Integration of signals through Crc and PtsN in catabolite repression of Pseudomonas putida TOL plasmid pWW0

被引:66
作者
Aranda-Olmedo, I [1 ]
Ramos, JL [1 ]
Marqués, S [1 ]
机构
[1] EEZ CSIC, Dept Biochem & Mol & Cellular Biol Plants, E-18080 Granada, Spain
关键词
D O I
10.1128/AEM.71.8.4191-4198.2005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Toluene degradation in Pseudomonas putida KT2440 pWW0 plasmid is subjected to catabolite repression. Pu and Psi promoters of the pWW0 TOL plasmid are down-regulated in vivo during exponential growth in rich medium. In cells growing on minimal medium, yeast extract (YE) addition mimics exponential-phase rich medium repression of these promoters. We have constructed and tested mutants in a series of global regulators described in Pseudomonas. We describe that a mutant in ere (catabolite repression control) partially relieves YE repression. Macroarray experiments show that crc transcription is strongly increased in the presence of YF, inversely correlated with TOL pathway expression. On the other hand, we have found that induced levels of expression from Pu and P-s in the presence of YE are partially derepressed in a ptsN mutant of P. putida. PtsN but not Crc seems to directly interfere with XylR activation at target promoters. The effect of the double mutation in ptsN and ere is not the sum of the effects of each independent mutation and suggests that both regulators are elements of a common regulatory pathway. Basal expression levels from these promoters in the absence of inducer are still XylR dependent and are also repressed in the presence of yeast extract. Neither crc nor ptsN could relieve this repression.
引用
收藏
页码:4191 / 4198
页数:8
相关论文
共 51 条
[1]  
ABRIL MA, 1991, J BIOL CHEM, V266, P15832
[2]   SPECIFIC-PURPOSE PLASMID CLONING VECTORS .2. BROAD HOST RANGE, HIGH COPY NUMBER, RSF1010-DERIVED VECTORS, AND A HOST-VECTOR SYSTEM FOR GENE CLONING IN PSEUDOMONAS [J].
BAGDASARIAN, M ;
LURZ, R ;
RUCKERT, B ;
FRANKLIN, FCH ;
BAGDASARIAN, MM ;
FREY, J ;
TIMMIS, KN .
GENE, 1981, 16 (1-3) :237-247
[3]   Activation of the toluene-responsive regulator XyIR causes a transcriptional switch between σ54 and σ70 promoters at the divergent Pr/Ps region of the TOL plasmid [J].
Bertoni, G ;
Marqués, S ;
de Lorenzo, V .
MOLECULAR MICROBIOLOGY, 1998, 27 (03) :651-659
[4]   Construction and use of a versatile set of broad-host-range cloning and expression vectors based on the RK2 replicon [J].
Blatny, JM ;
Brautaset, T ;
WintherLarsen, HC ;
Haugan, K ;
Valla, S .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (02) :370-379
[5]   Expression systems and physiological control of promoter activity in bacteria [J].
Cases, I ;
de Lorenzo, V .
CURRENT OPINION IN MICROBIOLOGY, 1998, 1 (03) :303-310
[6]   The IIANtr (PtsN) protein of Pseudomonas putida mediates the C source inhibition of the σ54-dependent Pu promoter of the TOL plasmid [J].
Cases, I ;
Pérez-Martín, J ;
de Lorenzo, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (22) :15562-15568
[7]   Involvement of sigma(54) in exponential silencing of the Pseudomonas putida TOL plasmid Pu promoter [J].
Cases, I ;
deLorenzo, V ;
PerezMartin, J .
MOLECULAR MICROBIOLOGY, 1996, 19 (01) :7-17
[8]   Role of ptsO in carbon-mediated inhibition of the Pu promoter belonging to the pWWO Pseudomonas putida plasmid [J].
Cases, I ;
Velázquez, F ;
de Lorenzo, V .
JOURNAL OF BACTERIOLOGY, 2001, 183 (17) :5128-5133
[9]   The black cat/white cat principle of signal integration in bacterial promoters [J].
Cases, I ;
de Lorenzo, V .
EMBO JOURNAL, 2001, 20 (1-2) :1-11
[10]   Evidence of multiple regulatory functions for the PtsN (IIANtr) protein of Pseudomonas putida [J].
Cases, I ;
Lopez, JA ;
Albar, JP ;
De Lorenzo, V .
JOURNAL OF BACTERIOLOGY, 2001, 183 (03) :1032-1037