes can be expressed to form the desired proteins. Suitable vectors for use in the invention will be appreciated by those of ordinary skill in the art. However, by way of example, the following vectors may be suitable: pMTL80000 vectors, pIMP1, pJIR750, and the plasmids exemplified in the Examples section herein after.
  • nucleic acids of the invention may be in any appropriate form, including RNA, DNA, or cDNA.
  • the invention also provides host organisms, particularly microorganisms, and including viruses, bacteria, and yeast, comprising any one or more of the nucleic acids described herein.
  • the one or more exogenous nucleic acids may be delivered to a parental microorganism as naked nucleic acids or may be formulated with one or more agents to facilitate the transformation process (for example, liposome-conjugated nucleic acid, an organism in which the nucleic acid is contained).
  • the one or more nucleic acids may be DNA, RNA, or combinations thereof, as is appropriate. Restriction inhibitors may be used in certain embodiments; see, for example Murray, N. E. et al. (2000) Microbial. Molec. Biol. Rev. 64, 412.)
  • the microorganisms of the invention may be prepared from a parental microorganism and one or more exogenous nucleic acids using any number of techniques known in the art for producing recombinant microorganisms.
  • transformation including transduction or transfection
  • transformation may be achieved by electroporation, ultrasonication, polyethylene glycol-mediated transformation, chemical or natural competence, or conjugation.
  • Suitable transformation techniques are described for example in, Sambrook J, Fritsch E F, Maniatis T: Molecular Cloning: A laboratory Manual, Cold Spring Harbour Labrotary Press, Cold Spring Harbour, 1989.
  • methylate the nucleic acid to be introduced into the microorganism due to the restriction systems which are active in the microorganism to be transformed, it is necessary to methylate the nucleic acid to be introduced into the microorganism. This can be done using a variety of techniques, including those described below, and further exemplified in the Examples section herein after.
  • a recombinant microorganism of the invention is produced by a method comprises the following steps:
  • the methyltransferase gene of step B is expressed constitutively.
  • step B expression of the methyltransferase gene of step B is induced.
  • the shuttle microorganism is a microorganism, preferably a restriction negative microorganism, that facilitates the methylation of the nucleic acid sequences that make up the expression construct/vector.
  • the shuttle microorganism is a restriction negative E. coli, Bacillus subtillis , or Lactococcus lactis.
  • the methylation construct/vector comprises a nucleic acid sequence encoding a methyltransferase.
  • the methyltransferase gene present on the methylation construct/vector is induced.
  • Induction may be by any suitable promoter system although in one particular embodiment of the invention, the methylation construct/vector comprises an inducible lac promoter and is induced by addition of lactose or an analogue thereof, more preferably isopropyl- ⁇ -D-thio-galactoside (IPTG).
  • suitable promoters include the ara, tet, or T7 system.
  • the methylation construct/vector promoter is a constitutive promoter.
  • the methylation construct/vector has an origin of replication specific to the identity of the shuttle microorganism so that any genes present on the methylation construct/vector are expressed in the shuttle microorganism.
  • the expression construct/vector has an origin of replication specific to the identity of the destination microorganism so that any genes present on the expression construct/vector are expressed in the destination microorganism.
  • the expression construct/vector may then be isolated from the shuttle microorganism according to any one of a number of known methods. By way of example only, the methodology described in the Examples section described hereinafter may be used to isolate the expression construct/vector.
  • both construct/vector are concurrently isolated.
  • the expression construct/vector may be introduced into the destination microorganism using any number of known methods. However, by way of example, the methodology described in the Examples section hereinafter may be used. Since the expression construct/vector is methylated, the nucleic acid sequences present on the expression construct/vector are able to be incorporated into the destination microorganism and successfully expressed.
  • a methyltransferase gene may be introduced into a shuttle microorganism and over-expressed.
  • the resulting methyltransferase enzyme may be collected using known methods and used in vitro to methylate an expression plasmid.
  • the expression construct/vector may then be introduced into the destination microorganism for expression.
  • the methyltransferase gene is introduced into the genome of the shuttle microorganism followed by introduction of the expression construct/vector into the shuttle microorganism, isolation of one or more constructs/vectors from the shuttle microorganism and then introduction of the expression construct/vector into the destination microorganism.
  • the expression construct/vector and the methylation construct/vector as defined above may be combined to provide a composition of matter.
  • Such a composition has particular utility in circumventing restriction barrier mechanisms to produce the recombinant microorganisms of the invention.
  • the expression construct/vector and/or the methylation construct/vector are plasmids.
  • methyltransferases of use in producing the microorganisms of the invention.
  • Bacillus subtilis phage ⁇ T1 methyltransferase and the methyltransferase described in the Examples herein after may be used.
  • the methyltransferase has the amino acid sequence of SEQ ID NO: 60 or is a functionally equivalent variant thereof.
  • Nucleic acids encoding suitable methyltransferases will be readily appreciated having regard to the sequence of the desired methyltransferase and the genetic code.
  • the nucleic acid encoding a methyltransferase is as described in the Examples herein after (for example the nucleic acid of SEQ ID NO: 63, or it is a functionally equivalent variant thereof).
  • any number of constructs/vectors adapted to allow expression of a methyltransferase gene may be used to generate the methylation construct/vector.
  • the plasmid described in the Examples section hereinafter may be used.
  • the invention provides a method for the production of one or more terpenes and/or precursors thereof, and optionally one or more other products, by microbial fermentation comprising fermenting a substrate comprising CO using a recombinant microorganism of the invention.
  • the one or more terpene and/or precursor thereof is the main fermentation product.
  • the methods of the invention may be used to reduce the total atmospheric carbon emissions from an industrial process.
  • the fermentation comprises the steps of anaerobically fermenting a substrate in a bioreactor to produce at least one or more terpenes and/or a precursor thereof using a recombinant microorganism of the invention.
  • the one or more terpene and/or precursor thereof is chosen from mevalonic acid, IPP, dimethylallyl pyrophosphate (DMAPP), isoprene, geranyl pyrophosphate (GPP), farnesyl pyrophosphate (FPP) and farnesene.
  • DMAPP dimethylallyl pyrophosphate
  • GPP geranyl pyrophosphate
  • FPP farnesyl pyrophosphate
  • the gaseous substrate fermented by the microorganism is a gaseous substrate containing CO.
  • the gaseous substrate may be a CO-containing waste gas obtained as a by-product of an industrial process, or from some other source such as from automobile exhaust fumes.
  • the industrial process is selected from the group consisting of ferrous metal products manufacturing, such as a steel mill, non-ferrous products manufacturing, petroleum refining processes, gasification of coal, electric power production, carbon black production, ammonia production, methanol production and coke manufacturing.
  • the CO-containing gas may be captured from the industrial process before it is emitted into the atmosphere, using any convenient method.
  • the CO may be a component of syngas (gas comprising carbon monoxide and hydrogen).
  • syngas gas comprising carbon monoxide and hydrogen.
  • the CO produced from industrial processes is normally flared off to produce CO 2 and therefore the invention has particular utility in reducing CO 2 greenhouse gas emissions and producing a terpene for use as a biofuel.
  • the gaseous substrate may be filtered or scrubbed using known methods.
  • a suitable liquid nutrient medium will need to be fed to the bioreactor.
  • the substrate and media may be fed to the bioreactor in a continuous, batch or batch fed fashion.
  • a nutrient medium will contain vitamins and minerals sufficient to permit growth of the micro-organism used.
  • Anaerobic media suitable for fermentation to produce a terpene and/or a prescursor thereof using CO are known in the art.
  • suitable media are described Biebel (2001). In one embodiment of the invention the media is as described in the Examples section herein after.
  • the fermentation should desirably be carried out under appropriate conditions for the CO-to-the at least one or more terpene and/or precursor thereof fermentation to occur.
  • Reaction conditions that should be considered include pressure, temperature, gas flow rate, liquid flow rate, media pH, media redox potential, agitation rate (if using a continuous stirred tank reactor), inoculum level, maximum gas substrate concentrations to ensure that CO in the liquid phase does not become limiting, and maximum product concentrations to avoid product inhibition.
  • reactor volume can be reduced in linear proportion to increases in reactor operating pressure, i.e. bioreactors operated at 10 atmospheres of pressure need only be one tenth the volume of those operated at 1 atmosphere of pressure.
  • WO 02/08438 describes gas-to-ethanol fermentations performed under pressures of 30 psig and 75 psig, giving ethanol productivities of 150 g/l/day and 369 g/l/day respectively.
  • example fermentations performed using similar media and input gas compositions at atmospheric pressure were found to produce between 10 and 20 times less ethanol per litre per day.
  • the rate of introduction of the CO-containing gaseous substrate is such as to ensure that the concentration of CO in the liquid phase does not become limiting. This is because a consequence of CO-limited conditions may be that one or more product is consumed by the culture.
  • the composition of gas streams used to feed a fermentation reaction can have a significant impact on the efficiency and/or costs of that reaction.
  • O2 may reduce the efficiency of an anaerobic fermentation process. Processing of unwanted or unnecessary gases in stages of a fermentation process before or after fermentation can increase the burden on such stages (e.g. where the gas stream is compressed before entering a bioreactor, unnecessary energy may be used to compress gases that are not needed in the fermentation). Accordingly, it may be desirable to treat substrate streams, particularly substrate streams derived from industrial sources, to remove unwanted components and increase the concentration of desirable components.
  • a culture of a bacterium of the invention is maintained in an aqueous culture medium.
  • the aqueous culture medium is a minimal anaerobic microbial growth medium.
  • Suitable media are known in the art and described for example in U.S. Pat. Nos. 5,173,429 and 5,593,886 and WO 02/08438, and as described in the Examples section herein after.
  • Terpenes and/or precursors thereof may be recovered from the fermentation broth by methods known in the art, such as fractional distillation or evaporation, pervaporation, gas stripping and extractive fermentation, including for example, liquid-liquid extraction.
  • the one or more terpene and/or precursor thereof and one or more products are recovered from the fermentation broth by continuously removing a portion of the broth from the bioreactor, separating microbial cells from the broth (conveniently by filtration), and recovering one or more products from the broth.
  • Alcohols may conveniently be recovered for example by distillation.
  • Acetone may be recovered for example by distillation.
  • Any acids produced may be recovered for example by adsorption on activated charcoal.
  • the separated microbial cells are preferably returned to the fermentation bioreactor.
  • the cell free permeate remaining after any alcohol(s) and acid(s) have been removed is also preferably returned to the fermentation bioreactor. Additional nutrients (such as B vitamins) may be added to the cell free permeate to replenish the nutrient medium before it is returned to the bioreactor.
  • the pH of the broth was adjusted as described above to enhance adsorption of acetic acid to the activated charcoal, the pH should be re-adjusted to a similar pH to that of the broth in the fermentation bioreactor, before being returned to the bioreactor.
  • the inventors have identified terpene biosynthesis genes in carboxydotrophic acetogens such as C. autoethanogenum and C. ljungdahlii .
  • a recombinant organism was engineered to produce isoprene. Isoprene is naturally emitted by some plant such as poplar to protect its leave from UV radiation.
  • Isoprene synthase (EC 4.2.3.27) gene of Poplar was codon optimized and introduced into a carboxydotrophic acetogen C. autoethanogenum to produce isoprene from CO.
  • the enzyme takes key intermediate DMAPP (Dimethylallyl diphosphate) of terpenoid biosynthesis to isoprene in an irreversible reaction ( FIG. 1 ).
  • DMAPP Dimethylallyl diphosphate
  • DSM10061 and DSM23693 were obtained from DSMZ (The German Collection of Microorganisms and Cell Cultures, Inhoffenstra ⁇ e 7 B, 38124 Braunschweig, Germany). Growth was carried out at 37° C. using strictly anaerobic conditions and techniques (Hungate, 1969, Methods in Microbiology, vol. 3B. Academic Press, New York: 117-132; Wolfe, 1971 , Adv. Microb. Physiol., 6: 107-146).
  • PETC media without yeast extract (Table 1) and 30 psi carbon monoxide containing steel mill waste gas (collected from New Zealand Steel site in Glenbrook, NZ; composition: 44% CO, 32% N 2 , 22% CO 2 , 2% H 2 ) as sole carbon and energy source was used.
  • Genomic DNA from Clostridium autoethanogenum DSM23693 was isolated using a modified method by Bertram and Dune (1989). A 100-ml overnight culture was harvested (6,000 ⁇ g, 15 min, 4° C.), washed with potassium phosphate buffer (10 mM, pH 7.5) and suspended in 1.9 ml STE buffer (50 mM Tris-HCl, 1 mM EDTA, 200 mM sucrose; pH 8.0). 300 ⁇ l lysozyme ( ⁇ 100,000 U) was added and the mixture was incubated at 37° C. for 30 min, followed by addition of 280 ⁇ l of a 10% (w/v) SDS solution and another incubation for 10 min.
  • the Pyruvate:ferredoxin oxidoreductase promoter sequence was amplified by PCR using oligonucleotides Ppfor-NotI-F (SEQ ID NO: 23: AAGCGGCCGCAAAATAGTTGATAATAATGC) and Ppfor-NdeI-R (SEQ ID NO: 24: TACGCATATGAATTCCTCTCCTTTTCAAGC) using iProof High Fidelity DNA Polymerase (Bio-Rad Laboratories) and the following program: initial denaturation at 98° C. for 30 seconds, followed by 32 cycles of denaturation (98° C. for 10 seconds), annealing (50-62° C. for 30-120 seconds) and elongation (72° C. for 30-90 seconds), before a final extension step (72° C. for 10 minutes).
  • Ppfor-NotI-F SEQ ID NO: 23: AAGCGGCCGCAAAATAGTTGATAATAATGC
  • Ppfor-NdeI-R SEQ ID
  • E. coli DH5 ⁇ -T1 R Invitrogen
  • XL 1-Blue MRF′ Kan (Stratagene).
  • the amplified P pfor promoter region was cloned into the E. coli - Clostridium shuttle vector pMTL85141 (FJ797651.1; Nigel Minton, University of Nottingham; Heap et al., 2009) using NotI and NdeI restriction sites, generating plasmid pMTL85146.
  • ispS was cloned into pMTL85146 using restriction sites NdeI and EcoRI, resulting in plasmid pMTL 85146-ispS ( FIG. 2 , SEQ ID NO: 25).
  • DNA Prior to transformation, DNA was methylated in vivo in E. coli using a synthesized hybrid Type II methyltransferase (SEQ ID NO: 63) co-expressed on a methylation plasmid (SEQ ID NO: 64) designed from methyltransferase genes from C. autoethanogenum, C. ragsdalei and C. ljungdahlii as described in US patent 2011/0236941.
  • Both expression plasmid and methylation plasmid were transformed into same cells of restriction negative E. coli XL1-Blue MRF′ Kan (Stratagene), which is possible due to their compatible Gram-( ⁇ ) origins of replication (high copy ColE1 in expression plasmid and low copy p15A in methylation plasmid).
  • In vivo methylation was induced by addition of 1 mM IPTG, and methylated plasmids were isolated using QIAGEN Plasmid Midi Kit (QIAGEN). The resulting mixture was used for transformation experiments with C. autoethanogenum DSM23693, but only the abundant (high-copy) expression plasmid has a Gram-(+) replication origin (repL) allowing it to replicate in Clostridia.
  • C. autoethanogenum DSM23693 was grown in PETC media (Table 1) supplemented with 1 g/L yeast extract and 10 g/l fructose as well as 30 psi steel mill waste gas (collected from New Zealand Steel site in Glenbrook, NZ; composition: 44% CO, 32% N 2 , 22% CO 2 , 2% H 2 ) as carbon source.
  • a 50 ml culture of C. autoethanogenum DSM23693 was subcultured to fresh media for 3 consecutive days. These cells were used to inoculate 50 ml PETC media containing 40 mM DL-threonine at an OD 600nm of 0.05. When the culture reached an OD 600nm of 0.4, the cells were transferred into an anaerobic chamber and harvested at 4,700 ⁇ g and 4° C. The culture was twice washed with ice-cold electroporation buffer (270 mM sucrose, 1 mM MgCl 2 , 7 mM sodium phosphate, pH 7.4) and finally suspended in a volume of 600 ⁇ l fresh electroporation buffer.
  • ice-cold electroporation buffer 270 mM sucrose, 1 mM MgCl 2 , 7 mM sodium phosphate, pH 7.4
  • This mixture was transferred into a pre-cooled electroporation cuvette with a 0.4 cm electrode gap containing 1 ⁇ g of the methylated plasmid mixture and immediately pulsed using the Gene pulser Xcell electroporation system (Bio-Rad) with the following settings: 2.5 kV, 600 ⁇ , and 25 ⁇ F. Time constants of 3.7-4.0 ms were achieved.
  • the culture was transferred into 5 ml fresh media. Regeneration of the cells was monitored at a wavelength of 600 nm using a Spectronic Helios Epsilon Spectrophotometer (Thermo) equipped with a tube holder. After an initial drop in biomass, the cells started growing again.
  • the cells were harvested, suspended in 200 ⁇ l fresh media and plated on selective PETC plates (containing 1.2% BactoTM Agar (BD)) with appropriate antibiotics 4 ⁇ g/ml Clarithromycin or 15 ⁇ g/ml thiamphenicol. After 4-5 days of inoculation with 30 psi steel mill gas at 37° C., colonies were visible.
  • BD BactoTM Agar
  • the colonies were used to inoculate 2 ml PETC media with antibiotics. When growth occurred, the culture was scaled up into a volume of 5 ml and later 50 ml with 30 psi steel mill gas as sole carbon source.
  • a plasmid mini prep was performed from 10 ml culture volume using Zyppy plasmid miniprep kit (Zymo). Since the quality of the isolated plasmid was not sufficient for a restriction digest due to Clostridial exonuclease activity [Burchhardt and Dune, 1990], a PCR was performed with the isolated plasmid with oligonucleotide pairs colE1-F (SEQ ID NO: 65: CGTCAGACCCCGTAGAAA) plus colE1-R (SEQ ID NO: 66: CTCTCCTGTTCCGACCCT).
  • PCR was carried out using iNtRON Maximise Premix PCR kit (Intron Bio Technologies) with the following conditions: initial denaturation at 94° C. for 2 minutes, followed by 35 cycles of denaturation (94° C. for 20 seconds), annealing (55° C. for 20 seconds) and elongation (72° C. for 60 seconds), before a final extension step (72° C. for 5 minutes).
  • genomic DNA was isolated (see above) from 50 ml cultures of C. autoethanogenum DSM23693.
  • a PCR was performed against the 16s rRNA gene using oligonucleotides fD1 (SEQ ID NO: 67: CCGAATTCGTCGACAACAGAGTTTGATCCTGGCTCAG) and rP2 (SEQ ID NO: 68: CCCGGGATCCAAGCTTACGGCTACCTTGTTACGACTT) [Weisberg et al., 1991] and iNtRON Maximise Premix PCR kit (Intron Bio Technologies) with the following conditions: initial denaturation at 94° C. for 2 minutes, followed by 35 cycles of denaturation (94° C.
  • Sequencing results were at least 99.9% identity against the 16s rRNA gene (rrsA) of C. autoethanogenum (Y18178, GI:7271109).
  • a culture harboring isoprene synthase plasmid pMTL 85146-ispS and a control culture without plasmid was grown in 50 mL serum bottles and PETC media (Table 1) with 30 psi steel mill waste gas (collected from New Zealand Steel site in Glenbrook, NZ; composition: 44% CO, 32% N 2 , 22% CO 2 , 2% H 2 ) as sole energy and carbon source.
  • 0.8 mL samples were taken during logarithmic growth phase at an OD 600nm of around 0.5 and mixed with 1.6 mL RNA protect reagent (Qiagen).
  • a melting-curve analysis was performed immediately after completion of the qPCR (38 cycles of 58° C. to 95° C. at 1° C./s).
  • Two housekeeping genes (guanylate kinase and formate tetrahydrofolate ligase) were included for each cDNA sample for normalization. Determination of relative gene expression was conducted using Relative Expression Software Tool (REST ⁇ ) 2008 V2.0.7 (38). Dilution series of cDNA spanning 4 log units were used to generate standard curves and the resulting amplification efficiencies to calculate concentration of mRNA.
  • DMAPP Dimethylallyl diphosphate
  • IPP Isopentenyl diphosphate
  • Isopentenyl-diphosphate delta-isomerase gene idi from C. beijerinckii (Gene ID:5294264), encoding an Isopentenyl-diphosphate delta-isomerase (YP — 001310174.1), was cloned downstream of ispS.
  • the gene was amplified using oligonucleotide Idi-Cbei-SacI-F (SEQ ID NO: 26: GTGAGCTCGAAAGGGGAAATTAAATG) and Idi-Cbei-KpnI-R (SEQ ID NO: 27: ATGGTACCCCAAATCTTTATTTAGACG) from genomic DNA of C.
  • the PCR product was cloned into vector pMTL 85146-ispS using Sad and KpnI restriction sites to yield plasmid pMTL85146-ispS-idi (SEQ ID NO: 28).
  • the antibiotic resistance marker was exchanged from catP to ermB (released from vector pMTL82254 (FJ797646.1; Nigel Minton, University of Nottingham; Heap et al., 2009) using restriction enzymes PmeI and FseI to form plasmid pMTL85246-ispS-idi ( FIG. 3 ).
  • Transformation and expression in C. autoethanogenum was carried out as described for plasmid pMTL 85146-ispS. After successful transformation, growth experiment was carried out in 50 mL 50 mL serum bottles and PETC media (Table 1) with 30 psi steel mill waste gas (collected from New Zealand Steel site in Glenbrook, NZ; composition: 44% CO, 32% N 2 , 22% CO 2 , 2% H 2 ) as sole energy and carbon source. To confirm that the plasmid has been successfully introduced, plasmid mini prep DNA was carried out from transformants as described previously.
  • colE1-F SEQ ID NO: 65: CGTCAGACCCCGTAGAAA and colE1-R: SEQ ID NO: 66: CTCTCCTGTTCCGACCCT
  • ermB SEQ ID NO: 106: TTTGTAATTAAGAAGGAG
  • ermB-R SEQ ID NO: 107: GTAGAATCCTTCTTCAAC
  • idi Idi-Cbei-SacI-F: SEQ ID NO: 26: GTGAGCTCGAAAGGGGAAATTAAATG and Idi-Cbei-KpnI-R: SEQ ID NO: 27: ATGGTACCCCAAATCTTTATTTAGACG
  • DXS deoxyxylulose 5-phosphate synthase
  • the dxs gene of C. autoethanogenum was amplified from genomic DNA with oligonucleotides Dxs-SalI-F (SEQ ID NO: 29: GCAGTCGACTTTATTAAAGGGATAGATAA) and Dxs-XhoI-R (SEQ ID NO: 30: TGCTCGAGTTAAAATATATGACTTACCTCTG) as described for other genes above.
  • the amplified gene was then cloned into plasmid pMTL85246-ispS-idi with SalI and XhoI to produce plasmid pMTL85246-ispS-idi-dxs (SEQ ID NO: 31 and FIG. 4 ).
  • Oligonucleotide pair dxs-F (SEQ ID NO: 73: ACAAAGTATCTAAGACAGGAGGTCA) and dxs-R (SEQ ID NO: 74: GATGTCCCACATCCCATATAAGTTT) was used to measure expression of gene dxs in both wild-type strain and strain carrying plasmid pMTL 85146-ispS-idi-dxs. mRNA levels in the strain carrying the plasmid were found to be over 3 times increased compared to the wild-type ( FIG. 15 ). Biomass was normalized before RNA extraction.
  • the first step of the mevalonate pathway ( FIG. 7 ) is catalyzed by a thiolase that converts two molecules of acetyl-CoA into acetoacetyl-CoA (and HS-CoA).
  • This enzyme has been successfully expressed in carboxydotrophic acetogens Clostridium autoethanogenum and C. ljungdahlii by the same inventors (US patent 2011/0236941). Constructs for the remaining genes of the mevalonate pathway have been designed.
  • Phosphotransacetylase/Acetate kinase operon promoter (P pta-ack ) of C The Phosphotransacetylase/Acetate kinase operon promoter (P pta-ack ) of C.
  • autoethanogenum (SEQ ID NO: 61) was used for expression of the thiolase and HMG-CoA synthase while a promoter region of the ATP synthase (P atp ) of C. autoethanogenum was used for expression of the HMG-CoA reductase.
  • Two variants of thiolase, thlA from Clostridium acetobutylicum and vraB from Staphylococcus aureus were synthesised and flanked by NdeI and EcoRI restriction sites for further sub-cloning.
  • HMG-CoA synthase HMGS
  • HMG-CoA reductase HMGR
  • aureus 42 methylglutaryl-CoA Mu50; NC_002758.2; region: synthase (HMGS) 2689180..2690346; including GI: 15925536 Hydroxymethyl- Staphylococcus aureus subsp. aureus 43 glutaryl-CoA Mu50; NC_002758.2; region: reductase (HMGR) complement(2687648..2688925); including GI: 15925535 Phospho- Clostridium autoethanogenum DSM10061 44 transacetylase- acetate kinase operon (P pta-ack ) ATP synthase Clostridium autoethanogenum DSM10061 45 promoter (P atp )
  • the ATP synthase promoter (P atp ) together with the hydroxymethylglutaryl-CoA reductase (HMGR) was amplified using oligonucleotides pUC57-F (SEQ ID NO: 46: AGCAGATTGTACTGAGAGTGC) and pUC57-R (SEQ ID NO: 47: ACAGCTATGACCATGATTACG) and pUC57-Patp-HMGR as a template.
  • the 2033 bp amplified fragment was digested with Sad and XbaI and ligated into the E.
  • HMGS 3-hydroxy-3-methylglutaryl-CoA synthase
  • the created plasmid pMTL 82151-HMGS-Patp-HMGR (SEQ ID NO: 79) and the 1768 bp codon-optimised operon of P ptaack -thlA/vraB were both cut with NotI and EcoRI.
  • a ligation was performed and subsequently transformed into E. coli XL1-Blue MRF′ Kan resulting in plasmid pMTL8215-P ptaack -thlA/vraB-HMGS-P atp -HMGR (SEQ ID NO: 50).
  • mevalonate kinase (MK), phosphomevalonate kinase (PMK), mevalonate diphosphate decarboxylase (PMD), isopentenyl-diphosphate delta-isomerase (idi) and isoprene synthase (ispS) were codon-optimised by ATG:Biosynthetics GmbH (Merzhausen, Germany).
  • Mevalonate kinase (MK), phosphomevalonate kinase (PMK) and mevalonate diphosphate decarboxylase (PMD) were obtained from Staphylococcus aureus.
  • the promoter region of the RNF Complex (P rnf ) of C. autoethanogenum (SEQ ID NO: 62) was used for expression of mevalonate kinase (MK), phosphomevalonate kinase (PMK) and mevalonate diphosphate decarboxylase (PMD), while the promoter region of the Pyruvate:ferredoxin oxidoreductase (P for ) of C. autoethanogenum (SEQ ID NO: 22) was used for expression of isopentenyl-diphosphate delta-isomerase (idi) and isoprene synthase (ispS). All DNA sequences used are given in Table 5.
  • Prnf-MK The codon-optimised Prnf-MK was amplified from the synthesised plasmid pGH-Prnf-MK-PMK-PMD with oligonucleotides NotI-XbaI-Prnf-MK F (SEQ ID NO: 80: ATGCGCGGCCGCTAGGTCTAGAATATCGATACAGATAAAAAAATATATAATACA G) and SalI-Prnf-MK R (SEQ ID NO: 81: TGGTTCTGTAACAGCGTATTCACCTGC).
  • the amplified gene was then cloned into plasmid pMTL83145 (SEQ ID NO: 49) with NotI and SalI to produce plasmid pMTL8314-Prnf-MK (SEQ ID NO: 82).
  • This resulting plasmid and the 2165 bp codon optimised fragment PMK-PMD was subsequently digested with SalI and HindIII.
  • a ligation was performed resulting in plasmid pMTL 8314-Prnf-MK-PMK-PMD (SEQ ID NO: 83).
  • the isoprene expression plasmid without the mevalonate pathway was created by ligating the isoprene synthase (ispS) flanked by restriction sites AgeI and NheI to the previously created farnesene plasmid, pMTL 8314-Prnf-MK-PMK-PMD-Pfor-idi-ispA-FS (SEQ ID NO:91) to result in plasmid pMTL8314-Prnf-MK-PMK-PMD-Pfor-idi-ispS (SEQ ID NO:84).
  • geranyltranstransferase (ispA) was obtained from Escherichia coli str. K-12 substr. MG1655 and alpha-farnesene synthase (FS) was obtained from Malus ⁇ domestica . All DNA sequences used are given in Table 6.
  • the codon-optimised idi was amplified from the synthesised plasmid pMTL83245-Pfor-FS-idi (SEQ ID NO: 85) with via the mevalonate pathways idi_F (SEQ ID NO: 86: AGGCACTCGAGATGGCAGAGTATATAATAGCAGTAG) and idi R2 (SEQ ID NO:87: AGGCGCAAGCTTGGCGCACCGGTTTATTTAAATATCTTATTTTCAGC).
  • the amplified gene was then cloned into plasmid pMTL83245-Pfor with XhoI and HindIII to produce plasmid pMTL83245-Pfor-idi (SEQ ID NO: 88).
  • This resulting plasmid and the 1754 bp codon optimised fragment of farnesene synthase (FS) was subsequently digested with HindIII and NheI.
  • a ligation was performed resulting in plasmid pMTL83245-Pfor-idi-FS (SEQ ID NO: 89).
  • the 946 bp fragment of ispA and pMTL83245-Pfor-idi-FS was subsequently digested with AgeI and HindIII and ligated to create the resulting plasmid pMTL83245-Pfor-idi-ispA-FS (SEQ ID NO: 90).
  • the farnesene expression plasmid without the upper mevalonate pathway was created by ligating the 2516 bp fragment of Pfor-idi-ispA-FS from pMTL83245-Pfor-idi-ispA-FS to pMTL 8314-Prnf-MK-PMK-PMD to result in plasmid pMTL 8314-Prnf-MK-PMK-PMD-Pfor-idi-ispA-FS (SEQ ID NO: 91).
  • Mevalonate kinase (MK SEQ ID NO: 51), Phosphomevalonate Kinase (PMK SEQ ID NO: 52), Mevalonate Diphosphate Decarboxylase (PMD SEQ ID NO: 53), Isopentyl-diphosphate
  • Delta-isomerase (idi; SEQ ID NO: 54), Geranyltranstransferase (ispA; SEQ ID NO: 56) and Farnesene synthase (FS SEQ ID NO: 57) was done as described above in example 1. Using oligonucleotides listed in table 7.
  • Mevalonate kinase MK-RTPCR-F GTGCTGGTAGAGGTGGTTCA 94 MK-RTPCR-R CCAAGTATGTGCTGCACCAG 95 Phosphomevalonate PMK-RTPCR-F ATATCAGACCCACACGCAGC 96 Kinase PMK-RTPCR-R AATGCTTCATTGCTATGTCACATG 97 Mevalonate PMD-RTPCR- GCAGAAGCAAAGGCAGCAAT 98 Diphosphate F Decarboxylase PMD-RTPCR- TTGATCCAAGATTTGTAGCATGC 99 R Isopentyl-diphosphate idi-RTPCR-F GGACAAACACTTGTTGTAGTCACC 100 Delta-isomerase idi-RTPCR-R TCAAGTTCGCAAGTAAATCCCA 101 Geranyltranstransferase ispA-RTPCR-F ACCAGCAATGGATGACGATG 102 ispA-RTPCR-R AGTTTGTAAAGCG
  • Mevalonate kinase MK SEQ ID NO: 51
  • PMK SEQ ID NO: 52 Phosphomevalonate Kinase
  • PMD SEQ ID NO: 53 Mevalonate Diphosphate Decarboxylase
  • idi SEQ ID NO: 54 Isopentyl-diphosphate Delta-isomerase
  • Geranyltranstransferase ispA SEQ ID NO: 56
  • Farnesene synthase FS SEQ ID NO: 57
  • FIG. 17 shows a representative growth curve for 2 control cultures and two cultures fed 1 mM mevalonate. Farnesene was detected in the samples taken at 66 h and 90 h after start of experiment ( FIG. 19-21 ).

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US11459589B2 (en) 2022-10-04
US10913958B2 (en) 2021-02-09
PL3346008T3 (pl) 2021-04-19
JP6643083B2 (ja) 2020-02-12
WO2013180584A1 (fr) 2013-12-05
EP2855662B1 (fr) 2018-03-21
DK2855662T3 (en) 2018-06-25
EP3346008A1 (fr) 2018-07-11
CN104822823A (zh) 2015-08-05
US20210062229A1 (en) 2021-03-04
CN104822823B8 (zh) 2020-05-22
EP3346008B1 (fr) 2020-10-07
EP3795680A1 (fr) 2021-03-24
CN104822823B (zh) 2020-02-14
CN111218418A (zh) 2020-06-02
EA201492206A1 (ru) 2015-09-30
IN2014DN10236A (fr) 2015-08-07
ES2674984T3 (es) 2018-07-05
US20230013524A1 (en) 2023-01-19
PL2855662T3 (pl) 2018-08-31
US20150191747A1 (en) 2015-07-09
EA028892B1 (ru) 2018-01-31
JP2018110584A (ja) 2018-07-19
US20180142265A1 (en) 2018-05-24
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JP6636550B2 (ja) 2020-01-29
EP2855662A4 (fr) 2015-12-30

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