| Literature DB >> 33651593 |
Xiaoqiang Yin1,2, Yangyang Li1,2, Jingwen Zhou1,2,3, Shengqi Rao4, Guocheng Du2,5, Jian Chen1,2,3, Song Liu1,2.
Abstract
Streptomyces transglutaminase (TGase) is widely used to improve food texture properties. In this study, random mutagenesis and site-directed genetic modification were used to improve the production of TGase in Streptomyces mobaraensis. First, S. mobaraensis DSM40587 (smWT) was subjected to atmospheric and room-temperature plasma mutagenesis, and then a mutant (smY2019) with a 5.5-fold increase in TGase yield was screened from approximately 3000 × 25 (round) mutants. Compared to smWT, smY2019 exhibits a 3.2-fold higher TGase mRNA level and two site mutations within the -10 region of the TGase promoter. The recombinant expression analysis in the TGase-deficient S. mobaraensis suggests that the mutated TGase promoter is more robust than the wild-type one. Finally, we integrated two additional TGase expression cassettes into the smY2019 genome, yielding the recombinant strain smY2019-3C with a 103% increase in TGase production compared to smY2019. The smY2019-3C strain with 40 U/mL of TGase yield could be a suitable candidate for the industrial production of TGase.Entities:
Keywords: ARTP; Streptomyces mobaraensis; expression cassette; gene copy; promoter; transglutaminase
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Year: 2021 PMID: 33651593 DOI: 10.1021/acs.jafc.1c00645
Source DB: PubMed Journal: J Agric Food Chem ISSN: 0021-8561 Impact factor: 5.279