Method for reconstructing aspergillus niger to increase citrate production

US10618940B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10618940-B2
Application numberUS-201815868136-A
CountryUS
Kind codeB2
Filing dateJan 11, 2018
Priority dateJan 12, 2017
Publication dateApr 14, 2020
Grant dateApr 14, 2020

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The invention discloses a method for increasing citrate production from genome reconstructed Aspergillus niger. The method is to insert a gene of low affinity glucose transporter, LGT1, to genome of A. niger. The expression level of LGT1 is under control of promoter Pgas. The genome reconstructed A. niger is tolerant to higher fermentation temperature and lower pH than that of the parental strain. Moreover, the production, yield and purity of product from reconstructed A. niger are higher than that of parental strain, and the fermentation time is shorter.

First claim

Opening claim text (preview).

What is claimed is: 1. A recombinant Aspergillus niger strain, comprising: a genome comprising an inserted low affinity glucose transporter gene LGT1, wherein the glucose transporter gene LGT1 transporter is under the control of a Pgas promoter, wherein the glucose transporter gene LGT1 sequence is SEQ ID NO:1, wherein the Pgas promoter sequence is SEQ ID NO:3, and wherein the A. niger strain produces a higher relative amount of citrate as compared with a wild type A. niger strain grown under identical conditions. 2. The recombinant A. niger strain according to claim 1 , wherein the glucose transporter gene LGT1 encodes a protein having the sequence SEQ ID NO:2. 3. The recombinant A. niger strain according to claim 1 , wherein the Pgas promoter controlling the expression level of LGT1 is induced by a low pH of between pH 2.0 and pH 3.5. 4. A expression cassette of LGT1 comprising a promoter of Pgas, LGT1 gene and terminator of trp in order of Pgas-LGT1-trp. 5. The expression cassette in claim 4 , wherein a sequence of Pgas is set forth in SEQ ID NO:3, an amino acid sequence of LGT1 is set forth in SEQ ID NO:2, and a sequence of trp terminator is set forth in SEQ ID NO:6. 6. The recombinant Aspergillus niger strain of claim 1 , wherein the gene sequence of glucose transporter gene LGT1 and promoter Pgas are encoded onto an expression cassette transformed into the A. niger strain. 7. The recombinant Aspergillus niger strain of claim 6 , wherein the expression cassette further comprises at least one trp terminator sequence of SEQ ID NO:6. 8. The recombinant Aspergillus niger strain of claim 6 , wherein the expression cassette further comprises a gpdA promoter sequence of SEQ ID NO:4. 9. The recombinant Aspergillus niger strain of claim 6 , wherein the expression cassette further comprises a hygromycin resistance (hph) gene sequence of SEQ ID NO:5. 10. The recombinant Aspergillus niger strain of claim 6 , wherein the expression cassette encodes a trp terminator sequence of SEQ ID NO:6, a gpdA promoter sequence of SEQ ID NO:4, and an hgh gene sequence of SEQ ID NO:5. 11. The recombinant Aspergillus niger strain of claim 10 , wherein the expression cassette sequences are in the order of gpdA-hph-trp and Pgas-LGT1-trp. 12. The recombinant Aspergillus niger strain of claim 1 , wherein the A. niger strain is derived from A. niger strain H915-1. 13. The recombinant Aspergillus niger strain of claim 1 , wherein the amount of citrate produced by the A. niger strain is at least 6.5% higher under identical conditions than a corresponding wild type Aspergillus niger strain. 14. The recombinant Aspergillus niger strain of claim 1 , wherein the amount of citrate produced by the A. niger strain is at least 40.3% higher under identical conditions than a corresponding wild type Aspergillus niger strain. 15. A method for the reconstruction of reconstructed A. niger mentioned in claim 1 , comprising the following steps: (1) constructing an expression cassette of LGT1 with Pgas-LGT1-trp; (2) Constructing a resistant gene expression cassette gpdA-hph-trp; (3) inserting expression cassette in step (1) and (2) into A. niger , screening resistant strains and confirming reconstructed strains with PCR. 16. The method in claim 15 , wherein a sequence of gpdA promoter in resistant gene cassette is set forth in SEQ ID NO: 4. 17. The method in claim 15 , wherein a sequence of resistant gene hph in resistant gene cassette is set forth in SEQ ID NO: 5. 18. A method of expressing citric acid from Aspergillus niger , which comprises: incubating an A. niger strain in growth medium comprising malt extract and tryptone at 35° C. for seven days to generate conidia, wherein the A. niger strain comprises a genome comprising a low affinity glucose transporter gene LGT1, wherein the glucose transporter gene LGT1 transporter is under the control of a Pgas promoter, wherein the glucose transporter gene LGT1 sequence is SEQ ID NO:1, and wherein the Pgas promoter sequence is SEQ ID NO:3, harvesting the conidia, inoculating seed medium with the conidia at a density of 10 6 per mL to generate a seed culture, wherein the seed medium comprises corn starch medium comprising a total sugar concentration of 10% and a total nitrogen concentration of 0.2%, growing the conidia in the seed medium at 37° C. for 24 hours at pH 3.5, inoculating a fermentation medium with the seed culture at 1/10 volume, incubating the fermentation medium for 72 hours at 42° C. at pH 2.0, centrifuging the fermented fermentation medium and discarding mycelium to obtain citric acid. 19. The method of claim 18 , wherein the A. niger strain produces a higher relative amount of citrate as compared with a wild type A. niger strain grown under identical conditions. 20. The method of claim 18 , wherein the A. niger strain produces between 6.5% and 40.3% more citrate as compared with a wild type A. niger strain under identical conditions.

Assignees

Inventors

Classifications

  • for fungi · CPC title

  • C07K14/38Primary

    from Aspergillus · CPC title

  • Polyesters of hydroxy carboxylic acids · CPC title

  • Tricarboxylic acids, e.g. citric acid · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US10618940B2 cover?
The invention discloses a method for increasing citrate production from genome reconstructed Aspergillus niger. The method is to insert a gene of low affinity glucose transporter, LGT1, to genome of A. niger. The expression level of LGT1 is under control of promoter Pgas. The genome reconstructed A. niger is tolerant to higher fermentation temperature and lower pH than that of the parental stra…
Who is the assignee on this patent?
Univ Jiangnan, Jiangsu Guoxin Union Energy Co Ltd
What technology area does this patent fall under?
Primary CPC classification C07K14/38. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 14 2020 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).