An operon for a putative ATP-binding cassette transport system involved in acetoin utilization of Bacillus subtilis

被引:48
作者
Yoshida, KI
Fujita, Y
Ehrlich, SD
机构
[1] Fukuyama Univ, Dept Biotechnol, Hiroshima 7290292, Japan
[2] INRA, F-78352 Jouy En Josas, France
关键词
D O I
10.1128/JB.182.19.5454-5461.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The ytrABCDEF operon of Bacillus subtilis was deduced to encode a putative ATP-binding cassette (ABC) transport system, YtrB and YtrE could be the ABC subunits, and YtrC and YtrD are highly hydrophobic and could form a channel through the cell membrane, while YtrF could be a periplasmic lipoprotein for substrate binding. Expression of the operon was examined in cells grown in a minimal medium. The results indicate that the expression was induced only early in the stationary phase. The six ytr genes form a single operon, transcribed from a putative sigma(A)-dependent promoter present upstream of ytrA. YtrA, which possesses a helix-turn-helix. motif of the GntR family, acts probably as a repressor and regulates its own transcription. Inactivation of the operon led to a decrease in maximum cell yield and less-efficient sporulation, suggesting its involvement in the growth in stationary phase and sporulation. It is known that B. subtilis produces acetoin as an external carbon storage compound and then reuses it later during stationary phase and sporulation, When either the entire ytr operon or its last gene, ytrF, was inactivated, the production of acetoin was not affected, but the reuse of acetoin became less efficient. We suggest that the Ytr transport system plays a role in acetoin utilization during stationary phase and sporulation.
引用
收藏
页码:5454 / 5461
页数:8
相关论文
共 29 条
[1]   BACTERIAL PERIPLASMIC PERMEASES BELONG TO A FAMILY OF TRANSPORT PROTEINS OPERATING FROM ESCHERICHIA-COLI TO HUMAN - TRAFFIC ATPASES [J].
AMES, GF ;
MIMURA, CS ;
SHYAMALA, V .
FEMS MICROBIOLOGY LETTERS, 1990, 75 (04) :429-446
[2]   ABC TRANSPORTERS - BACTERIAL EXPORTERS [J].
FATH, MJ ;
KOLTER, R .
MICROBIOLOGICAL REVIEWS, 1993, 57 (04) :995-1017
[3]   Identification and expression of the Bacillus subtilis fructose-1,6-bisphosphatase gene (fbp) [J].
Fujita, Y ;
Yoshida, KI ;
Miwa, Y ;
Yanai, N ;
Nagakawa, E ;
Kasahara, Y .
JOURNAL OF BACTERIOLOGY, 1998, 180 (16) :4309-4313
[4]   IDENTIFICATION OF GENES INVOLVED IN UTILIZATION OF ACETATE AND ACETOIN IN BACILLUS-SUBTILIS [J].
GRUNDY, FJ ;
WATERS, DA ;
TAKOVA, TY ;
HENKIN, TM .
MOLECULAR MICROBIOLOGY, 1993, 10 (02) :259-271
[5]   A NEW FAMILY OF BACTERIAL REGULATORY PROTEINS [J].
HAYDON, DJ ;
GUEST, JR .
FEMS MICROBIOLOGY LETTERS, 1991, 79 (2-3) :291-296
[6]   Biochemical and molecular characterization of the Bacillus subtilis acetoin catabolic pathway [J].
Huang, M ;
Oppermann-Sanio, FB ;
Steinbüchel, A .
JOURNAL OF BACTERIOLOGY, 1999, 181 (12) :3837-3841
[7]  
KERPPOLA RE, 1991, J BIOL CHEM, V266, P9857
[8]   The complete genome sequence of the Gram-positive bacterium Bacillus subtilis [J].
Kunst, F ;
Ogasawara, N ;
Moszer, I ;
Albertini, AM ;
Alloni, G ;
Azevedo, V ;
Bertero, MG ;
Bessieres, P ;
Bolotin, A ;
Borchert, S ;
Borriss, R ;
Boursier, L ;
Brans, A ;
Braun, M ;
Brignell, SC ;
Bron, S ;
Brouillet, S ;
Bruschi, CV ;
Caldwell, B ;
Capuano, V ;
Carter, NM ;
Choi, SK ;
Codani, JJ ;
Connerton, IF ;
Cummings, NJ ;
Daniel, RA ;
Denizot, F ;
Devine, KM ;
Dusterhoft, A ;
Ehrlich, SD ;
Emmerson, PT ;
Entian, KD ;
Errington, J ;
Fabret, C ;
Ferrari, E ;
Foulger, D ;
Fritz, C ;
Fujita, M ;
Fujita, Y ;
Fuma, S ;
Galizzi, A ;
Galleron, N ;
Ghim, SY ;
Glaser, P ;
Goffeau, A ;
Golightly, EJ ;
Grandi, G ;
Guiseppi, G ;
Guy, BJ ;
Haga, K .
NATURE, 1997, 390 (6657) :249-256
[9]   RELATIONS BETWEEN CATABOLITE REPRESSION AND SPORULATION IN BACILLUS-SUBTILIS [J].
LOPEZ, JM ;
THOMS, B .
ARCHIVES OF MICROBIOLOGY, 1976, 109 (1-2) :181-186
[10]  
MIWA Y, 1988, J BIOL CHEM, V263, P13252