Literature DB >> 25326062

Development of an efficient process intensification strategy for enhancing Pfu DNA polymerase production in recombinant Escherichia coli.

Jian-Hua Hu1, Feng Wang, Chun-Zhao Liu.   

Abstract

An efficient induction strategy that consisted of multiple additions of small doses of isopropyl-β-D-thiogalactopyranoside (IPTG) in the early cell growth phase was developed for enhancing Pfu DNA polymerase production in Escherichia coli. In comparison to the most commonly used method of a single induction of 1 mM IPTG, the promising induction strategy resulted in an increase in the Pfu activity of 13.5% in shake flasks, while simultaneously decreasing the dose of IPTG by nearly half. An analysis of the intracellular IPTG concentrations indicated that the cells need to maintain an optimum intracellular IPTG concentration after 6 h for efficient Pfu DNA polymerase production. A significant increase in the Pfu DNA polymerase activity of 31.5% under the controlled dissolved oxygen concentration of 30% in a 5 L fermentor was achieved using the multiple IPTG induction strategy in comparison with the single IPTG induction. The induction strategy using multiple inputs of IPTG also avoided over accumulation of IPTG and reduced the cost of Pfu DNA polymerase production.

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Year:  2014        PMID: 25326062     DOI: 10.1007/s00449-014-1304-4

Source DB:  PubMed          Journal:  Bioprocess Biosyst Eng        ISSN: 1615-7591            Impact factor:   3.210


  6 in total

1.  Construction, Expression, and Characterization of Recombinant Pfu DNA Polymerase in Escherichia coli.

Authors:  Wenjun Zheng; Qingsong Wang; Qun Bi
Journal:  Protein J       Date:  2016-04       Impact factor: 2.371

2.  Characterization of Recombinant Thermococcus kodakaraensis (KOD) DNA Polymerases Produced Using Silkworm-Baculovirus Expression Vector System.

Authors:  Mami Yamashita; Jian Xu; Daisuke Morokuma; Kazuma Hirata; Masato Hino; Hiroaki Mon; Masateru Takahashi; Samir M Hamdan; Kosuke Sakashita; Kazuhiro Iiyama; Yutaka Banno; Takahiro Kusakabe; Jae Man Lee
Journal:  Mol Biotechnol       Date:  2017-06       Impact factor: 2.695

3.  Identification of Optimal Expression Parameters and Purification of a Codon-Optimized Human GLIS1 Transcription Factor from Escherichia coli.

Authors:  Chandrima Dey; Vishalini Venkatesan; Rajkumar P Thummer
Journal:  Mol Biotechnol       Date:  2021-09-15       Impact factor: 2.695

4.  A simple method for in-house Pfu DNA polymerase purification for high-fidelity PCR amplification.

Authors:  Prabu Siva Sankar; Marimuthu Citartan; Aminah Ahmed Siti; Boris V Skryabin; Timofey S Rozhdestvensky; Goot Heah Khor; Thean Hock Tang
Journal:  Iran J Microbiol       Date:  2019-04

5.  Levulinic Acid-Inducible and Tunable Gene Expression System for Methylorubrum extorquens.

Authors:  Chandran Sathesh-Prabu; Young Shin Ryu; Sung Kuk Lee
Journal:  Front Bioeng Biotechnol       Date:  2021-12-15

6.  Process study of ceramic membrane-coupled mixed-cell fermentation for the production of adenine.

Authors:  Pengjie Sun; Changgeng Li; Yu Gong; Jinduo Wang; Qingyang Xu
Journal:  Front Bioeng Biotechnol       Date:  2022-08-10
  6 in total

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