Highly stereoselective biosynthesis of (R)-α-hydroxy carboxylic acids through rationally re-designed mutation of D-lactate dehydrogenase. - Wikidata - awgldk - TriplyDB

Highly stereoselective biosynthesis of (R)-α-hydroxy carboxylic acids through rationally re-designed mutation of D-lactate dehydrogenase.

Highly stereoselective biosynthesis of (R)-α-hydroxy carboxylic acids through rationally re-designed mutation of D-lactate dehydrogenase.

http://www.wikidata.org/entity/Q33804917

about

Efficient production of enantiomerically pure D-phenyllactate from phenylpyruvate by structure-guided design of an engineered D-lactate dehydrogenase.Efficient production of (R)-2-hydroxy-4-phenylbutyric acid by using a coupled reconstructed D-lactate dehydrogenase and formate dehydrogenase system.

P2860

Q30386149-52C515CF-3575-41D7-905B-5A92FD84E95D Q34000216-79821DC3-935C-4606-9A26-3A7109CD1910

P2860

Highly stereoselective biosynthesis of (R)-α-hydroxy carboxylic acids through rationally re-designed mutation of D-lactate dehydrogenase.

http://www.wikidata.org/entity/Q33804917

description

2013 nî lūn-bûn

@nan

2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Highly stereoselective biosynt ...... on of D-lactate dehydrogenase.

@ast

Highly stereoselective biosynt ...... on of D-lactate dehydrogenase.

@en

type

label

Highly stereoselective biosynt ...... on of D-lactate dehydrogenase.

@ast

Highly stereoselective biosynt ...... on of D-lactate dehydrogenase.

@en

prefLabel

Highly stereoselective biosynt ...... on of D-lactate dehydrogenase.

@ast

Highly stereoselective biosynt ...... on of D-lactate dehydrogenase.

@en

P1433

Q33804917-74DB25D5-0219-4F2B-AD59-8E9E75B0B820

P1476

Q33804917-8B3099A9-B06E-404D-A504-3C074650BDFB

P2093

Q33804917-687FE297-E005-4BBD-BDAE-329DA2F4FA52

Q33804917-68EAFC08-CE79-429A-BC68-3B7F47D7EAA0

Q33804917-749742BA-B9FB-44B7-BDA4-652E4BD46BBD

Q33804917-B158E0C7-C353-4ABF-8645-6AE202162F56

Q33804917-F4F1A259-52BA-44BF-83D8-55D6A52B172A

P2860

Q33804917-0A22C3EB-5BC8-4D1C-9AEF-31C927411988

Q33804917-123D50D5-F671-4B21-B930-78B52B6D5321

Q33804917-1538AD5F-F568-4007-B2A2-AB0DBA78514C

Q33804917-1EA6CECE-41DA-4175-AB9F-378A7E18D947

Q33804917-277D863A-2670-4B6C-898D-654E60B4E0F0

Q33804917-34ACDA4D-3363-4EE9-BE90-FE8A688791BC

Q33804917-373AB630-993D-4077-9E08-C5011F269689

Q33804917-52A7B49F-256B-4B6C-86EC-494D770957DF

Q33804917-586F3B44-9972-4FBF-8D93-701964B034B4

Q33804917-5D855C58-E06E-4256-AF51-2934A7C9F1F6

P2888

Q33804917-10BC943C-4AF7-48DB-90E9-4084F0263B71

P304

Q33804917-49FBE93B-3583-4FB7-A940-C07881A03F43

P31

Q33804917-A6159A2A-A541-4F65-8527-4F7E7DD63B60

P356

Q33804917-C21CA30C-D1D7-49C9-855C-CDBA68DB9D9D

P407

Q33804917-2006A802-3855-4323-8D61-B378FE11FE2D

P478

Q33804917-67F22F1F-3F7C-4826-8666-11730D0F092C

P50

Q33804917-2BE476C5-25DE-4672-9A83-75A59F0E357A

Q33804917-C0B00C85-BE20-4BCA-9DE0-B7FDF637CBB5

P577

Q33804917-B28F1029-DF68-4B0A-8401-444E36C19335

P5875

Q33804917-4C091703-F50D-4A6F-8EDB-5283961051D4

P6179

Q33804917-612E3338-FE2C-46EA-9681-2C07C38A8E18

P698

Q33804917-1AAEE2EA-012A-4711-8433-770FF544EEA8

P921

Q33804917-D97D2D35-1754-43CF-BEF3-CDCDE8333708

P932

Q33804917-4D67926E-2BB6-447B-BBFC-013CDCADE9A7

P356

P1433

Scientific Reports

P1476

Highly stereoselective biosynt ...... ion of D-lactate dehydrogenase

@en

P2093

Binbin Sheng

http://www.w3.org/2001/XMLSchema#string

Cuiqing Ma

http://www.w3.org/2001/XMLSchema#string

Haiwei Zhang

http://www.w3.org/2001/XMLSchema#string

Tong Qin

http://www.w3.org/2001/XMLSchema#string

Zhaojuan Zheng

http://www.w3.org/2001/XMLSchema#string

P2860

Domain closure, substrate specificity and catalysis of D-lactate dehydrogenase from Lactobacillus bulgaricus

Crystal structure of a ternary complex of D-2-hydroxyisocaproate dehydrogenase from Lactobacillus casei, NAD+ and 2-oxoisocaproate at 1.9 A resolution

Efficient conversion of phenylpyruvic acid to phenyllactic acid by using whole cells of Bacillus coagulans SDM.

D-lactate dehydrogenase is a member of the D-isomer-specific 2-hydroxyacid dehydrogenase family. Cloning, sequencing, and expression in Escherichia coli of the D-lactate dehydrogenase gene of Lactobacillus plantarum.

Antimicrobial spectrum and target site of D-3-phenyllactic acid.

Utilization of molasses sugar for lactic acid production by Lactobacillus delbrueckii subsp. delbrueckii mutant Uc-3 in batch fermentation

Conversion of Lactobacillus pentosus D-lactate dehydrogenase to a D-hydroxyisocaproate dehydrogenase through a single amino acid replacement

A new chemo-enzymatic route to chiral 2-hydroxy-4-phenylbutyrates by combining lactonase-mediated resolution with hydrogenation over Pd/C.

Regeneration of nicotinamide coenzymes: principles and applications for the synthesis of chiral compounds.

Enantioselective oxidation of 2-hydroxy carboxylic acids by glycolate oxidase and catalase coexpressed in methylotrophic Pichia pastoris.

P2888

P304

3401

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/SREP03401

http://www.w3.org/2001/XMLSchema#string

P407

P478

3

http://www.w3.org/2001/XMLSchema#string

P50

P577

2013-12-02T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

259110244

http://www.w3.org/2001/XMLSchema#string

P6179

1000760134

http://www.w3.org/2001/XMLSchema#string

P698

24292439

http://www.w3.org/2001/XMLSchema#string

P921

stereoselectivity

P932

4070498

http://www.w3.org/2001/XMLSchema#string