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首页> 外文期刊>Food Control >Bacterial dynamics during the spontaneous fermentation of cassava dough in gari production.
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Bacterial dynamics during the spontaneous fermentation of cassava dough in gari production.

机译:木薯面团自发发酵过程中的细菌动力学。

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摘要

The microbial dynamics and diversity during solid substrate fermentation of cassava, a case study of gari production in West Africa, was investigated. The 16S rDNA gene sequence analysis of the PCR-Denaturing Gradient Gel Electrophoresis (PCR-DGGE) analysis of microbial community DNA and Pulsed Field Gel Electrophoresis (PFGE) of selected isolates as well as culturing techniques using different selective media were used to monitor the bacterial dynamics during cassava fermentation. The V3 variable region of the 16S gene was analyzed and the closest relatives of Lactobacillus plantarum, Lactobacillus fermentum, Lactobacillus pentosus, Lactobacillus acidophilus and Lactobacillus casei were identified by sequencing of the DGGE band amplimers. The DGGE amplimers also revealed the succession and dynamics of LAB; there was a progressive increase in their population proportional to the fermentation period. The analysis of the PFGE band patterns showed that five diverse species of LAB were involved in the fermentation. The representative isolate of each of the PFGE clusters was phenotypicaly identified as L. plantarum, L. fermentum and Leuconostoc mesenteroides by the API 50 CHL sugar fermentation profile. These combinations of parameters identified heterofermentative LAB as bacteria that initiated the fermentation, reduced the pH below four and increased the acidity of the fermentation mash. Information such as this is relevant for the development of starter cultures and predictability of the process for traditional fermented foods and to aid their intermediate and large scale production
机译:木薯固体底物发酵过程中的微生物动力学和多样性,以西非加里生产为例。所选菌株的微生物群落DNA PCR-变性梯度凝胶电泳(PCR-DGGE)分析和脉冲场凝胶电泳(PFGE)的16S rDNA基因序列分析以及使用不同选择性培养基的培养技术用于监测细菌木薯发酵过程中的动力学变化。分析了16S基因的V3可变区,并通过DGGE带扩增子的测序鉴定了植物乳杆菌,发酵乳杆菌,戊糖乳杆菌,嗜酸乳杆菌和干酪乳杆菌的近亲。 DGGE放大器还揭示了LAB的继承和动态。与发酵期成正比,种群数量逐渐增加。 PFGE带模式的分析表明,五个不同种类的LAB参与了发酵。通过API 50 CHL糖发酵曲线,在表型上将每个PFGE簇的代表性分离物鉴定为植物乳杆菌,发酵乳杆菌和间肠乳突球菌。这些参数的组合将异源发酵型LAB鉴定为启动发酵,将pH值降低至4以下并提高了发酵mash的酸度的细菌。此类信息与发酵剂文化的发展和传统发酵食品的可预测性有关,并有助于其中间和大规模生产

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