Modified leucine dehydrogenase

US9453206B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9453206-B2
Application numberUS-201615133599-A
CountryUS
Kind codeB2
Filing dateApr 20, 2016
Priority dateMar 30, 2012
Publication dateSep 27, 2016
Grant dateSep 27, 2016

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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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Abstract

Official abstract text for this publication.

The present invention provides a means and method useful for measurement of a total branched-chain amino acid concentration. Specifically, the present invention provides a modified enzyme in which at least one amino acid residue is mutated so as to improve a property of a leucine dehydrogenase which is associated with the measurement of the total branched-chain amino acids, such as, for example, substrate specificities of leucine dehydrogenase for total branched-chain amino acids, activity of leucine dehydrogenase for any branched-chain amino acids, and thermal stability of leucine dehydrogenase; and a method of analyzing the total branched-chain amino acids, comprising measuring the total branched-chain amino acids contained in a test sample using the modified enzyme.

First claim

Opening claim text (preview).

The invention claimed is: 1. A modified leucine dehydrogenase enzyme comprising at least one amino acid mutation as compared to a non-modified leucine dehydrogenase enzyme, wherein said modified leucine dehydrogenase is improved in one or more properties selected from the group consisting of: (a) substrate specificities for L-leucine, L-isoleucine and L-valine; (b) activity for any branched-chain amino acid; (c) thermal stability, and (d) combinations thereof, wherein said modified leucine dehydrogenase is selected from the group consisting of: (A) a protein comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 4, SEQ ID NO: 6, and SEQ ID NO: 8; but having a substitution of isoleucine in the TGI motif with an amino acid selected from the group consisting of methionine, arginine, histidine, phenylalanine, leucine, lysine, cysteine, tyrosine, alanine, glycine, serine, asparagine, and tryptophan, (B) a protein comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 4, SEQ ID NO: 6, and SEQ ID NO: 8; but having a substitution of isoleucine in the GVI motif with an amino acid selected from the group consisting of phenylalanine, histidine, asparagine, tyrosine, leucine, lysine, glutamine, arginine, aspartic acid, threonine, glutamic acid, serine, cysteine, alanine, glycine, valine, tryptophan, and methionine, (C) a protein comprising the amino acid sequence selected from the group consisting of SEQ ID NO: 4, SEQ ID NO: 6, and SEQ ID NO: 8; but having a substitution of isoleucine in the TGI motif with an amino acid selected from the group consisting of methionine, arginine, histidine, phenylalanine, leucine, lysine, cysteine, tyrosine, alanine, glycine, serine, asparagine, and tryptophan; and a substitution of isoleucine in the GVI motif with an amino acid selected from the group consisting of phenylalanine, histidine, asparagine, tyrosine, leucine, lysine, glutamine, arginine, aspartic acid, threonine, glutamic acid, serine, cysteine, alanine, glycine, valine, tryptophan, and methionine, and (D) a protein as described in (A), (B), or (C) above, but also having one to ten additional mutations of amino acid residues. 2. A method of analyzing branched-chain amino acids, comprising measuring all branched-chain amino acids contained in a test sample using the modified leucine dehydrogenase enzyme according to claim 1 . 3. The method according to claim 2 , comprising mixing the test sample with nicotinamide adenine dinucleotide (NAD + ) and detecting NADH formed from NAD + by an action of the modified leucine dehydrogenase enzyme. 4. A kit for analyzing branched-chain amino acids, comprising the modified enzyme according to claim 1 . 5. The kit for analyzing branched-chain amino acids according to claim 4 , further comprising at least one of a buffer solution or a buffer salt for a reaction and nicotinamide adenine dinucleotide (NAD + ).

Assignees

Inventors

Classifications

  • C12N9/0016Primary

    with NAD or NADP as acceptor (1.4.1) · CPC title

  • Leucine dehydrogenase (1.4.1.9) · CPC title

  • involving dehydrogenase · CPC title

  • Alanine; Leucine; Isoleucine; Serine; Homoserine · CPC title

  • with a definite EC number (1.4.1.-) · CPC title

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What does patent US9453206B2 cover?
The present invention provides a means and method useful for measurement of a total branched-chain amino acid concentration. Specifically, the present invention provides a modified enzyme in which at least one amino acid residue is mutated so as to improve a property of a leucine dehydrogenase which is associated with the measurement of the total branched-chain amino acids, such as, for example…
Who is the assignee on this patent?
Ajinomoto Kk
What technology area does this patent fall under?
Primary CPC classification C12N9/0016. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 27 2016 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).