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Taxonomic structure and monitoring of the dominant lactic acid bacteria population during wheat flour sourdough type I propagation by using Lactobacillus sanfranciscensis starters

机译:利用旧金山乳杆菌发酵剂对I型小麦粉发酵过程中主要乳酸菌种群的分类结构和监测

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摘要

The structure and stability of the dominant lactic acid bacterium population were assessed during wheat flour sourdough type I propagation by using singly nine strains of Lactobacillus sanfranciscensis. Under back-slopping propagation with wheat flour type 0 F114, cell numbers of presumptive lactic acid bacteria varied slightly between and within starters. As determined by randomly amplified polymorphic DNA-PCR and restriction endonuclease analysis-pulsed-field gel electrophoresis analyses, only three (LS8, LS14, and LS44) starters dominated throughout 10 days of propagation. The others progressively decreased to less than 3 log CFU g−1. Partial sequence analysis of the 16S rRNA and recA genes and PCR-denaturating gradient gel electrophoresis analysis using the rpoB gene allowed identification of Weissella confusa, Lactobacillus sanfranciscensis, Lactobacillus plantarum, Lactobacillus rossiae, Lactobacillus brevis, Lactococcus lactis subsp. lactis, Pediococcus pentosaceus, and Lactobacillus spp. as the dominant species of the raw wheat flour. At the end of propagation, one autochthonous strain of L. sanfranciscensis was found in all the sourdoughs. Except for L. brevis, strains of the above species were variously found in the mature sourdoughs. Persistent starters were found in association with other biotypes of L. sanfranciscensis and with W. confusa or L. plantarum. Sourdoughs were characterized for acidification, quotient of fermentation, free amino acids, and community-level catabolic profiles by USING Biolog 96-well Eco microplates. In particular, catabolic profiles of sourdoughs containing persistent starters behaved similarly and were clearly differentiated from the others. The three persistent starters were further used for the production of sourdoughs and propagated by using another wheat flour whose lactic acid bacterium population in part differed from the previous one. Also, in this case all three starter strains persisted during propagation.
机译:通过分别使用9株Sanfranciscensis乳酸菌评估了I型小麦粉发酵过程中主要乳酸菌种群的结构和稳定性。在0 F114型小麦面粉的反向倾斜繁殖下,假定的乳酸菌的细胞数在发酵剂之间和发酵剂内部略有不同。如通过随机扩增的多态性DNA-PCR和限制性内切核酸酶分析-脉冲场凝胶电泳分析所确定,在整个繁殖10天中,只有三个(LS8,LS14和LS44)起始剂占主导地位。其他的逐渐降低到小于3 log CFU g-1。通过对16S rRNA和recA基因进行部分序列分析以及使用rpoB基因进行PCR变性梯度凝胶电泳分析,可以鉴定魏氏菌,旧金山乳杆菌,植物乳杆菌,罗氏乳杆菌,短乳杆菌,乳酸乳球菌亚种。乳酸菌,戊糖小球菌和乳酸杆菌属。作为原料小麦粉的主要品种。繁殖结束时,在所有酵母中都发现了一种桑弗朗西斯菌的本地种。除了短乳杆菌以外,在成熟的酸面团中还发现了上述种的菌株。持久性发酵剂被发现与Sanfranciscensis的其他生物型以及Confus或usa L. plantarum有关。通过使用Biolog 96孔Eco微孔板,对酸面团进行酸化,发酵商,游离氨基酸和社区水平的分解代谢特性进行表征。尤其是,含有持久性发酵剂的酵母的分解代谢特性表现相似,并且与其他发酵剂明显不同。这三个持久性发酵剂被进一步用于生产酸面团,并使用另一种小麦粉进行繁殖,该小麦粉的乳酸菌种群与先前的有所不同。同样,在这种情况下,所有三个起始菌株都在繁殖过程中持续存在。

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