枯草芽孢杆菌
生物
细胞质
重组DNA
分子生物学
计算生物学
细菌
生物化学
遗传学
基因
作者
Thu M.T. Dao,Dat D Truong,Lan NH Duong,Nhi N. Y. Nguyen,Hoang Duc Nguyen
出处
期刊:BioTechniques
[Future Science Ltd]
日期:2023-03-01
卷期号:74 (3): 123-129
被引量:14
标识
DOI:10.2144/btn-2022-0083
摘要
Bacillus subtilis is a critical host for producing recombinant proteins. However, the SDS-PAGE process, including the sample preparation steps, varies among B. subtilis-related studies, making it impossible to compare findings. Hence, this paper provides a simple guide to culture and collect B. subtilis cells through an OD600 measurement and a protocol for SDS-PAGE. These techniques were applied to check the expression of a BgaB, a reporter protein and LukF-PV, a potential vaccine candidate against S. aureus, in the cytoplasm of B. subtilis under the control of a strong promoter, Pgrac212. This protocol could be helpful for scientists in preparing samples and generating an SDS-PAGE experiment, as well as favoring the unification of research about protein expression in B. subtilis.
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