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首页> 外文期刊>Applied Microbiology and Biotechnology >Phenotypic and genotypic screening of human-originated lactobacilli for vitamin B-12 production potential: process validation by micro-assay and UFLC
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Phenotypic and genotypic screening of human-originated lactobacilli for vitamin B-12 production potential: process validation by micro-assay and UFLC

机译:人类起源的乳酸菌的维生素B-12生产潜力的表型和基因型筛选:通过微分析和UFLC进行工艺验证

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摘要

Vitamin B-12 (B-12) production is a strain specific, rare and hidden functional attribute of lactobacilli and a cogent protocol for selection of such isolates from the herd of lactobacilli is required. The present study included isolation of lactobacilli from human samples (milk and fecal), screening them by a polyphasic (three-phase) methodology for probable B-12 production potential and validating the screening protocol by exploring selected strains for in vitro vitamin production (two-phase fermentation) and quantification [micro-assay and ultra fast liquid chromatography (UFLC)]. Fifty-nine Lactobacillus strains were recovered from tested biological samples. Contrary to screening inapplicabilities of first [growth potential (GP) in B-12-free medium] and second phases (GP in B-12-free and cobalt chloride-supplemented conditions), third phase (cbiK gene detection on genomic DNA) alone was revealed as a validated strategy for selection of two probable B-12-producing lactobacilli. Microbiological assay confirmed production and bioavailability of produced vitamin, while UFLC testing validated the results by precisely quantifying the cyanocobalamin (industrially produced bio-available form of B-12) in cell extracts of both possible B12 producers [BHM10 (10.91 +/- 1.55 mu g/l) and BCF20 (23.90 +/- 1.73 mu g/l)] and positive standard [Lactobacillus reuteri DSM20016 (20.03 +/- 4.17 mu g/l)]. Moreover, this study generates a novel report for genomic detection, partial amplification and sequencing of cbiK gene in Lactobacillus plantarum species (both BHM10 and BCF20). In conclusion, contrary to first two phases, cbiK gene detection strategy successfully selects B-12-producing strains from a group of human-originated lactobacilli and can be used in the future for similar screening studies.
机译:维生素B-12(B-12)的产生是乳杆菌的一种菌株特有的,罕见的和隐藏的功能属性,因此需要有力的方案从乳杆菌群中选择这种分离物。本研究包括从人类样品(牛奶和粪便)中分离乳酸杆菌,通过多相(三相)方法筛选可能的B-12生产潜力,并通过探索体外生产维生素的选定菌株来验证筛选方案(两个相发酵)和定量分析[微量分析和超快速液相色谱(UFLC)]。从测试的生物样品中回收了59株乳酸杆菌菌株。与筛选第一阶段[不含B-12的培养基中的生长潜能(GP)]和第二阶段(不含B-12的氯和补充氯化钴的条件下的GP),第三阶段(在基因组DNA上检测cbiK基因)的不适用性相反作为选择两种可能的产生B-12的乳酸菌的有效策略,有人发现了这种细菌。微生物测定证实了所产生维生素的生产和生物利用度,而UFLC测试通过精确定量两种可能的B12产生者[BHM10(10.91 +/- 1.55 mu g / l)和BCF20(23.90 +/- 1.73μg / l)和阳性标准品[罗伊氏乳杆菌DSM20016(20.03 +/- 4.17μg / l)]。此外,这项研究为植物乳杆菌(BHM10和BCF20)中cbiK基因的基因组检测,部分扩增和测序提供了新的报道。总而言之,与前两个阶段相反,cbiK基因检测策略成功地从一组人类起源的乳酸杆菌中选择了产生B-12的菌株,并可以在将来用于类似的筛选研究。

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