IP Library › Granted Patent US 10,155,934
Granted Patent B2
US 10,155,934 · App. 15/679,586 · Granted Dec 18, 2018

Cytochrome P450 polypeptide with increased enzyme activity

Inventors: Marine Bertin (Paris, FR); Bruno Dumas (Paris, FR)
Assignee: SANOFI
C12N9/0079C12N9/0071C12P33/00
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Quick Facts
Patent No.
US 10,155,934
App. No.
15/679,586
Granted
Dec 18, 2018
Kind
B2
Abstract

The present invention pertains to an isolated P450 enzyme comprising or consisting of an amino acid sequence at least 80% identical to SEQ ID NO: 1, wherein said sequence comprises a threonine at position corresponding to position 225 and/or an aspartic acid mutation at position corresponding to position 289. The invention also concerns an isolated nucleic acid comprising a sequence encoding said enzyme, a vector comprising said nucleic acid, and a host cell containing said nucleic acid or said vector. Methods for preparing said enzyme and methods for producing steroid hormone precursors using the enzyme or the host cells featured in the invention are also provided.

Claims (23)

1. An isolated nucleic acid which comprises a nucleotide sequence encoding an isolated P450 enzyme comprising an amino acid sequence at least 97% identical to SEQ ID NO: 1, wherein said sequence comprises a threonine at a position corresponding to position 225 and/or an aspartic acid at a position corresponding to position 289.

2. A vector comprising a nucleic acid as defined in claim 1 which is operatively associated with expression control sequences.

3. The vector according to claim 2 , further comprising a nucleic acid sequence encoding adrenodoxin (Adx) and/or a nucleic acid sequence encoding adrenodoxin reductase (AdR).

4. A host cell containing a nucleic acid as defined in claim 1 .

5. The host cell according to claim 4 , which is a genetically engineered microorganism.

6. The host cell according to claim 4 which is Saccharomyces cerevisiae.

7. A genetically engineered microorganism capable of converting a substrate selected from the group consisting of polycyclic and unsaturated mono alcohols having an aliphatic side chain such as cholesterol, a cholesterol analogue and a cholesterol derivative, into a steroid hormone precursor, wherein said microorganism comprises a nucleic acid as defined in claim 1 , and optionally a nucleic acid sequence encoding adrenodoxin (Adx) and/or a nucleic acid sequence encoding adrenodoxin reductase (AdR).

8. An in vitro method for preparing the enzyme encoded by the nucleotide sequence as defined in claim 1 , said method comprising the steps of:

a) culturing a host cell containing the nucleic acid of claim 1 under conditions suitable to obtain expression of the enzyme; and

b) recovering the expressed enzyme.

9. The isolated nucleic acid according to claim 1 , comprising a sequence encoding an isolated P450 enzyme comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 3.

10. The isolated nucleic acid according to claim 9 , comprising a nucleotide sequence encoding an enzyme consisting of SEQ ID NO: 1.

11. A vector comprising the nucleic acid according to claim 9 , which is operatively associated with expression control sequences.

12. The vector according to claim 11 , further comprising a nucleic acid sequence encoding adrenodoxin (Adx) and/or a nucleic acid sequence encoding adrenodoxin reductase (AdR).

13. A host cell containing the nucleic acid according to claim 9 .

14. The host cell according to claim 13 , which is a genetically engineered microorganism.

15. The host cell according to claim 13 , which is Saccharomyces cerevisiae.

16. A genetically engineered microorganism capable of converting a substrate selected from the group consisting of polycyclic and unsaturated mono alcohols having an aliphatic side chain such as cholesterol, a cholesterol analogue and a cholesterol derivative, into a steroid hormone precursor, wherein said microorganism comprises a nucleic acid as defined in claim 9 , and optionally a nucleic acid sequence encoding adrenodoxin (Adx) and/or a nucleic acid sequence encoding adrenodoxin reductase (AdR).

17. An in vitro method for preparing the enzyme according to claim 9 , said method comprising the steps of:

a) culturing the host cell containing the nucleic acid under conditions suitable to obtain expression of the enzyme; and

b) recovering the expressed enzyme.

18. The isolated nucleic acid of claim 1 , comprising an amino acid sequence at least 98% or at least 99% identical to SEQ ID NO: 1.

19. An isolated nucleic acid which comprises a nucleotide sequence encoding an isolated P450 enzyme comprising or consisting of an amino acid sequence at least 98% identical to SEQ ID NO: 1, wherein said sequence comprises a threonine at a position corresponding to position 225 and/or an aspartic acid at a position corresponding to position 289.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 29, 2023
From: SANOFI
To: EUROAPI FRANCE
Reel/Frame 065978/0292 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 16, 2018
From: BERTIN, MARINE; DUMAS, BRUNO
To: SANOFI
Reel/Frame 044625/0935 →
Priority Claims (1)
EP 14305071 · Jan 20, 2014 · regional
Continuity (2)
Division 14601162 · Jan 20, 2015
Related Publication 20170342389A1 · Nov 30, 2017