IP Library Granted Patent US 11,572,564
Granted Patent B2
US 11,572,564 · App. 15/018,736 · Granted Feb 7, 2023

Microorganisms for producing 1,4-butanediol and methods related thereto

Inventor: Wei Niu (Lincoln, NE)
Assignee: Genomatica, Inc.
C12N15/52C12N9/0008C12P7/16C12P7/18C12P7/42C12Y102/99006Y02E50/10
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Quick Facts
Patent No.
US 11,572,564
App. No.
15/018,736
Granted
Feb 7, 2023
Kind
B2
Abstract

The invention provides non-naturally occurring microbial organisms comprising a 1,4-butanediol (BDO), 4-hydroxybutyryl-CoA, 4-hydroxybutanal or putrescine pathway comprising at least one exogenous nucleic acid encoding a BDO, 4-hydroxybutyryl-CoA, 4-hydroxybutanal or putrescine pathway enzyme expressed in a sufficient amount to produce BDO, 4-hydroxybutyryl-CoA, 4-hydroxybutanal or putrescine and further optimized for expression of BDO. The invention additionally provides methods of using such microbial organisms to produce BDO, 4-hydroxybutyryl-CoA, 4-hydroxybutanal or putrescine.

Claims (3)

1. An engineered isolated carboxylic acid reductase (CAR) variant, comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO:101 and having an amino acid substitution selected from E16K; Q95L; L100M; A1011T; K823E; T941S; D198E; G446C; S392N; F699L; V883I; F467S; T987S; R12H; V295G; V295A; V295S; V295T; V295C; V295L; V295I; V295M; V295P; V295F; V295Y; V295W; V295D; V295E; V295N; V295Q; V295H; V295K; V295R; M296G; M296A; M296S; M296T; M296C; M296V; M296L; M296I; M296P; M296F; M296Y; M296W; M296D; M296E; M296N; M296Q; M296H; M296K; M296R; G297A; G297S; G297T; G297C; G297V; G297L; G297I; G297M; G297P; G297F; G297Y; G297W; G297D; G297E; G297N; G297Q; G297H; G297K; G297R; G391A; G391S; G391T; G391C; G391V; G391L; G391I; G391M; G391P; G391F; G391Y; G391W; G391D; G391E; G391N; G391Q; G391H; G391K; G391R; G421A; G421S; G421T; G421C; G421V; G421L; G421I G421M; G421P; G421F; G421Y; G421W; G421D; G421E; G421N; G421Q; G421H; G421K; G421R; D413G; D413A; D413S; D413T; D413C; D413V; D413L; D413I; D413M; D413P; D413F; D413Y; D413W; D413N; D413Q; D413H; D413K; D413R; G414A; G414S; G414T; G414C; G414V; G414L; G414I; G414M; G414P; G414F; G414Y; G414W; G414D; G414E; G414N; G414Q; G414H; G414K; G414R; Y415G; Y415A; Y415S; Y415T; Y415C; Y415V; Y415L; Y415I; Y415M; Y415P; Y415F; Y415W; Y415D; Y415E; Y415N; Y415Q; Y415H; Y415K; Y415R; G416A; G416S; G416T; G416C; G416V; G416L; G416I; G416M; G416P; G416F; G416Y; G416W; G416D; G416E; G416N; G416Q; G416H; G416K; G416R; S417G; S417A; S417T; S417C; S417V S417L; S417I; S417M; S417P; S417F; S417Y; S417W; S417D; S417E; S417N; S417Q; S417H; S417K; and S417R, corresponding to the amino acid positions of the sequence of SEQ ID NO:101, or combinations thereof, wherein said engineered isolated carboxylic acid reductase catalyzes the conversion of a carboxylic acid to its aldehyde, and wherein said engineered isolated CAR is not naturally-occurring.

2. An engineered isolated carboxylic acid reductase (CAR) variant comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO:101 and having an amino acid substitution at position V295, M296, G297, G391, G421, G414, Y415, G416 or 5417 corresponding to the amino acid positions of the sequence of SEQ ID NO:101, wherein said engineered isolated carboxylic acid reductase variant catalyzes the conversion of a carboxylic acid to its aldehyde, and wherein said engineered isolated CAR is not naturally-occurring.

3. An engineered isolated carboxylic acid reductase (CAR) variant comprising the amino acid sequence of SEQ ID NO:101 and having an amino acid substitution in SEQ ID NO:101 selected from the group consisting of E16K; Q95L; L100M; A1011T; K823E; T941S; H15Q; D198E; G446C; S392N; F699L; V883I; F467S; T987S; R12H; V295G; V295A; V295S; V295T; V295C; V295L; V295I; V295M; V295P; V295F; V295Y; V295W; V295D; V295E; V295N; V295Q; V295H; V295K; V295R; M296G; M296A; M296S; M296T; M296C; M296V; M296L; M296I; M296P; M296F; M296Y; M296W; M296D; M296E; M296N; M296Q; M296H; M296K; M296R; G297A; G297S; G297T; G297C; G297V; G297L; G297I; G297M; G297P; G297F; G297Y; G297W; G297D; G297E; G297N; G297Q; G297H; G297K; G297R; G391A; G391S; G391T; G391C; G391V; G391L; G391I; G391M; G391P; G391F; G391Y; G391W; G391D; G391E; G391N; G391Q; G391H; G391K; G391R; G421A; G421S; G421T; G421C; G421V; G421L; G421I G421M; G421P; G421F; G421Y; G421W; G421D; G421E; G421N; G421Q; G421H; G421K; G421R; D413G; D413A; D413S; D413T; D413C; D413V; D413L; D413I; D413M; D413P; D413F; D413Y; D413W; D413E; D413N; D413Q; D413H; D413K; D413R; G414A; G414S; G414T; G414C; G414V; G414L; G414I; G414M; G414P; G414F; G414Y; G414W; G414D; G414E; G414N; G414Q; G414H; G414K; G414R; Y415G; Y415A; Y415S; Y415T; Y415C; Y415V; Y415L; Y415I; Y415M; Y415P; Y415F; Y415W; Y415D; Y415E; Y415N; Y415Q; Y415H; Y415K; Y415R; G416A; G416S; G416T; G416C; G416V; G416L; G416I; G416M; G416P; G416F; G416Y; G416W; G416D; G416E; G416N; G416Q; G416H; G416K; G416R; S417G; S417A; S417T; S417C; S417V S417L; S417I; 5417M; S417P; S417F; S417Y; S417W; S417D; S417E; S417N; S417Q; S417H; S417K; and S417R, wherein said engineered isolated carboxylic acid reductase variant catalyzes the conversion of a carboxylic acid to its aldehyde, and wherein said engineered isolated CAR is not naturally-occurring.

Assignments (4)
SECURITY INTEREST Recorded Feb 10, 2026
From: GENOMATICA, INC.
To: AGAIN BIO APS
Reel/Frame 074708/0001 →
SECURITY INTEREST Recorded Dec 9, 2025
From: GENOMATICA, INC.
To: NOVO HOLDINGS A/S, AS COLLATERAL AGENT
Reel/Frame 073915/0027 →
SECURITY INTEREST Recorded Jun 2, 2025
From: GENOMATICA, INC.
To: OXFORD FINANCE LLC
Reel/Frame 071471/0770 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 19, 2022
From: NIU, WEI
To: GENOMATICA INC.
Reel/Frame 062146/0493 →
Continuity (4)
Continuation 13530053 · Jun 21, 2012
Provisional Application 61502837 · Jun 29, 2011
Provisional Application 61500120 · Jun 22, 2011
Related Publication 20160264978A1 · Sep 15, 2016