Method of improving acid decarboxylase activity in vitro under alkaline pH

US12325872B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12325872-B2
Application numberUS-202318300251-A
CountryUS
Kind codeB2
Filing dateApr 13, 2023
Priority dateNov 24, 2016
Publication dateJun 10, 2025
Grant dateJun 10, 2025

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  5. First independent claim

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Abstract

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This invention provides acid decarboxylase-prion subunit fusion polypeptides, nucleic acid sequences, expression vectors, and host cells expression such fusion polypeptides to produce various amino acids and derivatives of the amino acids such as polyamines.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of improving Escherichia coli lysine decarboxylase CadA polypeptide activity by at least 5% in vitro under alkaline pH comprising fusing a prion subunit to the carboxyl terminus of the Escherichia coli lysine decarboxylase CadA polypeptide, wherein the prion subunit has at least 95% identity to the amino acid sequence of the prion subunit region of any one of SEQ ID NOS: 7, 8, 11, 12, 13, 14, 15, 17, or 19, and the Escherichia coli lysine decarboxylase CadA polypeptide has the amino acid sequence of SEQ ID NO: 2 or a biologically active fragment thereof that has lysine decarboxylase CadA polypeptide activity and has at least 95% amino acid sequence identity to SEQ ID NO: 2, and wherein the lysine decarboxylase CadA polypeptide activity is assessed by measuring the production of cadaverine and lysine Produced by a host cell that expresses the lysine decarboxylase cadA polypeptide fused to the prion subunit and a control cell that expresses the acid decarboxylase protein, but is not fused to the prion subunit, under identical conditions. 2. The method of claim 1 , wherein the prion subunit is at least 50 amino acids in length, but 500 amino acids or fewer in length. 3. The method of claim 1 , wherein the prion subunit comprises an amino acid composition having at least 20% glutamine and/or asparagine residues. 4. The method of claim 1 , wherein the prion subunit is joined at the carboxyl terminus to a BST fragment, λCI fragment, or RecA fragment. 5. The method of claim 1 , wherein the prion subunit is at least 75 amino acids in length, but 500 amino acids or fewer in length. 6. The method of claim 1 , wherein the prion subunit is at least 100 amino acids in length, but 500 amino acids or fewer in length.

Assignees

Inventors

Classifications

  • Lysine decarboxylase (4.1.1.18) · CPC title

  • Vectors or expression systems specially adapted for E. coli · CPC title

  • Fusion polypeptide · CPC title

  • C07K14/47Primary

    from mammals · CPC title

  • C12N9/88Primary

    Lyases (4.) · CPC title

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What does patent US12325872B2 cover?
This invention provides acid decarboxylase-prion subunit fusion polypeptides, nucleic acid sequences, expression vectors, and host cells expression such fusion polypeptides to produce various amino acids and derivatives of the amino acids such as polyamines.
Who is the assignee on this patent?
Cathay Biotech Inc, Cibt America Inc
What technology area does this patent fall under?
Primary CPC classification C07K14/47. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 10 2025 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).