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Evolution of fermenting microbiota in tarhana produced under controlled technological conditions

机译:在受控技术条件下生产的塔哈纳发酵菌群的演变

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摘要

The purpose of this study was to evaluate the evolution of lactic acid bacteria (LAB) and yeasts during the fermentation of tarhana produced with some pasteurised ingredients and carried out at 30 and 40 C. The chemical parameters were those typical for tarhana production. Coliform bacteria were not detected during fermentation, while LAB and yeasts were in the range 107e108 colony forming units (CFU) g 1. Plate counts showed an optimal development of both fermenting microbial groups and the differences in cell concentrations were not significant (P > 0.05). LAB were isolated during fermentation and grouped on the basis of phenotypic and polymorphic characteristics. LAB isolates were identified by a combined genetic approach consisting of 16S/23S rRNA intergenic spacer region (ITS) and partial 16S rRNA gene sequencing as Pediococcus acidilactici, Lactobacillus plantarum and Lactobacillus brevis. Hence, the pas- teurisation of the vegetable ingredients, excluded wheat flour, enhanced the hygienic conditions of tarhana without influencing the normal evolution of LAB. However, the fermentation at 40 C favoured pediococci, while the production at 30 C was mainly characterised by lactobacilli. Yeasts, identified by the restriction fragment length polymorphism (RFLP) of the 5.8S ITS rRNA gene, were mainly represented by the species Saccharomyces cerevisiae in both productions.
机译:这项研究的目的是评估在30和40℃下用某些巴氏杀菌成分生产的塔尔哈纳发酵过程中乳酸菌(LAB)和酵母的演变。化学参数是塔尔哈纳生产的典型化学参数。在发酵过程中未检测到大肠菌,而LAB和酵母菌的菌落形成范围在107e108个菌落形成单位(CFU)g 1范围内。板计数显示了两个发酵微生物组的最佳发育,并且细胞浓度的差异也不显着(P> 0.05)。 )。乳酸菌在发酵过程中被分离出来,并根据表型和多态性特征进行分组。通过组合遗传方法鉴定了LAB分离株,该方法由16S / 23S rRNA基因间隔区(ITS)和部分16S rRNA基因测序组成,如乳酸杆菌,植物乳杆菌和短乳杆菌。因此,除小麦粉外,蔬菜成分的巴氏杀菌增强了塔尔哈纳的卫生条件,而不会影响LAB的正常进化。但是,在40℃下发酵有利于pedococicci,而在30℃下的生产主要以乳酸菌为特征。通过5.8S ITS rRNA基因的限制性片段长度多态性(RFLP)鉴定的酵母,在两种产品中主要以酿酒酵母(Saccharomyces cerevisiae)物种为代表。

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