GroEL1: A dedicated chaperone involved in mycolic acid biosynthesis during biofilm formation in mycobacteria

被引:304
作者
Ojha, A
Anand, M
Bhatt, A
Kremer, L
Jacobs, WR
Hatfull, GF [1 ]
机构
[1] UIiv Pittsburgh, Dept Biol Sci, Pittsburgh Bacteriophage Inst, Pittsburgh, PA 15260 USA
[2] Albert Einstein Coll Med, Howard Hughes Med Inst, Bronx, NY 10461 USA
[3] Univ Montpellier 2, CNRS, UMR 5539, Lab Dynam Mol Interact Membranires, F-34095 Montpellier, France
关键词
D O I
10.1016/j.cell.2005.09.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 (C-56-C-68) 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.
引用
收藏
页码:861 / 873
页数:13
相关论文
共 71 条
[31]   Thiolactomycin and related analogues as novel anti-mycobacterial agents targeting KasA and KasB condensing enzymes in Mycobacterium tuberculosis [J].
Kremer, L ;
Douglas, JD ;
Baulard, AR ;
Morehouse, C ;
Guy, MR ;
Alland, D ;
Dover, LG ;
Lakey, JH ;
Jacobs, WR ;
Brennan, PJ ;
Minnikin, DE ;
Besra, GS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (22) :16857-16864
[32]   Inhibition of InhA activity, but not KasA activity, induces formation of a KasA-containing complex in mycobacteria [J].
Kremer, L ;
Dover, LG ;
Morbidoni, HR ;
Vilchèze, C ;
Maughan, WN ;
Baulard, A ;
Tu, SC ;
Honoré, N ;
Deretic, V ;
Sacchettini, JC ;
Locht, C ;
Jacobs, WR ;
Besra, GS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (23) :20547-20554
[33]   Temperature-induced changes in the cell-wall components of Mycobacterium thermoresistibile [J].
Kremer, L ;
Guérardel, Y ;
Gurcha, SS ;
Locht, C ;
Besra, GS .
MICROBIOLOGY-SGM, 2002, 148 :3145-3154
[34]   Mycolic acid biosynthesis and enzymic characterization of the β-ketoacyl-ACP synthase A-condensing enzyme from Mycobacterium tuberculosis [J].
Kremer, L ;
Dover, LG ;
Carrère, S ;
Nampoothiri, KM ;
Lesjean, S ;
Brown, AK ;
Brennan, PJ ;
Minnikin, DE ;
Locht, C ;
Besra, GS .
BIOCHEMICAL JOURNAL, 2002, 364 (02) :423-430
[35]  
Kremer L, 2000, MOLECULAR GENETICS OF MYCOBACTERIA, P173
[36]   Pseudo-outbreak of Mycobacterium chelonae and Methylobacterium mesophilicum caused by contamination of an automated endoscopy washer [J].
Kressel, AB ;
Kidd, F .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2001, 22 (07) :414-418
[37]   Accurate molecular mass determination of mycolic acids by MALDI-TOF mass spectrometry [J].
Laval, F ;
Lanéelle, MA ;
Déon, C ;
Monsarrat, B ;
Daffé, M .
ANALYTICAL CHEMISTRY, 2001, 73 (18) :4537-4544
[38]  
Lewis William M. Jr., 2000, Lakes Reservoirs Research and Management, V5, P35, DOI 10.1046/j.1440-1770.2000.00091.x
[39]   Mycobacterium tuberculosis chaperonin 60.1 is a more potent cytokine stimulator than chaperonin 60.2 (Hsp 65) and contains a CD14-binding domain [J].
Lewthwaite, JC ;
Coates, ARM ;
Tormay, P ;
Singh, M ;
Mascagni, P ;
Poole, S ;
Roberts, M ;
Sharp, L ;
Henderson, B .
INFECTION AND IMMUNITY, 2001, 69 (12) :7349-7355
[40]  
Maguire M, 2002, CELL STRESS CHAPERON, V7, P317, DOI 10.1379/1466-1268(2002)007<0317:CUISOC>2.0.CO