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Carbonyl reductase gene, codase, vector, strain and application of gene

A technology of carbonyl reductase and reductase, which is applied in the direction of oxidoreductase, application, genetic engineering, etc., can solve the problem of low catalytic efficiency

Active Publication Date: 2015-11-11
ZHEJIANG UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The currently reported catalytic asymmetric reduction of tert-butyl (S)-6-chloro-5-hydroxy-3-carbonylhexanoate to tert-butyl 6-chloro-(3R,5S)-dihydroxyhexanoate with high stereoselectivity The strains have Lactobacilluskefir and SaccharomycescerevisiaeCGMCCNo.2233, etc., but the catalytic efficiency is low

Method used

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  • Carbonyl reductase gene, codase, vector, strain and application of gene
  • Carbonyl reductase gene, codase, vector, strain and application of gene
  • Carbonyl reductase gene, codase, vector, strain and application of gene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0050] Example 1 Acquisition of Rhodosporidium toruloides (Rhodosporidium toruloides) ZJB2014212

[0051] The present invention takes soil samples from Zhejiang, Hubei, Anhui, Jiangsu and other places, and takes 30 soil samples altogether. The specific method of screening: Weigh 5g of soil sample, add 50mL of sterile water to make soil suspension, take 1.0mL of supernatant, add it to the screening medium, shake and cultivate at 30°C, 150rpm / min on a shaker for 48h. Take the culture solution for gradient dilution, take 10 -5 、10 -6 and 10 -7 Gradient dilutions of the above samples were spread on LB solid medium, and cultured in a constant temperature incubator at 30°C for 48 hours. The grown single colony was picked and inoculated into the liquid fermentation medium for cultivation. Cultivate on a shaker at 30°C for 48 hours, collect the cells by centrifugation, and wash with phosphate buffer. The cells are used for transformation, and the transformation conditions are as ...

Embodiment 2

[0062] Example 2: Amplification of the carbonyl reductase gene rtscr9

[0063]According to the whole genome sequencing information of Rhodosporidium toruloides (Rhodosporidium toruloides) ZJB2014212, carbonyl reductases with potential catalytic activity were excavated, one of which has the ability to catalyze N,N-dimethyl-3-keto-3-(2-thienyl)propane The enzyme with the function of generating (S)-N,N-bismethyl-3-hydroxyl-3-(2-thienyl)propionamide from amide hydrochloride is the carbonyl reductase RtSCR9 involved in the present invention.

[0064] Using Ambion's The reagents were used to extract the total mRNA of Rhodosporidium toruloides ZJB2014212 cells. 1 mg mRNA was taken as a template, and cDNA was synthesized by reverse transcription using the ReverTraAceqPCRRT kit (ToYoBo, Japan). Using the cDNA as a template, PCR amplification was performed under the action of primer 1 (ATGTCTTCGCCTACTCCCAACGTC) and primer 2 (CTACCATGGCAAGAACGTCCCGTC). PCR reaction system (total volu...

Embodiment 3

[0067] Embodiment 3: Construction of recombinant Escherichia coli BL21(DE3) / pET28a-rtscr9

[0068] Design expression primer 3 ( catatg TCTTCGCCTACTCCCAACGTC), primer 4 ( aagctt CTACCATGGCAAGAACGTCCCGTC), and NdeI and HindIII restriction enzyme sites (underlined) were introduced into primer 3 and primer 4, respectively. Under the priming of primer 3 and primer 4, utilize high-fidelity PfuDNA polymerase to amplify, obtain the carbonyl reductase gene sequence (its nucleotide sequence is as shown in SEQIDNO: 1) of length 759bp, use NdeI and HindIII after sequencing The amplified fragment was treated with a restriction endonuclease (TaKaRa), and the fragment was ligated with the commercial vector pET28a (Invitrogen) treated with the same restriction endonuclease using T4 DNA ligase (TaKaRa) to construct an expression vector pET28a-rtscr9. The constructed expression vector pET28a-rtscr9 was transformed into Escherichia coli BL21(DE3) (Invitrogen), spread on LB plates containing...

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Abstract

The invention discloses a carbonyl reductase derived from Rhodosporidium toruloides ZJB14212, a gene, a vector, a strain and an application of the carbonyl reductase in the preparation of chiral drug intermediates. The above carbonyl reductase can biologically catalyze preparation of highly optically pure (S)-N,N-dimethyl-3-hydroxy-3-(2-thienyl)propionamide, (S)-N-methyl-3-hydroxy-3-(2-thienyl)propionamide, (R)-3-chloro-1-(2-thienyl)1-propanol, ethyl (S)-3-hydroxy-3-(2-thienyl)propanoate, (S)-3-hydroxy-3-(2-thienyl)propionitrile, tert-butyl 6-chloro-(3R,5S)-dihydroxyhexanoate, (4S)-3-[(5S)-5-(4-fluorophenyl)-5-hydroxyvaleryl]-4-phenyl-1,3-oxazolidine-2-one and methyl [S-(E)]-2-[3-[3-[2-(7-chloro-2-quinolyl)vinyl]phenyl]-3-hydroxypropyl]benzoate.

Description

(1) Technical field [0001] The invention relates to a carbonyl reductase gene extracted from Rhodosporidium toruloides ZJB2014212, encoding enzyme, carrier, strain and application. (2) Background technology [0002] Stereoselective carbonyl reductase (Specific Carbonyl Reductase, SCR; Ketoreductase, KRED, EC1.1.1.x) is a class of enzymes that can catalyze a bidirectional reversible redox reaction between alcohols and aldehydes / ketones, and requires the coenzyme NAD(H) (tobacco amide adenine dinucleotide) or NADP(H) (nicotinamide adenine dinucleotide phosphate) as hydrogen transporter. NADH and NADPH participate in the reduction reaction as electron donors, and NAD and NADP participate in the oxidation reaction as electron acceptors. At present, stereoselective carbonyl reductases are mainly distributed in three superfamilies: Short-Chain Dehydrogenase / Reductases (SDRs), Medium-Chain Dehydrogenases / Reductases (MDRs) And aldehyde ketone reductase (Aldo-KetoReductases, AKRs)....

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/53C12N9/04C12N15/70C12N1/21C12P13/02C12P7/62C12P13/00C12P17/14C12N1/16C12R1/645
Inventor 柳志强郑裕国陈翔林超平王亚军吴林姚丹凯余道褔胡忠梁董思川沈寅初
Owner ZHEJIANG UNIV OF TECH
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