TY - JOUR
T1 - The Saccharomyces cerevisiae weak-acid-inducible ABC transporter Pdr12 transports fluorescein and preservative anions from the cytosol by an energy-dependent mechanism
AU - Coote, Peter John
AU - Holyoak, C
AU - Bracey, D
AU - Piper, PW
AU - 1, other
PY - 1999/8
Y1 - 1999/8
N2 - 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.
AB - 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.
KW - MEMBRANE H+-ATPASE
KW - HEAT-SHOCK-PROTEIN
KW - ESCHERICHIA-COLI
KW - PLASMA-MEMBRANE
KW - MULTIDRUG-RESISTANCE
KW - INTRACELLULAR PH
KW - FOOD PRESERVATIVES
KW - BENZOIC-ACID
KW - SORBIC ACID
KW - YEAST
UR - http://www.scopus.com/inward/record.url?scp=0032766243&partnerID=8YFLogxK
UR - http://www.journals.asm.org/
M3 - Article
SN - 0021-9193
VL - 181
SP - 4644
EP - 4652
JO - Journal of Bacteriology
JF - Journal of Bacteriology
IS - 15
ER -