Regulated expression of HPrK/P does not affect carbon catabolite repression of the xyn operon and of rocG in Bacillus subtilis

被引:4
作者
Bertram, R [1 ]
Wünsche, A [1 ]
Sprehe, M [1 ]
Hillen, W [1 ]
机构
[1] Univ Erlangen Nurnberg, Inst Biol, Lehrstuhl Mikrobiol, D-91058 Erlangen, Germany
关键词
gene regulation; carbon catabolism; tetracycline;
D O I
10.1111/j.1574-6968.2006.00260.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HPr kinase/phosphorylase (HPrK/P), a central metabolic regulator in many Gram-positive bacteria, reversibly phosphorylates HPr and Crh, thus controlling their activities as effectors of CcpA predominantly in carbon catabolite repression (CCR). We have placed the constitutively expressed hprK in its native chromosomal locus under anhydrotetracycline-dependent transcriptional control to establish the correlation between HPrK/P amounts and the efficiency of CCR in Bacillus subtilis. This resulted in about eightfold repression of HPrK/P expression but had no effect on CCR as monitored by xynP'-lacZ reporter gene expression and by analysis of RocG protein amounts. These results suggest that very small amounts of HPrK/P are sufficient for complete CCR and that control of HPrK/P activity depends only on the presence of effectors and not on the abundance of the enzyme.
引用
收藏
页码:147 / 152
页数:6
相关论文
共 28 条
[1]   An enhancer element located downstream of the major glutamate dehydrogenase gene of Bacillus subtilis [J].
Belitsky, BR ;
Sonenshein, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (18) :10290-10295
[2]  
Belitsky BR, 1998, J BACTERIOL, V180, P6298
[3]   CcpA-dependent regulation of Bacillus subtilis glutamate dehydrogenase gene expression [J].
Belitsky, BR ;
Kim, HJ ;
Sonenshein, AL .
JOURNAL OF BACTERIOLOGY, 2004, 186 (11) :3392-3398
[4]   Integrative elements for Bacillus subtilis yielding tetracycline-dependent growth phenotypes -: art. no. E153 [J].
Bertram, R ;
Köstner, M ;
Müller, J ;
Ramos, JV ;
Hillen, W .
NUCLEIC ACIDS RESEARCH, 2005, 33 (18) :1-11
[5]  
Brückner R, 2002, FEMS MICROBIOL LETT, V209, P141
[6]   GLUCOSE AND GLUCOSE-6-PHOSPHATE INTERACTION WITH XYL REPRESSOR PROTEINS FROM BACILLUS SPP MAY CONTRIBUTE TO REGULATION OF XYLOSE UTILIZATION [J].
DAHL, MK ;
SCHMIEDEL, D ;
HILLEN, W .
JOURNAL OF BACTERIOLOGY, 1995, 177 (19) :5467-5472
[7]   ATP-DEPENDENT PROTEIN KINASE-CATALYZED PHOSPHORYLATION OF A SERYL RESIDUE IN HPR, A PHOSPHATE CARRIER PROTEIN OF THE PHOSPHOTRANSFERASE SYSTEM IN STREPTOCOCCUS-PYOGENES [J].
DEUTSCHER, J ;
SAIER, MH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (22) :6790-6794
[8]   PROTEIN KINASE-DEPENDENT HPR/CCPA INTERACTION LINKS GLYCOLYTIC ACTIVITY TO CARBON CATABOLITE REPRESSION IN GRAM-POSITIVE BACTERIA [J].
DEUTSCHER, J ;
KUSTER, E ;
BERGSTEDT, U ;
CHARRIER, V ;
HILLEN, W .
MOLECULAR MICROBIOLOGY, 1995, 15 (06) :1049-1053
[9]   New protein kinase and protein phosphatase families mediate signal transduction in bacterial catabolite repression [J].
Galinier, A ;
Kravanja, M ;
Engelmann, R ;
Hengstenberg, W ;
Kilhoffer, MC ;
Deutscher, J ;
Haiech, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1823-1828
[10]   Phosphorylation of either Crh or HPr mediates binding of CcpA to the Bacillus subtilis xyn cre and catabolite repression of the xyn operon [J].
Galinier, A ;
Deutscher, J ;
Martin-Verstraete, I .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 286 (02) :307-314