A kind of l-threonine aldolase mutant, gene and method for preparing l-syn-p-thymphenylphenylserine

A methylsulfonyl phenylserine and threonine aldolase technology, which is applied in the field of enzyme engineering, can solve the problems of only 50% theoretical yield, difficult to apply invalid enantiomers, low atom utilization rate, etc., and achieves the optical purity of products. High, high atomic utilization, low pollution effect

Active Publication Date: 2021-05-14
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This process mainly has the following disadvantages: the theoretical yield is only 50%, the invalid enantiomer is difficult to apply mechanically, and the process is relatively complicated
This process has the following disadvantages: the production process is complicated, the utilization rate of atoms is not high, the theoretical yield can only reach 50%, and the problem of copper salt environmental pollution will also occur
Therefore, there is no research report on the direct application of L-threonine aldolase to synthesize high-chiral purity L-syn-p-thiamphenicol phenylserine

Method used

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  • A kind of l-threonine aldolase mutant, gene and method for preparing l-syn-p-thymphenylphenylserine
  • A kind of l-threonine aldolase mutant, gene and method for preparing l-syn-p-thymphenylphenylserine
  • A kind of l-threonine aldolase mutant, gene and method for preparing l-syn-p-thymphenylphenylserine

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] Embodiment 1: Construction of wild enzyme engineering bacteria

[0050] Enter keywords such as threoninealdolase in the National Coalition Building Institute (NCBI) database to search and select the amino acid sequence WP_015261381.1 (derived from Desulfitobacterium dichloroeliminans (DdLTA)) and SIS82838.1 (derived from Chryseobacterium chaponense (CcLTA)), WP_016204489.1 (derived from Bacillus nealsonii (BnLTA)), WP_023973138.1 (derived from Clostridium beijerinckii (CbLTA)), WP_077361571.1 (derived from Clostridium saccharoperbutylacetonicum (CsLTA)), 919 (derived from WP4969 in Cellulosilyticum sp.I15G10I2(CpLTA)). The six amino acid sequences were converted into nucleotide sequences according to the codon preference of Escherichia coli (the nucleotide sequences are shown in SEQ ID No. 1-6). The six nucleotide sequences were fully synthesized by chemical method (Anhui General Biology), and integrated between the multiple cloning sites BamH I and Hind III of the exp...

Embodiment 2

[0051] Embodiment 2: the construction of mutant enzyme

[0052] 1. Activation of Engineering Bacteria and Plasmid Extraction

[0053] All engineering bacteria (constructed and obtained in Example 1) were activated and cultivated using LB medium, and the formula was: peptone 10g / L, yeast powder 5g / L, NaCl 10g / L, dissolved in deionized water and then constant volume, 115 Sterilize at ℃ for 30min, and set aside. The solid medium is LB medium with 2% agar added.

[0054] The preserved engineered bacteria glycerol tube was inserted into a test tube containing 10 mL of LB medium, and cultured at 37°C and 200 rpm for 12 hours. After obtaining the cultured cells, plasmid extraction was carried out according to the operating instructions of the Axygen plasmid extraction kit. The resulting plasmid can be directly used for point mutation or stored at -20°C for a long time.

[0055] 2. Gene site-directed mutation

[0056] The gene mutation adopts the method of whole plasmid PCR to ob...

Embodiment 3

[0071] Embodiment 3: the preparation of the culture of thalline and crude enzyme liquid

[0072] 1. Bacteria culture

[0073] Composition of LB liquid medium: peptone 10g / L, yeast powder 5g / L, NaCl 10g / L, dissolved in deionized water and then constant volume, sterilized at 115°C for 30min, ready for use.

[0074] After the engineering bacteria containing the L-threonine aldolase gene were activated by streaking on a plate, a single colony was picked and inoculated into 5 mL LB liquid medium containing 50 μg / mL kanamycin, and cultured with shaking at 37°C for 12 hours. Transfer 2% of the inoculum into 50 mL of fresh LB liquid medium also containing 50 μg / ml Kan, culture with shaking at 37 °C until the OD600 reaches about 0.6, add IPTG to a final concentration of 0.5 mM, and induce culture at 28 °C 10h. After the cultivation, the culture solution was centrifuged at 10,000 rpm for 10 min, the supernatant was discarded, and the bacterial cells were collected, and stored in a -80...

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Abstract

The invention discloses an L-threonine aldolase mutant, a gene and a method for preparing L-syn-p-methylsulfonylphenylserine. The L-threonine aldolase mutant is obtained by mutation of wild-type L-threonine aldolase, and can use glycine and p-methylsulfonylbenzaldehyde as substrates and pyridoxal phosphate as coenzyme to catalyze condensation The reaction produces L-syn-p-methylsulfonylphenylserine. Using the L-threonine aldolase mutant of the present invention to produce L-syn-p-methylsulfonylphenylserine has the following advantages: 1. the production process is simple and the reaction conditions are mild; 2. the selection of L-threonine aldolase High performance, high optical purity of the product, no need for splitting; 3. High atomic utilization rate, theoretically up to 100%; 4. Environmental protection in the production process, less pollution, in line with the concept of green chemistry; 5. Simple product separation and purification.

Description

technical field [0001] The invention relates to the technical field of enzyme engineering, in particular to an L-threonine aldolase mutant, a gene and a method for preparing L-syn-p-thymphenylphenylserine. Background technique [0002] L-syn-p-thymphenylphenylserine is an important pharmaceutical intermediate used in the synthesis of various antibiotics. P-thiamphenicyl phenylserine has two chiral centers and has four isomers, namely: L-syn-p-thiamphenicyl phenylserine, L-anti-p-thiamphenicyl phenylserine, D-syn-p Thiysulfonyl phenylserine, D-anti-p-thysulfonyl phenylserine ( figure 1 ). [0003] At present, there are mainly two production methods for L-syn-p-thymphenylphenylserine. One is chemical synthesis, using copper sulfate as a catalyst, utilizing the complexation of metal ions, and selectively reacting p-thiamphenicol benzaldehyde and glycine to generate two cis products: L-syn-p-thiamphenicyl phenylserine Copper and D-syn-copper p-thiamphenicyl phenylserine, the...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N9/88C12N15/60C12N15/70C12N1/21C12P13/04C12R1/19
CPCC12N9/88C12N15/70C12P13/04C12Y401/02005
Inventor 吴坚平郑文隆陈开通徐刚杨立荣
Owner ZHEJIANG UNIV
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