Transcriptional activation of the citrate permease P gene of Lactococcus lactis biovar diacetylactis by an insertion sequence like element present in plasmid pCIT264

被引:27
作者
deFelipe, FL
Magni, C
deMendoza, D
Lopez, P
机构
[1] CSIC, CTR INVEST BIOL, E-28006 MADRID, SPAIN
[2] UNIV NACL ROSARIO, FAC CIENCIAS BIOQUIM & FARMACEUT, DEPT MICROBIOL, RA-2000 ROSARIO, ARGENTINA
来源
MOLECULAR AND GENERAL GENETICS | 1996年 / 250卷 / 04期
关键词
transcriptional activation; Lactococcus lactis; Escherichia coli; plasmid pCIT264; expression of citP gene;
D O I
10.1007/s004380050095
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
The lactococcal plasmid pCIT264 contains a cluster of three genes (citQ, citR and citP) involved in the transport of citrate in Lactococcus lactis biovar diacetylactis. The cit cluster contains a copy of a newly discovered insertion sequence (IS)-like element located between its promoter P1 and the first gene of the cluster. In this report, we show that this IS-like element can act as a mobile switch for the downstream genes, creating two new transcriptional promoters named P2 and P2'. The P2 promoter is recognized by the lactococcal RNA polymerase in vivo. This is a hybrid promoter composed of a -35 region reading outwards 12 bp from the right end of the IS-like element, and a nucleotide sequence from the recipient plasmid, adjacent to the element, which provides an appropriately spaced -10 region. Transcription of the citQRP cluster from this promoter takes place during the exponential and stationary phases of growth in L. lactis. Promoter P2' is included in the IS-like element and is the only promoter responsible for expression of citP in E. coli. Thus, it appears that the introduction of this element into pCIT264 allows expression of the citQRP cluster in E. coli, and increases its levels of expression in L. lactis.
引用
收藏
页码:428 / 436
页数:9
相关论文
共 30 条
[1]   BACTERIAL PLASMIDS AND GENE FLUX [J].
AMABILECUEVAS, CF ;
CHICUREL, ME .
CELL, 1992, 70 (02) :189-199
[2]   PHAGE ABORTIVE INFECTION MECHANISM FROM LACTOCOCCUS-LACTIS SUBSP LACTIS, EXPRESSION OF WHICH IS MEDIATED BY AN ISO-ISS1 ELEMENT [J].
CLUZEL, PJ ;
CHOPIN, A ;
EHRLICH, SD ;
CHOPIN, MC .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (12) :3547-3551
[3]   NUCLEOTIDE-SEQUENCE AND EXPRESSION IN ESCHERICHIA-COLI OF THE LACTOCOCCUS-LACTIS CITRATE PERMEASE GENE [J].
DAVID, S ;
VANDERREST, ME ;
DRIESSEN, AJM ;
SIMONS, G ;
DEVOS, WM .
JOURNAL OF BACTERIOLOGY, 1990, 172 (10) :5789-5794
[4]   CITRATE UTILIZATION GENE-CLUSTER OF THE LACTOCOCCUS-LACTIS BIOVAR DIACETYLACTIS - ORGANIZATION AND REGULATION OF EXPRESSION [J].
DEFELIPE, FL ;
MAGNI, C ;
DEMENDOZA, D ;
LOPEZ, P .
MOLECULAR & GENERAL GENETICS, 1995, 246 (05) :590-599
[5]   COMPARATIVE-ANALYSIS OF GENE-EXPRESSION IN STREPTOCOCCUS-PNEUMONIAE AND LACTOCOCCUS-LACTIS [J].
DEFELIPE, FL ;
CORRALES, MA ;
LOPEZ, P .
FEMS MICROBIOLOGY LETTERS, 1994, 122 (03) :289-295
[6]   HIGH-EFFICIENCY ELECTROPORATION OF LACTOCOCCUS-LACTIS SUBSP LACTIS LM0230 WITH PLASMID PGB301 [J].
DORNAN, S ;
COLLINS, MA .
LETTERS IN APPLIED MICROBIOLOGY, 1990, 11 (02) :62-64
[7]   DETERMINATION OF AN RNA STRUCTURE INVOLVED IN SPLICING INHIBITION OF A MUSCLE-SPECIFIC EXON [J].
DORVAL, BC ;
DAUBENTONCARAFA, Y ;
MARIE, J ;
BRODY, E .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 221 (03) :837-856
[8]  
GALAS DJ, 1989, MOBILE DNA, P109
[9]  
GASSON MJ, 1993, FEMS MICROBIOL REV, V12, P3, DOI [10.1016/0168-6445(93)90055-E, 10.1111/j.1574-6976.1993.tb00010.x]
[10]  
GASSON MJ, 1983, J BACTERIOL, V154, P1