The cefT gene of Acremonium chrysogenum C10 encodes a putative multidrug efflux pump protein that significantly increases cephalosporin C production

被引:75
作者
Ullán, RV
Liu, G
Casqueiro, J
Gutiérrez, S
Bañuelos, O
Martín, JF [1 ]
机构
[1] Univ Leon, Fac Biol & Environm Sci, Area Microbiol, E-24071 Leon, Spain
[2] Inst Biotechnol, Leon 24006, Spain
关键词
Acremonium chrysogenum; cephalosporin; antibiotic secretion; MFS; multidrug efflux-pumps;
D O I
10.1007/s00438-002-0702-5
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
Transcriptional analysis of the region downstream of the pcbAB gene (which encodes the a-aminoadipyl-cysteinyl-valine synthetase involved in cephalosporin synthesis) of Acremonium chrysogenum revealed the presence of two different transcripts corresponding to two new ORFs. ORF3 encodes a putative D-hydroxyacid dehydrogenase and cefT (for transmembrane protein) encodes a multidrug efflux pump belonging to the Major Faciltator Superfamily (MFS) of membrane proteins. The CefT protein has 12 transmembrane segments (TMS) and contains motifs A, B, C, D2 and G characteristic of the Drug:H+ antiporter 12-TMS group of the major facilitator superfamily. The CefT protein confers resistance to some toxic organic acids, including isovaleric acid and phenylacetic acid. Targeted inactivation of ORF3 and cefT by gene replacement showed that they are pot essential for cephalosporin biosynthesis. However, amplification of the cefT gene results in increments of up to 100% in cephalosporin production in the A, chrysogenum C10 strain. Amplification of a truncated form of the cefT insert did not lead to cephalosporin overproduction. It seems that the CefT protein is involved in cephalosporin export from A. chrysogenum or in transmembrane signal transduction, and that there are redundant systems involved in cephalosporin export.
引用
收藏
页码:673 / 683
页数:11
相关论文
共 48 条
[31]   QUINOLONE RESISTANCE MEDIATED BY NORA - PHYSIOLOGICAL CHARACTERIZATION AND RELATIONSHIP TO FLQB, A QUINOLONE RESISTANCE LOCUS ON THE STAPHYLOCOCCUS-AUREUS CHROMOSOME [J].
NG, EYW ;
TRUCKSIS, M ;
HOOPER, DC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (06) :1345-1355
[32]  
Pao SS, 1998, MICROBIOL MOL BIOL R, V62, P1
[33]   TOPOLOGY, STRUCTURE AND EVOLUTION OF 2 FAMILIES OF PROTEINS INVOLVED IN ANTIBIOTIC AND ANTISEPTIC RESISTANCE IN EUKARYOTES AND PROKARYOTES - AN ANALYSIS [J].
PAULSEN, IT ;
SKURRAY, RA .
GENE, 1993, 124 (01) :1-11
[34]   Proton-dependent multidrug efflux systems [J].
Paulsen, IT ;
Brown, MH ;
Skurray, RA .
MICROBIOLOGICAL REVIEWS, 1996, 60 (04) :575-+
[35]   A regulatory gene (ccaR) required for cephamycin and clavulanic acid production in Streptomyces clavuligerus: Amplification results in overproduction of both beta-lactam compounds [J].
PerezLlarena, FJ ;
Liras, P ;
RodriguezGarcia, A ;
Martin, JF .
JOURNAL OF BACTERIOLOGY, 1997, 179 (06) :2053-2059
[36]   TRANSFORMATION OF ASPERGILLUS BASED ON THE HYGROMYCIN-B RESISTANCE MARKER FROM ESCHERICHIA-COLI [J].
PUNT, PJ ;
OLIVER, RP ;
DINGEMANSE, MA ;
POUWELS, PH ;
VANDENHONDEL, CAMJJ .
GENE, 1987, 56 (01) :117-124
[37]  
RAMOS FR, 1986, FEMS MICROBIOL LETT, V35, P123, DOI 10.1111/j.1574-6968.1986.tb01513.x
[38]  
REVILLA G, 1983, THESIS U LEON SPAIN
[39]  
Sambrook J., 2002, MOL CLONING LAB MANU
[40]   ISOLATION, SEQUENCE DETERMINATION AND EXPRESSION IN ESCHERICHIA-COLI OF THE ISOPENICILLIN-N SYNTHETASE GENE FROM CEPHALOSPORIUM-ACREMONIUM [J].
SAMSON, SM ;
BELAGAJE, R ;
BLANKENSHIP, DT ;
CHAPMAN, JL ;
PERRY, D ;
SKATRUD, PL ;
VANFRANK, RM ;
ABRAHAM, EP ;
BALDWIN, JE ;
QUEENER, SW ;
INGOLIA, TD .
NATURE, 1985, 318 (6042) :191-194