生物
生物膜
伴侣(临床)
格罗尔
支原体
分枝杆菌
微生物学
突变体
生物化学
生物合成
霉酸
细菌
基因
结核分枝杆菌
遗传学
大肠杆菌
病理
医学
肺结核
作者
Anil K. Ojha,Mridula Anand,Apoorva Bhatt,Laurent Kremer,William R. Jacobs,Graham F. Hatfull
出处
期刊:Cell
[Cell Press]
日期:2005-12-01
卷期号:123 (5): 861-873
被引量:425
标识
DOI:10.1016/j.cell.2005.09.012
摘要
Mycobacteria are unusual in encoding two GroEL paralogs, GroEL1 and GroEL2. GroEL2 is essential—presumably providing the housekeeping chaperone functions—while groEL1 is nonessential, contains the attB site for phage Bxb1 integration, and encodes a putative chaperone with unusual structural features. Inactivation of the Mycobacterium smegmatis groEL1 gene by phage Bxb1 integration allows normal planktonic growth but prevents the formation of mature biofilms. GroEL1 modulates synthesis of mycolates—long-chain fatty acid components of the mycobacterial cell wall—specifically during biofilm formation and physically associates with KasA, a key component of the type II Fatty Acid Synthase involved in mycolic acid synthesis. Biofilm formation is associated with elevated synthesis of short-chain (C56–C68) fatty acids, and strains with altered mycolate profiles—including an InhA mutant resistant to the antituberculosis drug isoniazid and a strain overexpressing KasA—are defective in biofilm formation.
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