Advances in Enhanced Menaquinone-7 Production From Bacillus subtilis

被引:20
作者
Liao, Chaoyong [1 ]
Ayansola, Hammed [1 ]
Ma, Yanbo [2 ]
Ito, Koichi [3 ]
Guo, Yuming [1 ]
Zhang, Bingkun [1 ]
机构
[1] China Agr Univ, Coll Anim Sci & Technol, Dept Anim Nutr & Feed Sci, State Key Lab Anim Nutr, Beijing, Peoples R China
[2] Henan Univ Sci & Technol, Coll Anim Sci & Technol, Dept Anim Physiol, Henan Int Joint Lab Anim Welf & Hlth Breeding, Luoyang, Peoples R China
[3] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Food & Physiol Models, Ibaraki, Japan
关键词
Bacillus subtilis; menaquinone-7; synthetic biology; chassis cells; CRISPR interference; CRISPR activation; IRON-OXIDE NANOPARTICLES; VITAMIN-K; FUNCTIONAL-ANALYSIS; GROWTH-PARAMETERS; BIOFILM; GENOME; BIOSYNTHESIS; OPTIMIZATION; PATHWAY; FERMENTATION;
D O I
10.3389/fbioe.2021.695526
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The production of nutraceutical compounds through biosynthetic approaches has received considerable attention in recent years. For example, Menaquinone-7 (MK-7), a sub-type of Vitamin K2, biosynthesized from Bacillus subtilis (B. subtilis), proved to be more efficiently produced than the conventional chemical synthesis techniques. This is possible due to the development of B. subtilis as a chassis cell during the biosynthesis stages. Hence, it is imperative to provide insights on the B. subtilis membrane permeability modifications, biofilm reactors, and fermentation optimization as advanced techniques relevant to MK-7 production. Although the traditional gene-editing method of homologous recombination improves the biosynthetic pathway, CRISPR-Cas9 could potentially resolve the drawbacks of traditional genome editing techniques. For these reasons, future studies should explore the applications of CRISPRi (CRISPR interference) and CRISPRa (CRISPR activation) system gene-editing tools in the MK-7 anabolism pathway.
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页数:13
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