Isolated DNA encoding protein having improved stability

US9315782B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9315782-B2
Application numberUS-201113574458-A
CountryUS
Kind codeB2
Filing dateJan 19, 2011
Priority dateJan 20, 2010
Publication dateApr 19, 2016
Grant dateApr 19, 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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  5. First independent claim

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Abstract

Official abstract text for this publication.

Water-forming NADH oxidase derived from Streptococcus mutans should be further improved in terms of stability for practical use in industrial production. An object of the present invention is to provide an enzyme that is obtained through modification of a water-forming NADH oxidase, which is useful as an NAD+ regeneration system for stereoselective oxidation catalyzed by an oxidoreductase, by protein engineering techniques so that the enzyme can withstand long-term use without exhibiting a reduction of its activity for the regeneration of NAD+, that is, an enzyme having improved stability, and to provide a method for efficiently producing a useful substance such as an optically active alcohol or amino acid. The present invention relates to an enzyme modification method that can improve the stability of water-forming NADH oxidase derived from Streptococcus mutans by appropriately introducing mutation.

First claim

Opening claim text (preview).

The invention claimed is: 1. An isolated DNA encoding a protein which has NADH oxidase activity or NADPH oxidase activity or both and has improved stability compared to the protein having the amino acid sequence of SEQ ID NO: 1, and wherein said protein has an amino acid sequence that has at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 1 and further contains at least one amino acid substitution selected from (a) to (g): (a) a substitution of an amino acid residue at a position corresponding to position 42 of SEQ ID NO: 1 with an amino acid having a side-chain surface area of 100 to 200 Å 2 ; (b) a substitution of an amino acid residue at a position corresponding to position 46 of SEQ ID NO:1 with a neutral amino acid having a side-chain surface area of 100 to 150 Å 2 or an acidic amino acid having a side-chain surface area of 100 to 150 Å 2 ; (c) a substitution of an amino acid residue at a position corresponding to position 96 of SEQ ID NO:1 with a basic amino acid; (d) a substitution of an amino acid residue at a position corresponding to position 172 of SEQ ID NO: 1 with an amino acid having a smaller side-chain surface area than Tyr; (e) a substitution of an amino acid residue at a position corresponding to position 196 of SEQ ID NO:1 with a basic amino acid; (f) a substitution of an amino acid residue at a position corresponding to position 312 of SEQ ID NO: 1 with an amino acid having a larger side-chain surface area than Ala; and (g) a substitution of an amino acid residue at a position corresponding to position 371 of SEQ ID NO: 1 with an aliphatic amino acid, an acidic amino acid, or an amino acid having a hydroxyl group-bearing side chain. 2. A vector comprising the DNA according to claim 1 . 3. A transformant obtained by transformation of a host cell with the vector according to claim 2 . 4. A culture of the transformant according to claim 3 . 5. The isolated DNA according to claim 1 , wherein the amino acid sequence contains at least one amino acid substitution selected from (a) to (g): (a) a substitution of an amino acid residue at a position corresponding to position 42 of SEQ ID NO:1 with Met; (b) a substitution of an amino acid residue at a position corresponding to position 46 of SEQ ID NO:1 with Ile; (c) a substitution of an amino acid residue at a position corresponding to position 96 of SEQ ID NO:1 with Arg or His; (d) a substitution of an amino acid residue at a position corresponding to position 172 of SEQ ID NO:1 with Ala or Ser; (e) a substitution of an amino acid residue at a position corresponding to position 196 of SEQ ID NO:1 with His; (f) a substitution of an amino acid residue at a position corresponding to position 312 of SEQ ID NO:1 with Ile; and (g) a substitution of an amino acid residue at a position corresponding to position 371 of SEQ ID NO:1 with Ala, Val, Ile, Glu, Ser, Thr, or Tyr. 6. An isolated DNA that encodes a protein which comprises an amino acid sequence identical to SEQ ID NO: 1 except for one or more substitutions selected from the group consisting of: (a) a substitution of Leu at position 42 of SEQ ID NO: 1 with an amino acid having a side-chain surface area of 100 to 200 Å 2 ; (b) a substitution of Met at position 46 of SEQ ID NO: 1 with a neutral amino acid having a side-chain surface area of 100 to 150 Å 2 or an acidic amino acid having a side-chain surface area of 100 to 150 Å 2 ; (c) a substitution of Asn at position 96 of SEQ ID NO: 1 with a basic amino acid; (d) a substitution of Tyr at position 172 of SEQ ID NO: 1 with an amino acid having a smaller side-chain surface area than Tyr; (e) a substitution of Thr at position 196 of SEQ ID NO: 1 with a basic amino acid; (f) a substitution of Ala at positon 312 with an amino acid having a larger side-chain surface area than Ala; and (g) a substitution of Phe at position 371 of SEQ ID NO: 1 with an aliphatic amino acid, an acidic amino acid, or an amino acid having a hydroxyl group-bearing side chain. 7. The isolated DNA according to claim 6 wherein said protein comprises an amino acid sequence identical to SEQ ID NO: 1 except for one or more substitutions selected from the group consisting of: (a) a substitution of Leu at position 42 of SEQ ID NO: 1 with Met; (b) a substitution of Met at position 46 of SEQ ID NO: 1 with Ile; (c) a substitution of Asn at position 96 of SEQ ID NO: 1 with Arg or His; (d) a substitution of Tyr at position 172 of SEQ ID NO: 1 with Ala or Ser; (e) a substitution of Thr at position 196 of SEQ ID NO: 1 with His; (f) a substitution of Ala at positon 312 with Ile; and (g) a substitution of Phe at position 371 of SEQ ID NO: 1 with Ala, Val, Ile, Glu, Ser, Thr, or Tyr. 8. An isolated DNA encoding a protein having an amino acid sequence selected from the amino acid sequences of SEQ ID Nos:2 and 4 to 19.

Assignees

Inventors

Classifications

  • C12N9/0065Primary

    acting on hydrogen peroxide as acceptor (1.11) · CPC title

  • acting on NADH or NADPH (1.6) · CPC title

  • with oxygen as acceptor (1.6.3) · CPC title

  • Alpha- or beta- amino acids {(other amino acids C12P13/005)} · CPC title

  • Dinucleotides, e.g. nicotineamide-adenine dinucleotide phosphate · CPC title

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What does patent US9315782B2 cover?
Water-forming NADH oxidase derived from Streptococcus mutans should be further improved in terms of stability for practical use in industrial production. An object of the present invention is to provide an enzyme that is obtained through modification of a water-forming NADH oxidase, which is useful as an NAD+ regeneration system for stereoselective oxidation catalyzed by an oxidoreductase, by…
Who is the assignee on this patent?
Yoshida Shinichi, Iwasaki Akira, Washida Motohisa, and 4 more
What technology area does this patent fall under?
Primary CPC classification C12N9/0065. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 19 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).