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High-level production of short branched-chain fatty acids from waste materials by genetically modified Bacillus licheniformis

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成果类型:
期刊论文
作者:
Shi, Jiao;Zhan, Yangyang;Zhou, Mengling;He, Min;Wang, Qin;...
通讯作者:
Chen, Shouwen
作者机构:
[Zhan, Yangyang; He, Min; Shi, Jiao; Chen, Shouwen; Zhou, Mengling; Wang, Qin] Hubei Univ, Coll Life Sci, Hubei Collaborat Innovat Ctr Green Transformat Bi, Environm Microbial Technol Ctr Hubei Prov, Wuhan 430062, Hubei, Peoples R China.
[Li, Xin] Wuhan Polytech Univ, Coll Biol & Pharmaceut Engn, Wuhan 430023, Hubei, Peoples R China.
[Wen, Zhiyou] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Hubei, Peoples R China.
[Wen, Zhiyou] Iowa State Univ, Dept Food Sci & Human Nutr, Ames, IA 50011 USA.
[Chen, Shouwen] 368 Youyi Ave, Wuhan 430062, Hubei, Peoples R China.
通讯机构:
[Chen, Shouwen] 3
368 Youyi Ave, Wuhan 430062, Hubei, Peoples R China.
语种:
英文
关键词:
Bacillus licheniformis;Bean dreg;Crude glycerol;Metabolic engineering;Process optimization;Short branched-chain fatty acids
期刊:
Bioresource Technology
ISSN:
0960-8524
年:
2019
卷:
271
页码:
325-331
基金类别:
The total RNA was extracted by according to the previous report (Li et al., 2012b). Before RNA extraction, all the samples were filtrated through filter paper to remove bean dreg residue. The HiScript®II Q RT SuperMix for qPCR (+gDNA wiper) (Vazyme, China) was used for DNA digestion and cDNA synthesis following the manufacturer’s instructions. The real-time PCR was performed by using iTaq™ Universal SYBR® Green Supermix (BIO-RAD, USA) by the manufacturer. The 16S rRNA gene was served as the
机构署名:
本校为其他机构
院系归属:
生命科学与技术学院
摘要:
Short branched-chain fatty acids (SBCFAs) are multi-functional platform chemicals used in many fields. Currently, SBCFAs are produced mainly by chemical synthesis, which is high cost and lead to environmental pollution. The aim of this study was to achieve high-level production of SBCFAs from waste materials, bean dreg and crude glycerol. The Bacillus licheniformis DWc9n∗ was genetically modified by overexpression of SBCFAs synthesis genes via replacement of native promoter of bkd operon, the mutant strain DWc9n∗-PbacA produced 4.68 g/L of SB...

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