Papadimitriou Minas N B, Resende Catarina, Kuchler Karl, Brul Stanley
Microbiological Control, Unilever Foods Research Centre, Olivier van Noortlaan 120, 3133 AT Vlaardingen, The Netherlands.
Int J Food Microbiol. 2007 Jan 25;113(2):173-9. doi: 10.1016/j.ijfoodmicro.2006.06.035. Epub 2006 Dec 4.
Sorbic acid is a commonly used food preservative against yeast and fungal food spoilage. Understanding its effect on the molecular physiology of yeast cells will allow the food industry to develop knowledge-based strategies to make more optimal use of its preservative action. Here we show that the yeast membrane protein Pdr12, previously shown to be prominently involved in sorbic acid resistance development in laboratory strains, was strongly induced by the presence of sorbic acid in the culture medium in Saccharomyces strains isolated from spoiled foods. Induction of Pdr12 expression was seen both under laboratory conditions and upon growth in a commercial soft drink. Induction was rapid and maintained for the duration of the stress. No Pdr12-like protein induction was seen in Zygosaccharomyces bailii or Zygosaccharomyces lentus, two well-known beverages spoilage organisms. Finally, unexpectedly, our studies showed for the first time that pre-inducing Pdr12p to maximal levels by subjecting cells to a mild sorbic acid stress did not lead to cells with an acquired resistance. Neither more rapid growth in the presence of the acid nor growth at higher sorbic acid concentrations at a given environmental pH was observed. Thus we have shown that while important in resistance development against sorbic acid, by itself induction of the pump is not sufficient to acquire resistance to the preservative.
山梨酸是一种常用的食品防腐剂,可防止酵母和真菌导致的食品变质。了解其对酵母细胞分子生理学的影响,将有助于食品工业制定基于知识的策略,以更优化地利用其防腐作用。在此我们表明,酵母膜蛋白Pdr12先前已证明在实验室菌株中对山梨酸抗性的发展起着重要作用,而在从变质食品中分离出的酿酒酵母菌株中,培养基中存在山梨酸会强烈诱导该蛋白的表达。在实验室条件下以及在商业软饮料中生长时,均观察到Pdr12表达的诱导。诱导迅速且在应激持续期间保持。在两种著名的饮料变质微生物巴氏酵母和鲁氏酵母中未观察到类似Pdr12蛋白的诱导。最后,出乎意料的是,我们的研究首次表明,通过使细胞经受轻度山梨酸应激将Pdr12p预诱导至最高水平,并不会导致细胞获得抗性。在酸存在下既未观察到更快的生长,在给定环境pH值下在更高山梨酸浓度下也未观察到生长。因此我们表明,虽然Pdr12在抗山梨酸方面很重要,但仅诱导该转运蛋白本身不足以获得对防腐剂的抗性。