CN112251456A - Method for improving lincomycin yield through streptomyces lincolnensis regulation gene combination modification - Google Patents
Method for improving lincomycin yield through streptomyces lincolnensis regulation gene combination modification Download PDFInfo
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Abstract
The invention discloses a method for improving lincomycin yield through combined modification of streptomyces lincolnensis regulatory genes, which is characterized in that Lrp family transcriptional regulatory genes are combined and knocked out in streptomyces lincolnensisSLCG_4846And TetR family transcriptional regulatory genesSLCG_2919And (4) obtaining the product. Meanwhile, the invention also discloses a method for improving the yield of lincomycin by the combined transformation of streptomyces lincomosus regulatory genes. The method sequentially carries out traceless knockout on a plurality of genes by homologous recombination technology, and resistance genes are not introduced in the process, so that the fermentation cost is reduced, and the genetic stability is also ensured. Meanwhile, the growth of thalli is not influenced in the process, and most importantly, multiple knockout experiments can be continuously carried out in the same strain. The invention can greatly improve the lincomycin yield and can improve the lincomycin for industrial productionThe yield of the mycin provides new technical support.
Description
Technical Field
The invention relates to the technical field of genetic engineering, in particular to a method for improving lincomycin yield through streptomyces lincomosus regulation gene combination modification.
Background
Antibiotics are a class of secondary metabolites that inhibit the growth of pathogenic bacteria, more than half of which are streptomyces. The streptomyces lincolnensis of the invention belongs to one of streptomyces, the produced antibiotic is lincomycin, and the lincomycin is mainly used for treating infection caused by gram-positive bacteria clinically, and the derivative of the lincomycin has better effect on treating bacterial infection, especially anaerobic bacterial infection.
The genetic modification of streptomyces lincolnensis is uninterrupted, and the traditional mutagenesis method is time-consuming, has high randomness and is not suitable for further genetic modification. Since the twenty-first century, novel and efficient genetic engineering technologies such as large-fragment homologous recombination, Cre/loxP and CRIPSR/Cas 9 bring opportunities for genetic improvement of streptomyces lincolnensis to improve the yield of lincomycin biosynthesis.
Lincomycin is formed by condensation of propylproline (PPL) and Lincosamide (LSM) and then modified, and is acted by various regulatory factors in the process. In recent years, a variety of regulatory factors, such as Lrp, TetR, BldD, LmbU, BldA and AdpA, have been found to regulate lincomycin biosynthesis. However, compared with other antibiotics, the research on the biosynthesis and control of lincomycin is relatively limited, and the directed modification of streptomyces lincomycin to obtain high-yield strains is not facilitated. The invention aims to obtain a lincomycin high-yield strain by knocking out two regulatory genes in a gene engineering way in a combined way, is used for producing lincomycin or intermediate products, and lays a foundation for modifying a plurality of regulatory genes.
The Lrp (Leucine-responsive regulatory protein) family is a transcription regulatory factor widely existing in bacteria and archaea, and participates in a plurality of important physiological processes such as microbial hair generation, heavy metal transport, polypeptide transportation, energy metabolism and the like. Recently, various Lrp/AsnC family transcriptional regulators of actinomycetes are reported to be involved in antibiotic production and morphological differentiation, such as BkdR, SCO2140, SACE _ Lrp, SCO3361, SACE _5717, SLCG _ Lrp and the like, and the importance of Lrp family regulatory genes in actinomycetes antibiotic biosynthesis is suggested.
The TetR Family transcription regulating factors (TFRs) play an important role in regulating physiological processes such as biosynthesis of antibiotics, morphological differentiation of thalli, drug efflux, primary metabolism, quorum sensing, coping with osmotic stress and the like. In recent years, various TFRs involved in antibiotic production and morphological differentiation of Streptomyces have been reported, such as SAV _576, SAV _3619, SCO _1712, AtrA, SLCG _2919, etc., suggesting the importance of TetR family regulatory genes in Streptomyces secondary metabolism and antibiotic biosynthesis.
Disclosure of Invention
The invention aims to make up for the defects of the prior art, and provides a method for improving the yield of lincomycin by modifying streptomyces lincomycin regulatory gene combinations, so that the yield of the lincomycin is further improved, and a lincomycin high-yield strain is obtained. The genome of streptomyces lincolensis contains a plurality of genes for coding Lrp family transcription regulating factors, and the genes are subjected to knockout experiments to find that: after the SLCG-4846 gene is deleted, the lincomycin yield of the strain is improved by 23 percent compared with that of the original strain. The SLCG-4846 gene is supplemented back in the deletion mutant strain, the lincomycin yield is restored to the level of the original strain, and the SLCG-4846 negatively regulates the biosynthesis of the lincomycin. And then SLCG-4846 is knocked out in an industrial strain LA219X, so that the yield of the mutant strain is remarkably improved, and the amplification reaches 11.5%.
The early laboratory discovers that the transcription regulatory factor SLCG-2919 of the TetR family has negative regulation effect on the biosynthesis of lincomycin.
In order to further improve the yield of lincomycin, the invention carries out combined transformation on two regulatory factors, namely SLCG-4846 and SLCG-2919, and obtains a double knock-out strain LA219X delta 4846-2919.
The invention is realized by the following technical scheme:
a method for improving the yield of lincomycin through the modification of streptomyces lincomycin regulation gene combinations is characterized in that the gene combinations of Lrp family transcription regulation factors and TetR family transcription regulation factors in streptomyces lincomycin are subjected to traceless knockout through homologous recombination, strains are obtained after knockout, and the obtained strains are used for producing lincomycin through fermentation.
Resistance genes are not introduced in the homologous recombination traceless knockout process, and multiple knockout experiments are continuously carried out in the same strain.
The gene for coding the Lrp family transcription regulating factor is SLCG-4846 gene, the gene for the TetR family transcription regulating factor is SLCG-2919 gene, and SLCG-4846 and SLCG-2919 gene products can negatively regulate lincomycin biosynthesis.
The construction method specifically comprises the following steps:
(1) amplifying an SLCG-4846 upstream fragment by taking a streptomyces linkensis high-yield strain LCGL genome as a template and 4846-P1 and 4846-P2 as primers; amplifying a SLCG _4846 downstream fragment by using 4846-P3 and 4846-P4 as primers;
(2) connecting the upstream and downstream fragments of SLCG-4846 to a pKC1139 vector in a manner of enzyme digestion and connection to construct a pKC 1139-delta 4846 vector;
(3) the pKC 1139-delta 4846 vector is transformed into streptomyces lincolensis LCGL, and after screening, the SLCG-4846 deletion mutant delta SLCGL-4846 is obtained.
The application of the deletion mutant strain in improving the yield of lincomycin at the fermentation level.
SLCG-4846 is transformed in an industrial strain LA219X by the following method:
(1) amplifying an SLCG _4846 upstream fragment by taking a streptomyces lincolnensis high-yield strain LA219X genome as a template and 4846-P1 and 4846-P2 as primers; amplifying a SLCG _4846 downstream fragment by using 4846-P3 and 4846-P4 as primers;
(2) connecting the upstream and downstream fragments of SLCG-4846 to a pKC1139 vector in a manner of enzyme digestion and connection to construct a pKC 1139-delta 4846 vector;
(3) the pKC 1139-delta 4846 vector is transformed into Streptomyces lincolnensis LA219X, and after screening, the SLCG _4846 deletion mutant LA219X delta 4846 is obtained.
The application of the industrial mutant strain in improving the yield of lincomycin at the fermentation level.
A combined deletion mutant strain is constructed on the basis of the deletion mutant strain LA219X delta 4846 by the following method:
(1) amplifying an SLCG _2919 upstream fragment by taking a streptomyces lincolnensis high-producing strain LA219X genome as a template and 2919-P1 and 2919-P2 as primers; amplifying SLCG _2919 downstream fragments by using 2919-P3 and 2919-P4 as primers;
(2) connecting the upstream and downstream fragments of SLCG-2919 to a pKC1139 vector in a mode of enzyme digestion and connection to construct a pKC 1139-delta 2919 vector;
(3) the pKC 1139-delta 2919 vector is transformed into an industrial deletion mutant strain LA219X delta 4846, and after screening, a combined deletion mutant strain LA219X delta 4846-2919 is obtained.
The application of the combined deletion mutant strain in improving the yield of lincomycin at the fermentation level.
The invention has the advantages that:
in the research of the invention, a lincomycin biosynthesis negative regulator SLCG-4846 is screened, and a lincomycin high-yield strain can be obtained by deleting SLCG-4846 genes on a streptomyces lincomycin chromosome through a genetic engineering approach.
SLCG _2919 negatively regulates lincomycin biosynthesis. SLCG-2919 is knocked out in streptomyces lincomycin, and the yield of lincomycin is obviously improved. In order to seek for more high-yield streptomyces lincolnensis, the invention carries out combined transformation on two regulatory genes, namely SLCG-4846 and SLCG-2919, obtains the streptomyces lincolnensis LA219X delta 4846-2919, further improves the lincomycin yield, and provides technical support for improving the lincomycin fermentation yield in industrial production. In addition, the combined knockout of two regulatory genes in Streptomyces lincolensis is the first case.
The construction method of the combined modified strain is simple, and a resistance gene is not introduced in the knockout process, so that the fermentation cost is reduced, and the genetic stability is also ensured. Meanwhile, the knockout does not affect the growth of the thalli. Most importantly, multiple knockout experiments can be continuously carried out in the same strain, and a foundation is laid for further modification of high-yield strains.
Drawings
FIG. 1 shows the positional information of SLCG-4846 gene and neighboring genes on a chromosome.
FIG. 2 is a schematic diagram of the construction of the Δ SLCGL _4846 mutant and the PCR identification of deletion mutants, wherein:
(A) the construction of the Δ SLCGL _4846 mutant is shown schematically;
(B) PCR identification of Δ SLCGL _4846 mutant.
FIG. 3 shows the construction of SLCG-4846 gene complementation strain, PCR identification of Δ SLCGL-4846/pIB 139-4846 complementation strain and Δ SLCGL-4846/pIB 139 complementation empty strain: the PCR product was the apr resistance gene (776 bp).
FIG. 4 shows the effect of SLCG-4846 gene on the morphological differentiation of strain and the determination of biomass of the mutant strain Δ SLCGL-4846, in which:
(A) measuring the biomass of the delta SLCGL-4846 mutant strain and the mycelium of the starting strain LCGL strain;
(B) spore growth of the Δ SLCGL _4846 mutant and the starting strain LCGL strain.
FIG. 5 is HPLC analysis of original strain LCGL, deletion mutant strain Δ SLCGL _4846, deletion anaplerotic strain and anaplerotic no-load control strain lincomycin.
FIG. 6 shows the construction of LA 219X. delta. 4846-2919 mutant and the PCR identification of deletion mutant:
(A) schematic diagram of LA 219X. delta. 4846-2919 mutant construction;
(B) PCR identification of LA 219X. DELTA.4846-2919 mutant.
FIG. 7 shows the effect of SLCG-4846 and SLCG-2919 genes on the morphological differentiation of strains and the determination of biomass of LA 219X. DELTA. 4846 mutant strain, in which:
(A) biomass measurement of mycelium of LA 219X. DELTA.4846-2919 mutant strain and LA219X starting strain;
(B) spore outgrowth of the LA 219X. DELTA.4846-2919 mutant strain and the starting strain LA219X strain.
FIG. 8 shows the analysis of the lincomycin production of the starting strain LA219X, the single-knock mutant LA 219X. delta. 4846 and the double-knock mutant LA 219X. delta. 4846-2919.
Detailed Description
The technical scheme of the invention is further explained by combining the specific examples as follows:
the strains and plasmids used in the examples are shown in Table 1, and the sequences of the primers synthesized are shown in Table 2. Coli were cultured on liquid LB medium at 37 ℃ or on solid LB plates supplemented with 1.25% agar. The lincomycin producing strain streptomyces lincolnensis and its engineering strain are cultured in Tryptone Soy Broth (TSBY) medium at 30 ℃ or on MGM plates containing 2.2% agar.
The materials used in the examples were PEG3350, lysozyme, TES, casamino acid, thiostrepton, apramycin from Sigma. TSB, yeast extract, peptone were purchased from Oxoid. Glycine, agar powder, sodium chloride and other biological reagents were purchased from reagent companies. General procedures for E.coli and S.lincolnensis were performed according to standard protocols. The synthesis of primers and DNA sequencing were performed by Biotechnology engineering (Shanghai) Inc.
Table 1 strains and plasmids used in the study
TABLE 2 primers used in this study
Example 1
Construction of deletion mutant of SLCG-4846 Gene:
as shown in FIGS. 1 and 2, in order to knock out the SLCG-4846 gene in Streptomyces lincolnensis, homologous fragments of about 1.8kb at the upstream and downstream of the SLCG-4846 gene were PCR-amplified using 4846-P1/4846-P2 and 4846-P3/4846-P4 as primers and the LCGL genome of Streptomyces lincolnensis as a template, respectively. The two 4846-U and 4846-D upstream and downstream fragments were ligated to pKC1139 vector at the same time to complete the construction of plasmid pKC 1139. delta. 4846, as shown in A in FIG. 2. A protoplast transformation technology is utilized to transform the pKC1139 delta 4846 plasmid into a streptomyces lincolnensis protoplast, and a positive mutant strain is screened according to the apramycin resistance, so that a gene engineering strain knocked out by the SLCG _4846 gene is obtained. The primers 4846-P5 and 4846-P6 were used as primers for identification, plasmid pKC 1139. DELTA. 4846 was used as a positive template, LCGL genome was used as a negative template for PCR identification, and the positive deletion mutant was named as. DELTA.SLCGL-4846 (shown in FIG. 2 as B).
Example 2
Construction of SLCG-4846 Gene-recovering Strain:
the SLCG-4846 gene is amplified by using designed primers 4846-P7 and 4846-P8, and is recovered by electrophoresis, the recovered SLCG-4846 gene fragment and pIB139 are subjected to double enzyme digestion by using NdeI and XbaI endonucleases respectively and are recovered, the SLCG-4846 gene fragment is connected to the pIB139 by using T4 DNA ligase, and the plasmid pIB139-4846 is successfully obtained. pIB139-4846 and pIB139 were then introduced into Δ SLCGL _4846 protoplasts by the PEG-mediated transformation of protoplasts. Through the primary screening of apramycin, PCR identification is carried out by taking an apramycin resistance gene (apr, 776bp) as an object, and the obtained revertants are named as delta SLCGL _4846/pIB139-4846 and a anaplerotic empty-load strain delta SLCGL _4846/pIB139 (see figure 3).
Example 3
And (3) detecting the biomass of the streptomyces lincolensis mycelium:
respectively inoculating the Delta SLCGL-4846 mutant strain and LCGL in liquid TSBY with the same inoculation amount, carrying out shake culture at 30 ℃ for 48 hours, then transferring to 50mLYMG culture medium, carrying out shake culture at 30 ℃ and 240rpm for 7d, setting different time periods for sampling, washing with absolute ethyl alcohol, drying and weighing the dry weight of the thallus, repeatedly sampling twice each time, obtaining an average value, and drawing a thallus biomass curve according to experimental data after the measurement is finished, wherein as shown in B in figure 4, the deletion of SLCG-4846 gene does not obviously affect the biomass of the thallus.
Example 4
And (3) observing the spore morphology of the streptomyces lincolensis:
marking on an industrial culture medium, respectively coating the spore glycerol bacterial liquid of LCGL and delta SLCGL-4846 on the industrial culture medium with the same inoculation amount, airing in a super clean bench, and then placing in a constant temperature incubator at 30 ℃ for inverted growth. Spore growth was observed and recorded every 24h, and as shown in a in fig. 4, deletion of SLCG _4846 did not affect spore morphology of the cells.
Example 5
And (3) HPLC detection of the fermentation product of the streptomyces lincolensis:
the cells were cultivated with LCGL,. DELTA.SLCGL-4846,. DELTA.SLCGL-4846/pIB 139 and. DELTA.SLCGL-4846/pIB 139-4846Coating glycerol bacterial liquid on slant culture medium, culturing for 7d, digging 1cm2Inoculating to a seed culture medium, carrying out shake culture at 30 ℃ for 48 hours, transferring to a fermentation culture medium, carrying out shake culture at 30 ℃ for 7 days, and centrifuging 2ml of bacterial liquid at 12000rpm for 10 min; then 200ul of supernatant is taken and added with 800ul of absolute ethyl alcohol to be mixed evenly, and centrifugation is carried out for 10 minutes at 12000 rpm; and finally, injecting the supernatant into a detection bottle through an organic filter membrane for yield detection, wherein as shown in fig. 5, compared with the original strain LCGL, the yield of the delta SLCGL _4846 mutant lincomycin A is improved by 23%, and after SLCG _4846 is supplemented in the delta SLCGL _4846, the yield of the mutant lincomycin A is restored to the level of the original strain, which indicates that SLCG _4846 plays a negative regulation role in lincomycin biosynthesis. Then, fermentation experiments are also carried out on the industrial strain LA219X, the single knock-out strain LA219X delta 4846 and the double knock-out strain LA219X delta 4846-2919, and after HPLC detection, fermentation products are found to be: as shown in FIG. 8, the yield of the single knock-out strain LA 219X. delta. 4846 was 2.80g/L, which is 11.5% higher than that of the original strain, and the yield of the double knock-out mutant LA 219X. delta. 4846-E2919 was 12.1% higher than that of the single knock-out strain, which is 25.1% higher than that of the original strain. The construction process of the double knock-out mutant is described in example 1, and the biomass detection and spore morphology observation are described in examples 3 and 4, which are specifically shown in FIGS. 6 and 7.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents and improvements made within the spirit and principle of the present invention are intended to be included within the scope of the present invention.
Sequence listing
<110> university of Anhui
<120> method for improving lincomycin yield through streptomyces lincomosus regulation gene combination modification
<160> 1
<170> SIPOSequenceListing 1.0
<210> 1
<211> 407
<212> DNA
<213> Streptomyces lincolnensis
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tagaagcgac gtggacggcc tggaaaagaa ttcggtcgat accggcttcc gcggcagctc 120
atccaggccc tgatacggga gacgcccttg gtgaaacata tgatggacgc ggtggacagg 180
caaaatctag actatgcctc ttcgggcagc tgcaatacga atggcgaaaa gctggcggat 240
gcaggaagat caaaaagctt ggcaagccgg tggacacgct aaatctagac tccgacacga 300
cctcgtacaa aagatatctt cgggctgttg gaggcgggaa agaattccgt acagccggtg 360
caggcccatg gctgagatcg ggctgcgtta ctcggtaacg ctctccg 407
Claims (3)
1. A method for improving the yield of lincomycin by the combined transformation of streptomyces lincomycin regulatory genes is characterized in that: the gene combination of the Lrp family transcription regulating factor and the TetR family transcription regulating factor in the streptomyces lincomosus is subjected to traceless knockout by homologous recombination, a strain is obtained after knockout, and the obtained strain is used for producing lincomycin by fermentation.
2. The method for improving lincomycin production through streptomyces lincomycin regulatory gene combination modification according to claim 1, wherein the method comprises the following steps: resistance genes are not introduced in the homologous recombination traceless knockout process, and multiple knockout experiments are continuously carried out in the same strain.
3. The method for improving lincomycin production through streptomyces lincomycin regulatory gene combination modification according to claim 1, wherein the method comprises the following steps: the gene for coding the Lrp family transcription regulating factor isSLCG_4846Genes, the genes of the TetR family transcriptional regulators areSLCG_2919A gene, andSLCG_4846andSLCG_2919the gene products can negatively regulate the biosynthesis of the lincomycin.
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