EP3435770A1 - Production of milk with low lactose content - Google Patents

Production of milk with low lactose content

Info

Publication number
EP3435770A1
EP3435770A1 EP17714717.0A EP17714717A EP3435770A1 EP 3435770 A1 EP3435770 A1 EP 3435770A1 EP 17714717 A EP17714717 A EP 17714717A EP 3435770 A1 EP3435770 A1 EP 3435770A1
Authority
EP
European Patent Office
Prior art keywords
milk
seq
lactose
lactase activity
sequence
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP17714717.0A
Other languages
German (de)
French (fr)
Inventor
Petrus Jacobus Theodorus Dekker
Cornelis Marinus Muijlwijk
Marten Aalt PAASMAN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DSM IP Assets BV
Original Assignee
DSM IP Assets BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by DSM IP Assets BV filed Critical DSM IP Assets BV
Publication of EP3435770A1 publication Critical patent/EP3435770A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y302/00Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01108Lactase (3.2.1.108)
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; PREPARATION THEREOF
    • A23C9/00Milk preparations; Milk powder or milk powder preparations
    • A23C9/12Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/1203Addition of, or treatment with, enzymes or microorganisms other than lactobacteriaceae
    • A23C9/1206Lactose hydrolysing enzymes, e.g. lactase, beta-galactosidase
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/24Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; PREPARATION THEREOF
    • A23C2220/00Biochemical treatment
    • A23C2220/10Enzymatic treatment

Definitions

  • the invention relates to a milk obtainable by a process in which a milk comprising lactose is treated with an enzyme composition comprising lactase activity.
  • the invention also relates to the process itself and to use of an enzyme composition comprising lactase activity in the production of a milk with a low lactose content.
  • Lactose intolerance is perhaps the best-known food sensitivity in the United States and other parts of the world. It is estimated that about 70% of the world's population has a genetically controlled limited ability to digest lactose. Accordingly, there is a growing demand for dairy food products that contain no or only low levels of lactose.
  • Lactase is used commercially to break down lactose in milk to produce dairy products which are suitable for people with lactose intolerance and/or have a sweeter taste. Because glucose and galactose are sweeter than lactose, lactase produces a more pleasant taste. Lactase is also used in the manufacture of ice cream. Lactose crystallizes at the low temperatures of ice cream, whereas glucose and galactose stay liquid and contribute to a smoother texture. Lactase is also used in the conversion of whey into syrup and for the production of condensed milk.
  • the present invention relates to a milk, to a process for production of such a milk and to the use of a lactase composition in a process for the production of a milk having low lactose.
  • the milk may have a low level of lactose (in view of the use of the lactase, i.e. low lactose lactase-treated milk).
  • a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
  • the invention also provides:
  • a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; a process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
  • lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; a process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
  • lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; a process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
  • lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; a process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
  • lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; and use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
  • SEQ ID NOs: 1 and 2 set out the polypeptide sequences of lactase enzymes from Bifidobacterium bifidum.
  • SEQ ID NO: 1 may also be defined with reference to SEQ ID NO: 2 in WO01/90317.
  • SEQ ID NO: 2 may also be defined with reference to the Bbg3 sequence described in Goulas T.K., Goulas A.K., Tzortzis G., Gibson G.R., Appl. Microbiol. Biotechnol. 76(6), 1365 and 1372 (2007).
  • SEQ ID NO: 3 a C-terminal truncation variant, may also be defined with reference to SEQ ID NO: 2 as described in WO2009/071539.
  • SEQ ID NO: 4 another C-terminal truncation variant, may also be defined with reference to SEQ ID NO: 2 as described in WO2014/184189.
  • the articles “a” and “an” are used herein to refer to one or to more than one (i.e. to one or at least one) of the grammatical object of the article.
  • an element may mean one element or more than one element.
  • the invention provides a milk comprising about 50 mg/L or less lactose. The inventors of the present patent application were surprised that a (lactase-treated) milk with such low levels of lactose could be produced/obtained, the invention thus provides a low lactose, lactase-treated milk.
  • the invention concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • the invention also concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • At least a part of the lactase activity in the enzyme composition may be provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
  • Reference to a truncated version refers to a C-terminal truncated version.
  • At least a part of the lactase activity in the enzyme composition may be provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ I D NO: 2 or SEQ ID NO: 3 or SEQ ID NO: 4 or a sequence having at least about 60% sequence identity to any thereto
  • at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
  • a substance e.g., a nucleic acid molecule or polypeptide
  • derived from a microorganism preferably means that the substance is native to that microorganism or is a variant based on a substance native to the microorganism (for example a truncated version of a polypeptide derived from the microorganism and/or a version which contains one or more substitutions as compared to a polypeptide derived from the microorganism).
  • polypeptide set out in SEQ ID NO: 1 or SEQ ID NO: 2 of the invention is a full-length wild-type sequence of a lactase from Bifidobacterium bifidum.
  • a polypeptide having lactase activity suitable for use in the invention may comprise an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to SEQ ID NO: 1 or SEQ ID NO: 2.
  • SEQ ID NO: 1 and 2 both comprise a signal sequence which is positioned at amino acids 1 to 32 for both of them.
  • a polypeptide having lactase activity for use in the invention preferably comprises:
  • amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 33 to 1752 of SEQ ID NO: 1 .
  • amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 33 to 1935 of SEQ ID NO: 2.
  • a truncated version of the polypeptide of SEQ ID NO: 1 or SEQ ID NO: 2, or more preferably a truncated version of amino acids 33 to 1752 of SEQ ID NO: 1 or a truncated version of amino acids 33 to 1935 of SEQ ID NO:2, may be used or a polypeptide comprising an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to such a truncated version of SEQ ID NO: 1 or SEQ ID NO: 2 or more preferred to a truncated version of amino acids 33 to 1752 of SEQ ID NO:
  • polypeptide having lactase activity suitable for use in the invention is the Bbg3 polypeptide described in Goulas T.K., Goulas A.K., Tzortzis G., Gibson G.R., Appl. Microbiol. Biotechnol. 76(6), 1365 and 1372 (2007).
  • Suitable truncated versions of the polypeptide of SEQ ID NO: 1 or SEQ ID NO: 2 include SEQ ID NO: 2 in WO2009/071539 (herein SEQ ID NO: 3) and SEQ ID NOs: 1 or 2 in WO2014/184189 (SEQ ID NO: 2 of WO2014/184189 is SEQ ID NO: 4 in this patent application).
  • the invention provides a milk or a process according to the invention in which SEQ ID NO: 3 or 4 is used or a polypeptide comprising an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to SEQ ID NO: 3 or SEQ ID NO: 4.
  • SEQ ID NO: 3 and 4 both comprise a signal sequence which is positioned at amino acids 1 to 27 for both of them.
  • a polypeptide having lactase activity for use in the invention preferably comprises:
  • amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 28 to 1341 of SEQ I D NO: 3, more preferably amino acids 28-1331 of SEQ ID NO: 3 (as amino acids 1332-1341 comprise a purification tag which is preferably removed)
  • amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 28 to 1331 of SEQ ID NO: 4.
  • the invention concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • the invention also concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
  • lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 , 2, 3 or 4 or a sequence having at least 60% sequence identity to SEQ ID NO: 1 , 2, 3 or 4.
  • At least part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in amino acids 33 to 1752 of SEQ ID NO: 1 , amino acids 33 to 1935 of SEQ I D NO: 2, amino acids 28 to 1331 of SEQ ID NO:3 or amino acids 28 to 1331 of SEQ ID NO: 4 or a sequence having at least 60% sequence identity to any thereto.
  • a low temperature batch process is one which is typically carried out a temperature of from about 5°C to about 10°C, for example at about 6°C to about 9°C.
  • the enzyme composition comprising lactase activity may be used so that from about 2000 to about 5000 NLU/L lactase activity is provided. More preferably, the skilled person determines the suitable amount of enzyme based on the specific enzyme characteristics. The skilled person is very well capable of determining the suitable amount of enzyme needed to achieve the desired degree of lactose hydrolysis. The enzyme activity may also be expressed in a different unit, for example in LAU.
  • the used incubation time depends on the amount of NLU/L milk and is typically in the range of 20 to 48 hours.
  • the low temperature batch process is performed at from about 5°C to about 10°C and incubation is performed from about 20 to about 48 hours.
  • An aseptic process is one which is typically carried out at ambient temperature, for example a temperature of at least about 20°C, for example at least about 25°C.
  • the enzyme composition comprising lactase activity may be used so that from about 200 to about 500 NLU/L lactase activity is provided.
  • An aseptic process may be the FlexDosTM or Aldose systems.
  • An aseptic process is a process in which milk is first pasteurized or sterilized and cooled to ambient temperature, at which time sterile filtered lactase is added and the product sterile packed. The lactase is allowed to react with lactose in the milk over several days.
  • An example of a resulting milk is low lactose UHT milk.
  • the invention provides a milk obtainable by the process of the invention.
  • milk is intended to encompass milks from mammals and plant sources or mixtures thereof.
  • the milk is from a mammal source.
  • Mammals sources of milk include, but are not limited to cow, sheep, goat, buffalo, camel, llama, mare and deer.
  • the milk is from a mammal selected from the group consisting of cow, sheep, goat, buffalo, camel, llama, mare and deer, and combinations thereof.
  • Plant sources of milk include, but are not limited to, milk extracted from soy bean, pea, peanut, barley, rice, oat, quinoa, almond, cashew, coconut, hazelnut, hemp, sesame seed and sunflower seed. Soy bean milk is preferred.
  • milk refers to not only whole milk, but also skim milk or any liquid component derived thereof.
  • low lactose milk refers to a milk which comprises about 50mg/L or less lactose, about 40mg/L or less lactose, about 30mg/L or less lactose, about 20mg/L or less lactose or about 10mg/L or less lactose. Such concentrations may be reached in about 48 hours or less, about 32 hours or less or about 24 hours or less (when a milk is treated as described herein).
  • the milk could be a pasteurized milk, a UHT-milk or milk reconstituted from all or part of its original constituents with or without intermediate processing steps such as protein hydrolysis.
  • Treatment with an enzyme composition comprising lactase activity may be done prior to and after the heat-treatment of the milk.
  • the lactase treatment may be done by adding the enzyme to the milk.
  • the invention also provides:
  • the enzyme composition comprising lactase activity may be as described herein.
  • milk with a low lactose content refers to a milk which comprises about 50mg/L or less lactose, about 40mg/L or less lactose, about 30mg/L or less lactose, about 20mg/L or less lactose or about 10mg/L or less lactose.
  • sequence homology or “sequence identity” or “homology” or “identity” are used interchangeably herein.
  • sequences are aligned for optimal comparison purposes.
  • gaps may be introduced in any of the two sequences that are compared.
  • alignment can be carried out over the full length of the sequences being compared.
  • the alignment may be carried out over a shorter length, for example over about 20, about 50, about 100 or more nucleic acids/based or amino acids.
  • sequence identity is the percentage of identical matches between the two sequences over the reported aligned region.
  • a comparison of sequences and determination of percentage of sequence identity between two sequences can be accomplished using a mathematical algorithm.
  • the skilled person will be aware of the fact that several different computer programs are available to align two sequences and determine the identity between two sequences (Kruskal, J. B. (1983) An overview of sequence comparison In D. Sankoff and J. B. Kruskal, (ed.), Time warps, string edits and macromolecules: the theory and practice of sequence comparison, pp. 1 -44 Addison Wesley).
  • the percent sequence identity between two amino acid sequences or between two nucleotide sequences may be determined using the Needleman and Wunsch algorithm for the alignment of two sequences. (Needleman, S. B. and Wunsch, C. D. (1970) J. Mol. Biol.
  • the percentage of sequence identity between a query sequence and a sequence of the invention is calculated as follows: Number of corresponding positions in the alignment showing an identical amino acid or identical nucleotide in both sequences divided by the total length of the alignment after subtraction of the total number of gaps in the alignment.
  • the identity defined as herein can be obtained from NEEDLE by using the NOBRIEF option and is labeled in the output of the program as "longest-identity".
  • nucleic acid and protein sequences of the present invention can further be used as a "query sequence" to perform a search against public databases to, for example, identify other family members or related sequences.
  • search can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. (1990) J. Mol. Biol. 215:403—10.
  • Gapped BLAST can be utilized as described in Altschul et al., (1997) Nucleic Acids Res. 25(17): 3389-3402.
  • the default parameters of the respective programs e.g., XBLAST and NBLAST
  • Lactase enzymes were expressed in Bacillus subtilis for comparison with Maxilact LGI (DSM Food Specialties, Delft, NL).
  • Lad 6 is described in WO2009/071538 (SEQ ID NO: 2; herein SEQ ID NO: 3) and Iac19 (herein SEQ ID NO: 2) is described as Bbg3 in Goulas T.K., Goulas A.K., Tzortzis G., Gibson G.R., Appl. Microbiol. Biotechnol. 76(6), 1365 and 1372 (2007).
  • Standard genetic techniques such as overexpression of enzymes in the host cells, genetic modification of host cells, or hybridisation techniques, are known methods in the art, such as described in Sambrook and Russel (2001 ) "Molecular Cloning: A Laboratory Manual (3 rd edition), Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, or F. Ausubel et al, eds., "Current protocols in molecular biology", Green Publishing and Wiley Interscience, New York (1987). Methods for transformation, genetic modification etc of fungal host cells are known from e.g.
  • Enzymes were isolated from the fermentation broth of Bacillus subtilis strains and purified using standard centrifugation and filtration techniques.
  • Example 1 application of the lactase enzymes in the milk pre-sterilization process (6°C)
  • Substrate "Halfvolle melk from Jumbo supermarket”. For each enzyme 2 vials each containing 18.4 ml of semi-skimmed pasteurized and homogenized milk was equilibrated at 6°C before start of the experiment. Lactase was dosed based on the amount of specific protein at 20 mg/l milk in duplicate and incubation is continued at 6°C.
  • the different Bifidobacterium lactases were tested for activity in pasteurized milk by incubation at 6°C and taking samples at various time points, as described above.
  • This method represents the batch process (also called pre-sterilization process).
  • the different Bifidobacterium lactases were dosed in UHT milk and incubated at 25°C, representing the aseptic process (also called post-sterilization process). Dosage of all lactases was based on the protein giving however the most fair comparison between the Bifidobacterium lactases and Maxilact.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Dairy Products (AREA)
  • Enzymes And Modification Thereof (AREA)

Abstract

The invention provides a milk obtainable by a process which comprises: a) providing a milk comprising lactose; and b) treating said milk in a low temperature batch process or an aseptic process with an enzyme composition comprising lactase activity, wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ I D NO: 1 OR SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.

Description

PRODUCTION OF MILK WITH LOW LACTOSE CONTENT
Field of the invention
The invention relates to a milk obtainable by a process in which a milk comprising lactose is treated with an enzyme composition comprising lactase activity. The invention also relates to the process itself and to use of an enzyme composition comprising lactase activity in the production of a milk with a low lactose content.
Background to the invention
Lactose intolerance is perhaps the best-known food sensitivity in the United States and other parts of the world. It is estimated that about 70% of the world's population has a genetically controlled limited ability to digest lactose. Accordingly, there is a growing demand for dairy food products that contain no or only low levels of lactose.
Lactase is used commercially to break down lactose in milk to produce dairy products which are suitable for people with lactose intolerance and/or have a sweeter taste. Because glucose and galactose are sweeter than lactose, lactase produces a more pleasant taste. Lactase is also used in the manufacture of ice cream. Lactose crystallizes at the low temperatures of ice cream, whereas glucose and galactose stay liquid and contribute to a smoother texture. Lactase is also used in the conversion of whey into syrup and for the production of condensed milk.
It is desirable to provide new dairy products having low-amounts of lactose and methods for their production.
Summary of the invention
The present invention relates to a milk, to a process for production of such a milk and to the use of a lactase composition in a process for the production of a milk having low lactose. The milk may have a low level of lactose (in view of the use of the lactase, i.e. low lactose lactase-treated milk). According to the invention, there is thus provided a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
The invention also provides:
a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; a process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; a process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
a) providing a milk comprising lactose; and b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; a process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; a process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum; use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto; and use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
Description of the sequence listing
SEQ ID NOs: 1 and 2 set out the polypeptide sequences of lactase enzymes from Bifidobacterium bifidum. SEQ ID NO: 1 may also be defined with reference to SEQ ID NO: 2 in WO01/90317. SEQ ID NO: 2 may also be defined with reference to the Bbg3 sequence described in Goulas T.K., Goulas A.K., Tzortzis G., Gibson G.R., Appl. Microbiol. Biotechnol. 76(6), 1365 and 1372 (2007).
SEQ ID NO: 3, a C-terminal truncation variant, may also be defined with reference to SEQ ID NO: 2 as described in WO2009/071539.
SEQ ID NO: 4, another C-terminal truncation variant, may also be defined with reference to SEQ ID NO: 2 as described in WO2014/184189.
Detailed description of the invention
Throughout the present specification and the accompanying claims, the words "comprise", "include" and "having" and variations such as "comprises", "comprising", "includes" and "including" are to be interpreted inclusively. That is, these words are intended to convey the possible inclusion of other elements or integers not specifically recited, where the context allows.
The articles "a" and "an" are used herein to refer to one or to more than one (i.e. to one or at least one) of the grammatical object of the article. By way of example, "an element" may mean one element or more than one element. The invention provides a milk comprising about 50 mg/L or less lactose. The inventors of the present patent application were surprised that a (lactase-treated) milk with such low levels of lactose could be produced/obtained, the invention thus provides a low lactose, lactase-treated milk.
The invention concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity.
The invention also concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity.
Further provided is a process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity.
In addition is provided a process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
At least a part of the lactase activity in the enzyme composition may be provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto. Reference to a truncated version refers to a C-terminal truncated version.
Alternatively, at least a part of the lactase activity in the enzyme composition may be provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ I D NO: 2 or SEQ ID NO: 3 or SEQ ID NO: 4 or a sequence having at least about 60% sequence identity to any thereto In addition or alternatively, at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum. The term "derived from" also includes the terms "originated from," "obtained from," "obtainable from," "isolated from," and "created from," and generally indicates that one specified material find its origin in another specified material or has features that can be described with reference to the another specified material. As used herein, a substance (e.g., a nucleic acid molecule or polypeptide) "derived from" a microorganism preferably means that the substance is native to that microorganism or is a variant based on a substance native to the microorganism (for example a truncated version of a polypeptide derived from the microorganism and/or a version which contains one or more substitutions as compared to a polypeptide derived from the microorganism).
The polypeptide set out in SEQ ID NO: 1 or SEQ ID NO: 2 of the invention is a full-length wild-type sequence of a lactase from Bifidobacterium bifidum.
A polypeptide having lactase activity suitable for use in the invention may comprise an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to SEQ ID NO: 1 or SEQ ID NO: 2.
SEQ ID NO: 1 and 2 both comprise a signal sequence which is positioned at amino acids 1 to 32 for both of them. As the signal sequence will most likely be cleaved off during production in a host cell, a polypeptide having lactase activity for use in the invention preferably comprises:
an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 33 to 1752 of SEQ ID NO: 1 .
an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 33 to 1935 of SEQ ID NO: 2.
A truncated version of the polypeptide of SEQ ID NO: 1 or SEQ ID NO: 2, or more preferably a truncated version of amino acids 33 to 1752 of SEQ ID NO: 1 or a truncated version of amino acids 33 to 1935 of SEQ ID NO:2, may be used or a polypeptide comprising an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to such a truncated version of SEQ ID NO: 1 or SEQ ID NO: 2 or more preferred to a truncated version of amino acids 33 to 1752 of SEQ ID NO: 1 or amino acids 33 to 1935 of SEQ ID NO:2.
An example of such a polypeptide, i.e. a polypeptide having lactase activity suitable for use in the invention, is the Bbg3 polypeptide described in Goulas T.K., Goulas A.K., Tzortzis G., Gibson G.R., Appl. Microbiol. Biotechnol. 76(6), 1365 and 1372 (2007).
Suitable truncated versions of the polypeptide of SEQ ID NO: 1 or SEQ ID NO: 2 include SEQ ID NO: 2 in WO2009/071539 (herein SEQ ID NO: 3) and SEQ ID NOs: 1 or 2 in WO2014/184189 (SEQ ID NO: 2 of WO2014/184189 is SEQ ID NO: 4 in this patent application).
In a preferred embodiment, the invention provides a milk or a process according to the invention in which SEQ ID NO: 3 or 4 is used or a polypeptide comprising an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to SEQ ID NO: 3 or SEQ ID NO: 4. SEQ ID NO: 3 and 4 both comprise a signal sequence which is positioned at amino acids 1 to 27 for both of them. As the signal sequence will most likely be cleaved off during production in a host cell, a polypeptide having lactase activity for use in the invention preferably comprises:
an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 28 to 1341 of SEQ I D NO: 3, more preferably amino acids 28-1331 of SEQ ID NO: 3 (as amino acids 1332-1341 comprise a purification tag which is preferably removed)
an amino acid sequence having at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about, 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91 %, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98% or at least about 99% sequence identity to amino acids 28 to 1331 of SEQ ID NO: 4.
Preferably, the invention concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity.
The invention also concerns a milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity.
Further provided is a process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
a) providing a milk comprising lactose; and b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity.
In addition is provided a process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 , 2, 3 or 4 or a sequence having at least 60% sequence identity to SEQ ID NO: 1 , 2, 3 or 4.
More preferably, at least part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in amino acids 33 to 1752 of SEQ ID NO: 1 , amino acids 33 to 1935 of SEQ I D NO: 2, amino acids 28 to 1331 of SEQ ID NO:3 or amino acids 28 to 1331 of SEQ ID NO: 4 or a sequence having at least 60% sequence identity to any thereto.
A low temperature batch process is one which is typically carried out a temperature of from about 5°C to about 10°C, for example at about 6°C to about 9°C.
In a batch process, the enzyme composition comprising lactase activity may be used so that from about 2000 to about 5000 NLU/L lactase activity is provided. More preferably, the skilled person determines the suitable amount of enzyme based on the specific enzyme characteristics. The skilled person is very well capable of determining the suitable amount of enzyme needed to achieve the desired degree of lactose hydrolysis. The enzyme activity may also be expressed in a different unit, for example in LAU.
The used incubation time depends on the amount of NLU/L milk and is typically in the range of 20 to 48 hours.
Preferably, the low temperature batch process is performed at from about 5°C to about 10°C and incubation is performed from about 20 to about 48 hours.
An aseptic process is one which is typically carried out at ambient temperature, for example a temperature of at least about 20°C, for example at least about 25°C.
In an aseptic process, the enzyme composition comprising lactase activity may be used so that from about 200 to about 500 NLU/L lactase activity is provided.
An aseptic process may be the FlexDos™ or Aldose systems. An aseptic process is a process in which milk is first pasteurized or sterilized and cooled to ambient temperature, at which time sterile filtered lactase is added and the product sterile packed. The lactase is allowed to react with lactose in the milk over several days. An example of a resulting milk is low lactose UHT milk.
The invention provides a milk obtainable by the process of the invention. The term "milk" is intended to encompass milks from mammals and plant sources or mixtures thereof. Preferably, the milk is from a mammal source. Mammals sources of milk include, but are not limited to cow, sheep, goat, buffalo, camel, llama, mare and deer. In an embodiment, the milk is from a mammal selected from the group consisting of cow, sheep, goat, buffalo, camel, llama, mare and deer, and combinations thereof. Plant sources of milk include, but are not limited to, milk extracted from soy bean, pea, peanut, barley, rice, oat, quinoa, almond, cashew, coconut, hazelnut, hemp, sesame seed and sunflower seed. Soy bean milk is preferred. In addition, the term "milk" refers to not only whole milk, but also skim milk or any liquid component derived thereof.
As described herein, the present invention relates to low lactose milk. The term low lactose milk refers to a milk which comprises about 50mg/L or less lactose, about 40mg/L or less lactose, about 30mg/L or less lactose, about 20mg/L or less lactose or about 10mg/L or less lactose. Such concentrations may be reached in about 48 hours or less, about 32 hours or less or about 24 hours or less (when a milk is treated as described herein).
The milk could be a pasteurized milk, a UHT-milk or milk reconstituted from all or part of its original constituents with or without intermediate processing steps such as protein hydrolysis.
Treatment with an enzyme composition comprising lactase activity may be done prior to and after the heat-treatment of the milk. The lactase treatment may be done by adding the enzyme to the milk.
The invention also provides:
use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity; and use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity.
The enzyme composition comprising lactase activity may be as described herein.
The term "milk with a low lactose content" refers to a milk which comprises about 50mg/L or less lactose, about 40mg/L or less lactose, about 30mg/L or less lactose, about 20mg/L or less lactose or about 10mg/L or less lactose.
The conditions cited above for the low temperature batch process and the aseptic process (such as for example temperature and amount of lactase) are applicable to the use claims as well.
Moreover, also the description of the suitable lactases are applicable to the use claims as well.
The terms "sequence homology" or "sequence identity" or "homology" or "identity" are used interchangeably herein. For the purpose of this invention, it is defined here that in order to determine the percentage of sequence homology or sequence identity of two amino acid sequences or of two nucleic acid sequences, the sequences are aligned for optimal comparison purposes. In order to optimize the alignment between the two sequences gaps may be introduced in any of the two sequences that are compared. Such alignment can be carried out over the full length of the sequences being compared. Alternatively, the alignment may be carried out over a shorter length, for example over about 20, about 50, about 100 or more nucleic acids/based or amino acids. The sequence identity is the percentage of identical matches between the two sequences over the reported aligned region.
A comparison of sequences and determination of percentage of sequence identity between two sequences can be accomplished using a mathematical algorithm. The skilled person will be aware of the fact that several different computer programs are available to align two sequences and determine the identity between two sequences (Kruskal, J. B. (1983) An overview of sequence comparison In D. Sankoff and J. B. Kruskal, (ed.), Time warps, string edits and macromolecules: the theory and practice of sequence comparison, pp. 1 -44 Addison Wesley). The percent sequence identity between two amino acid sequences or between two nucleotide sequences may be determined using the Needleman and Wunsch algorithm for the alignment of two sequences. (Needleman, S. B. and Wunsch, C. D. (1970) J. Mol. Biol. 48, 443-453). Both amino acid sequences and nucleotide sequences can be aligned by the algorithm. The Needleman-Wunsch algorithm has been implemented in the computer program NEEDLE. For the purpose of this invention the NEEDLE program from the EMBOSS package was used (version 2.8.0 or higher, EMBOSS: The European Molecular Biology Open Software Suite (2000) Rice, P. LongdenJ. and BleasbyA Trends in Genetics 16, (6) pp276— 277, http://emboss.bioinformatics.nl/). For protein sequences EBLOSUM62 is used for the substitution matrix. For nucleotide sequence, EDNAFULL is used. The optional parameters used are a gap-open penalty of 10 and a gap extension penalty of 0.5. The skilled person will appreciate that all these different parameters will yield slightly different results but that the overall percentage identity of two sequences is not significantly altered when using different algorithms.
After alignment by the program NEEDLE as described above the percentage of sequence identity between a query sequence and a sequence of the invention is calculated as follows: Number of corresponding positions in the alignment showing an identical amino acid or identical nucleotide in both sequences divided by the total length of the alignment after subtraction of the total number of gaps in the alignment. The identity defined as herein can be obtained from NEEDLE by using the NOBRIEF option and is labeled in the output of the program as "longest-identity".
The nucleic acid and protein sequences of the present invention can further be used as a "query sequence" to perform a search against public databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. (1990) J. Mol. Biol. 215:403—10. BLAST nucleotide searches can be performed with the NBLAST program, score = 100, wordlength = 12 to obtain nucleotide sequences homologous to nucleic acid molecules as described herein. BLAST protein searches can be performed with the XBLAST program, score = 50, wordlength = 3 to obtain amino acid sequences homologous to protein molecules as described herein. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al., (1997) Nucleic Acids Res. 25(17): 3389-3402. When utilizing BLAST and Gapped BLAST programs, the default parameters of the respective programs (e.g., XBLAST and NBLAST) can be used. See the homepage of the National Center for Biotechnology Information at http://www.ncbi.nlm.nih.gov/.
A reference herein to a patent document or other matter which is given as prior art is not to be taken as an admission that that document or matter was known or that the information it contains was part of the common general knowledge as at the priority date of any of the claims.
The disclosure of each reference set forth herein is incorporated herein by reference in its entirety.
The present invention is further illustrated by the following Examples:
EXAMPLES
Lactase enzymes were expressed in Bacillus subtilis for comparison with Maxilact LGI (DSM Food Specialties, Delft, NL). Lad 6 is described in WO2009/071538 (SEQ ID NO: 2; herein SEQ ID NO: 3) and Iac19 (herein SEQ ID NO: 2) is described as Bbg3 in Goulas T.K., Goulas A.K., Tzortzis G., Gibson G.R., Appl. Microbiol. Biotechnol. 76(6), 1365 and 1372 (2007).
Standard genetic techniques, such as overexpression of enzymes in the host cells, genetic modification of host cells, or hybridisation techniques, are known methods in the art, such as described in Sambrook and Russel (2001 ) "Molecular Cloning: A Laboratory Manual (3rd edition), Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, or F. Ausubel et al, eds., "Current protocols in molecular biology", Green Publishing and Wiley Interscience, New York (1987). Methods for transformation, genetic modification etc of fungal host cells are known from e.g. EP-A-0 635 574, WO 98/46772, WO 99/60102 and WO 00/37671 , WO90/14423, EP-A- 0481008, EP-A-0635 574 and US 6,265,186.
Enzymes were isolated from the fermentation broth of Bacillus subtilis strains and purified using standard centrifugation and filtration techniques.
Example 1 : application of the lactase enzymes in the milk pre-sterilization process (6°C)
Substrate: "Halfvolle melk from Jumbo supermarket". For each enzyme 2 vials each containing 18.4 ml of semi-skimmed pasteurized and homogenized milk was equilibrated at 6°C before start of the experiment. Lactase was dosed based on the amount of specific protein at 20 mg/l milk in duplicate and incubation is continued at 6°C.
After exactly 0.5, 2, 6, 24 and 48 h incubation, vials were gently mixed and 1 .8 mL sample was taken from each vial into an Eppendorf cup (all "incubations vials" were kept in the cold room during the complete experiment). This cup was placed in a thermomixer (10 minutes 90°C). Subsequently the cup was cooled down to room temperature and exactly 1 mL was pipetted in MTP-plate and stored frozen until further analysis (NMR for lactose, glucose and galactose analysis). After 48 hours extra samples were taken to be analyzed using HPEAC-PAD to determine low lactose content. Control sample without enzyme addition was included as well.
In Table 1 the dosage of the various lactases in the application experiments is presented.
Table 1 : dosage of the various lactases in the application experiments
The different Bifidobacterium lactases were tested for activity in pasteurized milk by incubation at 6°C and taking samples at various time points, as described above. This method represents the batch process (also called pre-sterilization process).
Dosage of all lactases was based on the protein giving however the most fair comparison between the Bifidobacterium lactases and Maxilact. Since low lactose concentrations are difficult to measure accurately using NMR analysis, we decided to analyze the last time points (48 hr) of these samples using HPAEC-PAD. A detailed description of this method can be found in: Determination fo lactose in lactose-free milk products by high performance anion-exchange
chromatography with pulsed amperometric detection, Pranathi Perati, Brian de Borba and Jeffrey Rohrer, Thermo Fisher Scientific, Sunnyvale, Ca, USA, Application Note 248, pages 1 -8, 2015). With this method very low amounts of lactose can be detected. Table 2 shows a summary of the average amount of lactose in these samples after 48 hr.
These experiments show that there is a clear difference between the milk hydrolyzed with Maxilact and the milk hydrolyzed with the Bifidobacterium lactases.
Table 2: Amount of lactose in milk after 48 hr at 6°C incubated with different lactases
* calculated based on a generally accepted density of 1 .03
Example 2: Application of the enzymes in the milk post-sterilization process (25°C)
Substrate: "Houdbare Halfvolle melk from Jumbo supermarket" = UHT milk
For each enzyme 2 vials each containing 18.4 ml of semi-skimmed UHT milk was equilibrated at 25°C before start of the experiment. Azide was added to the milk to prevent infection during incubation. Lactases were dosed based on the amount of specific protein at 2 mg/l milk in duplicate and incubation was continued at 25°C. Exactly after 0.5, 2, 6, 24 and 48 h vials were gently mixed and 1.8 mL sample is taken from each vial into an Eppendorf cup. This cup was placed in a thermomixer (10 minutes 90°C). Subsequently the cup was cooled down to room temperature and exactly 1 mL was pipetted in MTP-plate and stored frozen until further analysis (NMR for lactose, glucose and galactose analysis). After 48 hours extra samples were taken to be analyzed using HPEAC-PAD to determine low lactose content. Control sample without enzyme addition was included as well.
In Table 3 the dosage of the various lactases in the application experiments is presented.
Table 3: dosage of the various lactases in the application experiments
The different Bifidobacterium lactases were dosed in UHT milk and incubated at 25°C, representing the aseptic process (also called post-sterilization process). Dosage of all lactases was based on the protein giving however the most fair comparison between the Bifidobacterium lactases and Maxilact.
Since low lactose concentrations are difficult to measure accurately using NMR analysis, we decided to analyze the last time points (48 hr) of these samples using HPAEC-PAD. With this method very low amounts of lactose can be detected. Table 4 shows a summary of the average amount of lactose in these samples after 48 hr.
These experiments show that there is a clear difference between the milk hydrolyzed with Maxilact and the milk hydrolyzed with the Bifidobacterium lactases. Table 4: Amount of lactose in milk after 48 hr at 25°C incubated with different lactases
* calculated based on a generally accepted density of 1.03

Claims

1 . A milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
2. A milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2 or SEQ ID NO: 3 or SEQ ID NO: 4 or a sequence having at least about 60% sequence identity to any thereto.
3. A milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
4. A milk according to claim 1 or 2 or 3, wherein the process is carried out at a temperature of from about 5°C to about 10°C.
5. A milk according to any one of claims 1 to 4, wherein the process is carried out for a time of 20 to 48 hours.
6. A process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
7. A process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2 or SEQ ID NO: 3 or SEQ ID NO: 4 or a sequence having at least about 60% sequence identity to any thereto.
8. A process for the production of a milk comprising about 50 mg/L or less lactose, which process comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
9. A process according to any one of claims 6 to 8, wherein the process is carried out at a temperature of from about 5°C to about 10°C.
10. A process according to any one of claims 6 to 9, wherein the process is carried out for a time of 20 to 48 hours.
1 1 . A milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
12. A milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2 or SEQ ID NO: 3 or SEQ ID NO:4 or a sequence having at least about 60% sequence identity to any thereto.
13. A milk comprising about 50 mg/L or less lactose obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
14. A milk according to claim 1 1 or 13, wherein the process is carried out at a temperature of at least about 20°C.
15. A process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
16. A process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2 or SEQ ID NO: 3 or SEQ ID NO: 4 or a sequence having at least about 60% sequence identity to any thereto.
17. A process for the production of a milk comprising about 50 mg/L or less lactose which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
18. A process according to any one of claims 15 to 17, wherein the process is carried out at a temperature of at least about 20°C.
19. Use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
20. Use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2 or SEQ ID NO: 3 or SEQ ID NO: 4 or a sequence having at least about 60% sequence identity to any thereto.
21 . Use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in a low temperature batch process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum
22. Use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2, a truncated version of either thereof or a sequence having at least about 60% sequence identity to any thereto.
23. Use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having an amino acid sequence which comprises the sequence set out in SEQ ID NO: 1 or SEQ ID NO: 2 or SEQ ID NO: 3 or SEQ ID NO: 4 or a sequence having at least about 60% sequence identity to any thereto.
24. Use of an enzyme having lactase activity in the production of milk with a low lactose content, which milk is obtainable by a process which comprises:
a) providing a milk comprising lactose; and
b) treating said milk in an aseptic process with an enzyme composition comprising lactase activity,
wherein at least a part of the lactase activity is provided by a polypeptide having lactase activity which is derived from Bifidobacterium bifidum.
EP17714717.0A 2016-03-31 2017-03-30 Production of milk with low lactose content Withdrawn EP3435770A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662316460P 2016-03-31 2016-03-31
PCT/EP2017/057488 WO2017167847A1 (en) 2016-03-31 2017-03-30 Production of milk with low lactose content

Publications (1)

Publication Number Publication Date
EP3435770A1 true EP3435770A1 (en) 2019-02-06

Family

ID=58461317

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17714717.0A Withdrawn EP3435770A1 (en) 2016-03-31 2017-03-30 Production of milk with low lactose content

Country Status (2)

Country Link
EP (1) EP3435770A1 (en)
WO (1) WO2017167847A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE1026724B1 (en) * 2018-10-24 2020-05-28 Inex Nv Milk product with a reduced lactose content and a method for manufacturing the milk product

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013182686A1 (en) * 2012-06-08 2013-12-12 Dupont Nutrition Biosciences Aps Polypeptides having transgalactosylating activity

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990014423A1 (en) 1989-05-18 1990-11-29 The Infergene Company Microorganism transformation
WO1991000920A2 (en) 1989-07-07 1991-01-24 Unilever N.V. Process for preparing a protein by a fungus transformed by multicopy integration of an expression vector
DE69432543T2 (en) 1993-07-23 2003-12-24 Dsm N.V., Te Heerlen Selection marker gene-free recombinant strains: process for their preparation and the use of these strains
US6265186B1 (en) 1997-04-11 2001-07-24 Dsm N.V. Yeast cells comprising at least two copies of a desired gene integrated into the chromosomal genome at more than one non-ribosomal RNA encoding domain, particularly with Kluyveromyces
JP5303084B2 (en) 1997-04-11 2013-10-02 コニンクリーケ デーエスエム ナムローゼ フェンノートシャップ Gene conversion as a means to build industrial recombinant organisms
CN100390285C (en) 1998-05-19 2008-05-28 Dsm公司 Improvements in the in vivo production of cephalosporins
CN1331751A (en) 1998-12-22 2002-01-16 Dsm公司 Improved i(in vivo) prodn. of cephalosporins
KR20080045766A (en) 2000-05-26 2008-05-23 아를라 푸즈 에이엠비에이 Beta-galactosidase isolated from Bifidobacterium
US20100285175A1 (en) 2007-12-03 2010-11-11 Novozymes A/S Method for Producing a Dairy Product
AU2008333301B2 (en) 2007-12-04 2011-09-15 Shell Internationale Research Maatschappij B.V. Method and apparatus for cooling and/or liquefying a hydrocarbon stream
EP2997152A2 (en) 2013-05-14 2016-03-23 Novozymes A/S Process for simultaneous saccharfication and fermentation of whey permeate
EP3446569A1 (en) * 2013-12-11 2019-02-27 DuPont Nutrition Biosciences ApS A method for preparing a dairy product having a stable content of galacto-oligosaccharide(s)
AU2015226138B2 (en) * 2014-03-06 2018-11-22 Arla Foods Amba Lactose-reduced milk products containing galacto-oligosaccharides and monosaccharides and a method of production

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013182686A1 (en) * 2012-06-08 2013-12-12 Dupont Nutrition Biosciences Aps Polypeptides having transgalactosylating activity

Also Published As

Publication number Publication date
WO2017167847A1 (en) 2017-10-05

Similar Documents

Publication Publication Date Title
US12557825B2 (en) Lactose reduced dairy powder
AU2026201364A1 (en) Method for reducing lactose at high temperatures
EP3609910B1 (en) LACTASE ENZYMES WITH IMPROVED PROPERTIES
CN104334720A (en) Polypeptides with transgalactosylation activity
Mora et al. Characterization of urease genes cluster of Streptococcus thermophilus
AU2022205242A1 (en) Lactase enzymes with improved properties
Miyamoto et al. Distinctive proteolytic activity of cell envelope proteinase of Lactobacillus helveticus isolated from airag, a traditional Mongolian fermented mare's milk
CN109310101A (en) Fermented dairy products with reduced lactose content
Zhang et al. Purification and properties of heat-stable extracellular protease from Pseudomonads fluorescens BJ-10
AU2022206727A1 (en) Lactase enzymes with improved activity at low temperatures
US12435326B2 (en) Lactase enzymes with improved properties
Zarei et al. Identification of Pseudomonas jessenii and Pseudomonas gessardii as the most proteolytic Pseudomonas isolates in Iranian raw milk and their impact on stability of sterilized milk during storage
EP3435770A1 (en) Production of milk with low lactose content
WO2017167848A1 (en) Enzyme composition and preparation of a dairy product with improved properties
WO2017167849A1 (en) Enzyme composition and preparation of a dairy product with improved properties
Monnet et al. Selection and properties of Streptococcus thermophilus mutants deficient in urease
US20250008971A1 (en) Lactic acid bacterium, lactic acid bacterium starter, fermented milk, method for producing fermented milk, and method for screening lactic acid bacterium
Luesink et al. Regulation of the carbohydrate metabolism in Lactococcus lactis and other lactic acid bacteria
US12538929B2 (en) Production of lactase enzymes using altered regulation strains
Song et al. Isolation and analysis of salt response of Lactobacillus plantarum FS5-5 from Dajiang
CN118401115A (en) Method for producing milk-based products
Li et al. Characterization of a rolling-circle replication plasmid pLR1 from Lactobacillus plantarum LR1
JP6785765B2 (en) Dairy products
US20250324990A1 (en) Lactase enzymes with improved activity at low temperatures
RU2800427C2 (en) Lactase enzymes with improved activity at low temperatures

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20180919

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20221201

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20230613