In silico screening and validation of different dehydrogenases to produce 2,3-butanediol in Bacillus subtilis

被引:2
|
作者
Asolkar, Sailee Sanjay [1 ,2 ]
Anju, M. [3 ]
Kumar, Ravindra [3 ]
Deshmukh, Apoorva [2 ]
Ghosalkar, Anand [1 ,2 ]
Kumbhar, Pramod [1 ,2 ]
机构
[1] Savitribai Phule Pune Univ, Dept Technol, Pune 411007, Maharashtra, India
[2] Div Praj Ind Ltd, Praj Matrix R&D Ctr, Pune 412115, India
[3] Natl Inst Technol Calicut, Dept Biosci & Engn, Kozhikode 673601, Kerala, India
关键词
2,3-butanediol; Enzymes; Heterologous expression; Bacillus subtilis; In silico; Docking; MESO-2,3-BUTANEDIOL DEHYDROGENASE; SACCHAROMYCES-CEREVISIAE; BDHA-GENE; EXPRESSION; CLONING; INTEGRATION; BINDING; ZINC;
D O I
10.1007/s12257-024-00053-1
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
Bacillus subtilis is a natural producer of 2,3-butanediol (2,3-BDO) and has acquired "Generally Regarded as Safe" status. It is reported to produce 2,3-BDO from synthetic sugars as well as complex and economic sugar sources such as molasses. However, the rate-limiting step in the formation of 2,3-BDO is its conversion from acetoin to 2,3-BDO by the enzyme butanediol dehydrogenase (2,3-BDH). Such 2,3-BDHs were screened based on higher affinity (lower K-m) towards acetoin as substrate. The in silico docking studies were conducted for further validation, and they showed a high interaction profile for the PpBDH protein towards acetoin. Heterologous expression of these genes was studied in engineered Bacillus subtilis (BS1A1). In this study, it was seen that 2,3-BDH from Paenibacillus polymyxa ZJ-9 was reported to have higher enzyme activity levels, and in the fermentation studies, it was seen that the ratio of 2,3-BDO to acetoin was increased by 80.25%. The insights encourage further bioprocess optimization for increasing the fermentative production of 2,3-BDO. Our results provide a potential strategy to avoid the back conversion of 2,3-BDO to acetoin in an engineered Bacillus system.
引用
收藏
页码:271 / 290
页数:20
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