Back to Search Start Over

iTRAQ analysis reveals the effect of gabD and sucA gene knockouts on lysine metabolism and crystal protein formation in Bacillus thuringiensis.

Authors :
Yi, Zixian
Zhang, Tong
Xie, Junyan
Zhu, Zirong
Luo, Sisi
Zhou, Kexuan
Zhou, Pengji
Chen, Wenhui
Zhao, Xiaoli
Sun, Yunjun
Xia, Liqiu
Ding, Xuezhi
Source :
Environmental Microbiology. Apr2021, Vol. 23 Issue 4, p2230-2243. 14p.
Publication Year :
2021

Abstract

Summary: Lysine metabolism plays an important role in the formation of the insecticidal crystal proteins of Bacillus thuringiensis (Bt). The genes lam, gabD and sucA encode three key enzymes of the lysine metabolic pathway in Bt4.0718. The lam gene mainly affects the cell growth at stable period, negligibly affected sporulation and insecticidal crystal protein (ICP) production. While, the deletion mutant strains of the gabD and sucA genes showed that the growth, sporulation and crystal protein formation were inhibited, cells became slender, and insecticidal activity was significantly reduced. iTRAQ proteomics and qRT‐PCR used to analyse the differentially expressed protein (DEP) between the two mutant strains and the wild type strain. The functions of DEPs were visualized and statistically classified, which affect bacterial growth and metabolism by regulating biological metabolism pathways: the major carbon metabolism pathways, amino acid metabolism, oxidative phosphorylation pathways, nucleic acid metabolism, fatty acid synthesis and peptidoglycan synthesis. The gabD and sucA genes in lysine metabolic pathway are closely related to the sporulation and crystal proteins formation. The effects of DEPs and functional genes on basic cellular metabolic pathways were studied to provide new strategies for the construction of highly virulent insecticidal strains, the targeted transformation of functional genes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14622912
Volume :
23
Issue :
4
Database :
Academic Search Index
Journal :
Environmental Microbiology
Publication Type :
Academic Journal
Accession number :
149927206
Full Text :
https://doi.org/10.1111/1462-2920.15359