Lipolytic enzyme for use in baking

US11510413B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11510413-B2
Application numberUS-202117337613-A
CountryUS
Kind codeB2
Filing dateJun 3, 2021
Priority dateFeb 20, 2017
Publication dateNov 29, 2022
Grant dateNov 29, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention relates to a polypeptide having lipolytic enzyme activity, selected from the group consisting of: (a) a polypeptide having at least 65% sequence identity to amino acids 21 to 309 of SEQ ID NO: 1; (b) a polypeptide encoded by a polynucleotide that hybridizes under medium stringency conditions with the polypeptide coding sequence of SEQ ID NO: 2; (c) a polypeptide encoded by a polynucleotide having at least 65% sequence identity to the polypeptide coding sequence of SEQ ID NO: 2; and (d) a fragment of the polypeptide of (a), (b) or (c) that has lipolytic enzyme activity.

First claim

Opening claim text (preview).

The invention claimed is: 1. A recombinant microbial host cell transformed with a polynucleotide encoding a polypeptide having lipolytic activity, wherein the polynucleotide is operably linked to one or more control sequences that direct the production of the polypeptide in the recombinant host cell, and wherein the polypeptide comprises an amino acid sequence having at least 80% sequence identity to the sequence of amino acids 21 to 309 of SEQ ID NO: 1. 2. A method of producing a polypeptide having lipolytic activity, comprising cultivating the recombinant host cell of claim 1 under conditions conducive for production of the polypeptide. 3. The method of claim 2 , further comprising recovering the polypeptide. 4. The method of claim 2 , wherein the recombinant host cell is a Gram-positive or Gram-negative bacterium selected from the group consisting of Bacillus, Clostridium, Enterococcus, Geobacillus, Lactobacillus, Lactococcus, Oceanobacillus, Staphylococcus, Streptococcus, Streptomyces, Campylobacter, Escherichia coli, Flavobacterium, Fusobacterium, Helicobacter, Ilyobacter, Neisseria, Pseudomonas, Salmonella , and Ureaplasma. 5. The method of claim 4 , wherein the recombinant host cell is a Bacillus cell selected from the group consisting of Bacillus alkalophilus, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus clausii, Bacillus coagulans, Bacillus firmus, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus pumilus, Bacillus stearothermophilus, Bacillus subtilis , and Bacillus thuringiensis cells. 6. The method of claim 2 , wherein the recombinant host cell is a yeast cell selected from the group consisting of Candida, Hansenula, Kluyveromyces, Pichia, Saccharomyces, Schizosaccharomyces , and Yarrowia cells. 7. The method of claim 2 , wherein the recombinant host cell is a filamentous fungal cell selected from the group consisting of Acremonium, Aspergillus, Aureobasidium, Bjerkandera, Ceriporiopsis, Chrysosporium, Coprinus, Coriolus, Cryptococcus, Filibasidium, Fusarium, Humicola, Magnaporthe, Mucor, Myceliophthora, Neocallimastix, Neurospora, Paecilomyces, Penicillium, Phanerochaete, Phlebia, Piromyces, Pleurotus, Schizophyllum, Talaromyces, Thermoascus, Thielavia, Tolypocladium, Trametes , and Trichoderma cells. 8. The method of claim 2 , wherein the polypeptide comprises the amino acid sequence G-H-S-L-G (SEQ ID NO: 5). 9. The method of claim 2 , wherein the polypeptide comprises an amino acid sequence having at least 85% sequence identity to the sequence of amino acids 21 to 309 of SEQ ID NO: 1. 10. The method of claim 2 , wherein the polypeptide comprises an amino acid sequence having at least 90% sequence identity to the sequence of amino acids 21 to 309 of SEQ ID NO: 1. 11. The method of claim 2 , wherein the polypeptide comprises an amino acid sequence having at least 95% sequence identity to the sequence of amino acids 21 to 309 of SEQ ID NO: 1. 12. The method of claim 2 , wherein the polypeptide comprises an amino acid sequence having at least 97% sequence identity to the sequence of amino acids 21 to 309 of SEQ ID NO: 1. 13. The method of claim 2 , wherein the polypeptide comprises the amino acid sequence of amino acids 21 to 309 of SEQ ID NO: 1. 14. The method of claim 2 , wherein the polypeptide comprises the amino acid sequence of amino acids 21 to 309 of SEQ ID NO: 6. 15. The method of claim 2 , wherein the polypeptide comprises the amino acid sequence of amino acids 21 to 309 of SEQ ID NO: 7. 16. The method of claim 2 , wherein the polypeptide comprises the amino acid sequence of amino acids 21 to 309 of SEQ ID NO: 8. 17. The method of claim 2 , wherein the polypeptide comprises the amino acid sequence of amino acids 21 to 309 of SEQ ID NO: 9. 18. The method of claim 2 , wherein the polypeptide is a fragment of the sequence of amino acids 21 to 309 of SEQ ID NO: 1, wherein the fragment has lipase activity. 19. The method of claim 2 , wherein the polypeptide has lipase and phospholipase activity. 20. The recombinant host cell of claim 1 , wherein the one or more control sequences is heterologous to the polynucleotide.

Assignees

Inventors

Classifications

  • A21D8/042Primary

    with enzymes · CPC title

  • Dough mixes; Baking or bread improvers; Premixes · CPC title

  • Carboxylic ester hydrolases (3.1.1) · CPC title

  • Batters, dough or mixtures before baking · CPC title

  • Triglyceride splitting, e.g. by means of lipase · CPC title

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What does patent US11510413B2 cover?
The present invention relates to a polypeptide having lipolytic enzyme activity, selected from the group consisting of: (a) a polypeptide having at least 65% sequence identity to amino acids 21 to 309 of SEQ ID NO: 1; (b) a polypeptide encoded by a polynucleotide that hybridizes under medium stringency conditions with the polypeptide coding sequence of SEQ ID NO: 2; (c) a polypeptide encoded by…
Who is the assignee on this patent?
Novozymes As, Puratos Nv/Sa
What technology area does this patent fall under?
Primary CPC classification A21D8/042. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Nov 29 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).