首页> 外文期刊>Antonie van Leeuwenhoek: Journal of Microbiology and serology >An in vitro study of Lactobacillus plantarum strains for the presence of plantaricin genes and their potential control of the table olive microbiota.
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An in vitro study of Lactobacillus plantarum strains for the presence of plantaricin genes and their potential control of the table olive microbiota.

机译:植物霉素基因存在的乳酸杆菌菌株的体外研究及其对表橄榄微生物的潜在控制。

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摘要

Sixteen Lactobacillus plantarum strains, isolated from fermented table olives, were studied for the presence and expression of genes involved in the production of bacteriocins, pheromones and other peptides. The presence of 13 genes that belong to pln locus was monitored, while for the study of gene expression, producer strains were cultured in growth medium with variant salinity (0, 4, 6, and 8?% NaCl) and pH (3.5, 4.0, 4.5, and 6.4). The effect of producer strain on the growth of indicator microorganisms was evaluated using a well diffusion assay. In parallel, Real-Time PCR was employed to monitor the genetic expression of plnE/F and plnJ/K genes for strains that revealed the highest antimicrobial activity. The well diffusion assay showed that the growth of Lactobacillus pentosus was inhibited by six L. plantarum strains when cultured on control medium (0?% NaCl, pH 6.4). Moreover, when the same growth medium was supplemented with 4 and 6?% NaCl, the growth of L. pentosus was inhibited by three and two L. plantarum strains, respectively. Growth of L. pentosus was favoured when L. plantarum strains were cultured on a growth medium with lowered pH (3.5, 4.0, and 4.5). No inhibition of pathogens was observed, but in a few cases, inhibition of Aureobasidium pullulans was detected. The Real-Time PCR assay revealed that the expression of genes was dependent on producer strains and growth phase, whereas inhibition of indicator strains was enhanced in earlier stages of the growth curve in the presence of NaCl, although similar counts were obtained.
机译:研究了从发酵的表橄榄中分离的植物蘑菇菌株,用于涉及产生的基因,信息素,信息素和其他肽的基因的存在和表达。监测属于PLN基因座的13个基因的存在,同时对于基因表达的研究,在具有变体盐度(0,4,6和8→%NaCl)和pH的生长培养基中培养生产者菌株(3.5,4.0 ,4.5和6.4)。使用孔扩散测定评估生产者菌株对指示剂微生物生长的影响。并行地,采用实时PCR监测PLNE / F和PLNJ / K基因的遗传表达,用于显示最高抗微生物活性的菌株。孔的扩散测定表明,当在对照培养基上培养时,乳杆菌菌株的生长抑制了六杆跖骨菌株(0〜%NaCl,pH6.4)。此外,当补充相同的生长培养基时,含有4和6μl的NaCl,分别抑制了L. pentosus的生长。当L.Purtarum菌株在具有降低的pH(3.5,4.0和4.5)的生长培养基上培养L.Purtarum菌株时,L. pentosus的生长受到青睐。未观察到对病原体的抑制,但在几个情况下,检测到抑制不亚哌糊糊l藜。实时PCR测定表明,基因的表达依赖于生产者菌株和生长阶段,而在NaCl存在下,在NaCl存在下的生长曲线的早期阶段中抑制指标菌株的抑制,尽管获得了类似的计数。

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