Suppr超能文献

通过在酿酒酵母中表达嗜酸乳杆菌片球菌素基因(pedA)来开发杀菌酵母菌株。

The development of bactericidal yeast strains by expressing the Pediococcus acidilactici pediocin gene (pedA) in Saccharomyces cerevisiae.

作者信息

Schoeman H, Vivier M A, Du Toit M, Dicks L M, Pretorius I S

机构信息

Institute for Wine Biotechnology, University of Stellenbosch, South Africa.

出版信息

Yeast. 1999 Jun 15;15(8):647-56. doi: 10.1002/(SICI)1097-0061(19990615)15:8<647::AID-YEA409>3.0.CO;2-5.

Abstract

The excessive use of sulphur dioxide and other chemical preservatives in wine, beer and other fermented food and beverage products to prevent the growth of unwanted microbes holds various disadvantages for the quality of the end-products and is confronted by mounting consumer resistance. The objective of this study was to investigate the feasibility of controlling spoilage bacteria during yeast-based fermentations by engineering bactericidal strains of Saccharomyces cerevisiae. To test this novel concept, we have successfully expressed a bacteriocin gene in yeast. The pediocin operon of Pediococcus acidilactici PAC1.0 consists of four clustered genes, namely pedA (encoding a 62 amino acid precursor of the PA-1 pediocin), pedB (encoding an immunity factor), pedC (encoding a PA-1 transport protein) and pedD (encoding a protein involved in the transport and processing of PA-1). The pedA gene was inserted into a yeast expression/secretion cassette and introduced as a multicopy episomal plasmid into a laboratory strain (Y294) of S. cerevisiae. Northern blot analysis confirmed that the pedA structural gene in this construct (ADH1P-MFa1S-pedA-ADH1T, designated PED1), was efficiently expressed under the control of the yeast alcohol dehydrogenase I gene promoter (ADH1P) and terminator (ADH1T). Secretion of the PED1-encoded pediocin PA-1 was directed by the yeast mating pheromone alpha-factor's secretion signal (MFa1S). The presence of biologically active antimicrobial peptides produced by the yeast transformants was indicated by agar diffusion assays against sensitive indicator bacteria (e.g. Listeria monocytogenes B73). Protein analysis indicated the secreted heterologous peptide to be approximately 4.6 kDa, which conforms to the expected size. The heterologous peptide was present at relatively low levels in the yeast supernatant but pediocin activity was readily detected when intact yeast colonies were used in sensitive strain overlays. This study could lead to the development of bactericidal yeast strains where S. cerevisiae starter cultures not only conduct the fermentations in the wine, brewing and baking industries but also act as biological control agents to inhibit the growth of spoilage bacteria.

摘要

在葡萄酒、啤酒及其他发酵食品和饮料产品中过度使用二氧化硫及其他化学防腐剂来防止有害微生物生长,会给最终产品质量带来诸多不利影响,且面临着消费者越来越大的抵制。本研究的目的是通过构建具有杀菌能力的酿酒酵母菌株,来探究在基于酵母的发酵过程中控制腐败细菌的可行性。为验证这一新颖概念,我们已成功在酵母中表达了一种细菌素基因。嗜酸乳杆菌PAC1.0的片球菌素操纵子由四个成簇基因组成,即pedA(编码PA-1片球菌素的62个氨基酸前体)、pedB(编码免疫因子)、pedC(编码PA-1转运蛋白)和pedD(编码参与PA-1转运和加工的蛋白质)。将pedA基因插入酵母表达/分泌盒,并作为多拷贝附加体质粒导入酿酒酵母的实验室菌株(Y294)。Northern印迹分析证实,该构建体(ADH1P-MFa1S-pedA-ADH1T,命名为PED1)中的pedA结构基因在酵母乙醇脱氢酶I基因启动子(ADH1P)和终止子(ADH1T)的控制下有效表达。PED1编码的片球菌素PA-1的分泌由酵母交配信息素α-因子的分泌信号(MFa1S)引导。通过针对敏感指示菌(如单核细胞增生李斯特菌B73)的琼脂扩散试验表明,酵母转化体产生了具有生物活性的抗菌肽。蛋白质分析表明,分泌的异源肽大小约为4.6 kDa,与预期大小相符。异源肽在酵母上清液中的含量相对较低,但当完整的酵母菌落用于敏感菌株覆盖试验时,很容易检测到片球菌素活性。本研究可能会促成杀菌酵母菌株的开发,在葡萄酒、酿造和烘焙行业中,酿酒酵母起始培养物不仅能进行发酵,还能作为生物控制剂抑制腐败细菌的生长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验