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Significantly enhancing recombinant alkaline amylase production in Bacillus subtilis by integration of a novel mutagenesis-screening strategy with systems-level fermentation optimization
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Alkaline amylase has significant potential for applications in the textile, paper and detergent industries, however, low yield of which cannot meet the requirement of industrial application. In this work, a novel ARTP mutagenesis-screening method and fermentation optimization strategies were used to significantly improve the expression level of recombinant alkaline amylase in B. subtilis 168. The activity of alkaline amylase in mutant B. subtilis 168 mut-16# strain was 1.34-fold greater than that in the wild-type, and the highest specific production rate was improved from 1.31 U/(mg·h) in the wild-type strain to 1.57 U/(mg·h) in the mutant strain. Meanwhile, the growth of B. subtilis was significantly enhanced by ARTP mutagenesis. When the agitation speed was 550 rpm, the highest activity of recombinant alkaline amylase was 1.16- and 1.25-fold of the activities at 450 and 650 rpm, respectively. When the concentration of soluble starch and soy peptone in the initial fermentation medium was doubled, alkaline amylase activity was increased 1.29-fold. Feeding hydrolyzed starch and soy peptone mixture or glucose significantly improved cell growth, but inhibited the alkaline amylase production in B. subtilis 168 mut-16#. The highest alkaline amylase activity by feeding hydrolyzed starch reached 591.4 U/mL, which was 1.51-fold the activity by feeding hydrolyzed starch and soy peptone mixture. Single pulse feeding-based batch feeding at 10 h favored the production of alkaline amylase in B. subtilis 168 mut-16#. The results indicated that this novel ARTP mutagenesis-screening method could significantly improve the yield of recombinant proteins in B. subtilis . Meanwhile, fermentation optimization strategies efficiently promoted expression of recombinant alkaline amylase in B. subtilis 168 mut-16#. These findings have great potential for facilitating the industrial-scale production of alkaline amylase and other enzymes, using B. subtilis cultures as microbial cell factories.
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“The effective use of soya peptone or soya protein hydrolysate as nitrogen sources by some strains of B. subtilis has been reported, where high cell density biomass production was a prerequisite for the synthesis of certain secondary metabolites and industrially important enzymes [21-23].”
From Optimization of Bacillus subtilis PW12 biomass production using RSM: a preliminary study towards single-cell protein production for aquaculture (2024) · cites this paper as [23]
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“The biomass yield obtained in this investigation was similar to that reported in the study of Ma et al. [23] in which a fed batch fermentation experiment with a mutant strain of B. subtilis 168 mut-16# was conducted. Feeding of soya peptone and hydrolyzed starch to the medium increased the dry cell weight of the bacteria, and the highest dry cell weight obtained was 14.3 g/L which”
From Optimization of Bacillus subtilis PW12 biomass production using RSM: a preliminary study towards single-cell protein production for aquaculture (2024) · cites this paper as [23]
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Cited by
Gracious, M., & Nandakumar, S. (2024) · Journal of Applied Biology & Biotechnology · doi:10.7324/jabb.2024.177031 · Cited by 2
“The biomass yield obtained in this investigation was similar to that reported in the study of Ma et al. [23] in which a fed batch fermentation experiment with a mutant strain of B. subtilis 168 mut-16# was conducted.”
Metadata
- Authors
- Ma, Y., Shen, W., Chen, X., Liu, L., Zhou, Z., Xu, F., & Yang, H.
- Affiliations
- Jiangnan University (CN)
- Corresponding author
- Yang, Haiquan
- Venue
- Journal of Biological Engineering
- Published
- 2016-10-17
- Volume
- 10
- Issue
- 1
- Pages
- 13-13
- ISSN
- 1754-1611 (ISSN-L)
- PMC
- PMC5067897
- OpenAlex
- W2533170373
- Cited by
- 36
- References
- 1
- Citations by year
- 2025: 3 · 2024: 1 · 2023: 1 · 2022: 6 · 2021: 4 · 2020: 6 · 2019: 7 · 2018: 5 · 2017: 3
- FWCI
- 4.37
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Journal of Biological Engineering (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- 863 Program (2014AA021304)
- Natural Science Foundation of Jiangsu Province (BK20140152)
- National Natural Science Foundation of China (CN) (21406089)
- the Open Project Program of the Key Laboratory of Industrial Biotechnology, Ministry of Education, China (KLIB-KF201509)
- 111 Project (111-2-06)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Enzyme Production and Characterization
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- Bacillus subtilis, recombinant protein expression, fermentation optimization, soy peptone, stirring speed, enzyme production, microbial cell factories
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- Ma, Y., Shen, W., Chen, X., Liu, L., Zhou, Z., Xu, F., & Yang, H. (2016). Significantly enhancing recombinant alkaline amylase production in Bacillus subtilis by integration of a novel mutagenesis-screening strategy with systems-level fermentation optimization. Journal of Biological Engineering. https://doi.org/10.1186/s13036-016-0035-2