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Computational aided design of a halotolerant CMP kinase for enzymatic synthesis of cytidine triphosphate.
Wen, Qingshi; Zhang, Jie; Miao, Rongxin; Zhang, Bingyun; Yan, Ziyi; Ying, Hanjie; Wang, Junzhi.
Afiliación
  • Wen Q; Jiangsu Industrial Technology Research Institute, Nanjing Institute of White-Biotech Co.Ltd, Nanjing, China.
  • Zhang J; State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, No. 30, Puzhu South Road, Nanjing, 211816, China.
  • Miao R; National Engineering Technique Research Center for Biotechnology, Nanjing, 211816, China.
  • Zhang B; Jiangsu National Synergetic Innovation Center for Advanced Materials, Nanjing, China.
  • Yan Z; School of Life Sciences, Zhengzhou University, Zhengzhou, China.
  • Ying H; State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, No. 30, Puzhu South Road, Nanjing, 211816, China.
  • Wang J; National Engineering Technique Research Center for Biotechnology, Nanjing, 211816, China.
Bioprocess Biosyst Eng ; 46(4): 499-505, 2023 Apr.
Article en En | MEDLINE | ID: mdl-36800017
The current biocatalytic method of industrial Cytidine triphosphate (CTP) production suffers from reaction rate loss. It is caused by gradually increasing acetate salt concentration, which inhibits enzyme activities and decreases the final yield. This work gave a possible solution to this problem through computational aided design of CMP kinase (CMPK), an enzyme in the CTP production system, to increase its stability in solution with high acetate salt concentration. Enlightened by the features of natural halophilic enzymes, the basic and neutral surface residues were replaced with acidic amino acids. This protein design strategy effectively increased the activity of CMPK in the working condition (acetate concentration over 1200 mM). The halotolerant CMPK was applied in fed-batch production of CTP. The maximum titer was 201.4 ± 1.6 mM, and the productivity was 12.6 mM L-1 h-1, increased 26.4% and 27.8% from the process using wild-type CMPK, respectively.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nucleósido-Fosfato Quinasa Idioma: En Revista: Bioprocess Biosyst Eng Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nucleósido-Fosfato Quinasa Idioma: En Revista: Bioprocess Biosyst Eng Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania