The Saccharomyces cerevisiae weak-acid-inducible ABC transporter pdr12 transports fluorescein and preservative anions from the cytosol by an energy-dependent mechanism

被引:135
作者
Holyoak, CD
Bracey, D
Piper, PW
Kuchler, K
Coote, PJ [1 ]
机构
[1] Unilever Res Colworth, Dept Microbiol, Sharnbrook MK44 1LQ, Beds, England
[2] UCL, Dept Biochem & Mol Biol, London WC1E 6BT, England
[3] Univ Vienna, Dept Mol Genet, A-1030 Vienna, Austria
[4] Bioctr Vienna, A-1030 Vienna, Austria
关键词
D O I
10.1128/JB.181.15.4644-4652.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Growth of Saccharomyces cerevisiae in the presence of the weak-acid preservative sorbic acid results in the induction of the ATP-binding cassette (ABC) transporter Pdr12 in the plasma membrane (P, Piper, Y, Mahe, S, Thompson, R. Pandjaitan, C. Holyoak, R, Egner, M. Muhlbauer, P. Coote, and K. Kuchler, EMBO J, 17:4257-4265, 1998). Pdr12 appears to mediate resistance to water-soluble, monocarboxylic acids with chain lengths of from C-1 to C-7. Exposure to acids with aliphatic chain lengths greater than C-7 resulted in no observable sensitivity of Delta pdr12 mutant cells compared to the parent. Parent and Delta pdr12 mutant cells were grown in the presence of sorbic acid and subsequently loaded with fluorescein. Upon addition of an energy source in the form of glucose, parent cells immediately effluxed fluorescein from the cytosol into the surrounding medium. In contrast, under the same conditions, cells of the Delta pdr12 mutant were unable to efflux any of the dye. When both parent and Delta pdr12 mutant cells were grown without sorbic acid and subsequently loaded with fluorescein, upon the addition of glucose no efflux of fluorescein was detected from either strain. Thus, we have shown that Pdr12 catalyzes the energy-dependent extrusion of fluorescein from the cytosol. Lineweaver-Burk analysis revealed that sorbic and benzoic acids competitively inhibited ATP-dependent fluorescein efflux, Thus, these data provide strong evidence that sorbate and benzoate anions compete with fluorescein for a putative monocarboxylate binding site on the Pdr12 transporter.
引用
收藏
页码:4644 / 4652
页数:9
相关论文
共 42 条
[31]  
2
[32]   FUNCTIONAL EXPRESSION OF P-GLYCOPROTEIN ENCODED BY THE MOUSE MDR3 GENE IN YEAST-CELLS [J].
RUETZ, S ;
RAYMOND, M ;
GROS, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11588-11592
[33]   PHOSPHATIDYLCHOLINE TRANSLOCASE - A PHYSIOLOGICAL-ROLE FOR THE MDR2 GENE [J].
RUETZ, S ;
GROS, P .
CELL, 1994, 77 (07) :1071-1081
[34]   ANOTHER EXPLANATION FOR THE TOXICITY OF FERMENTATION ACIDS AT LOW PH - ANION ACCUMULATION VERSUS UNCOUPLING [J].
RUSSELL, JB .
JOURNAL OF APPLIED BACTERIOLOGY, 1992, 73 (05) :363-370
[35]  
SALMOND CV, 1984, J GEN MICROBIOL, V130, P2845
[36]  
Serrano R, 1991, MOL CELLULAR BIOL YE, P523
[37]   GENE SNQ2 OF SACCHAROMYCES-CEREVISIAE, WHICH CONFERS RESISTANCE TO 4-NITROQUINOLINE-N-OXIDE AND OTHER CHEMICALS, ENCODES A 169-KDA PROTEIN HOMOLOGOUS TO ATP-DEPENDENT PERMEASES [J].
SERVOS, J ;
HAASE, E ;
BRENDEL, M .
MOLECULAR AND GENERAL GENETICS, 1993, 236 (2-3) :214-218
[38]  
STEVENS S, 1993, APPL MICROBIOL BIOT, V38, P656
[39]  
THEVELEIN JM, 1987, J GEN MICROBIOL, V133, P2197
[40]   EFFECT OF BENZOIC-ACID ON METABOLIC FLUXES IN YEASTS - A CONTINUOUS-CULTURE STUDY ON THE REGULATION OF RESPIRATION AND ALCOHOLIC FERMENTATION [J].
VERDUYN, C ;
POSTMA, E ;
SCHEFFERS, WA ;
VANDIJKEN, JP .
YEAST, 1992, 8 (07) :501-517