Laboratory of Microbiology and Biotechnology of Foods, Agricultural University of Athens, Iera Odos 75, 11855, Athens, Greece.
Antonie Van Leeuwenhoek. 2013 Apr;103(4):821-32. doi: 10.1007/s10482-012-9864-2. Epub 2012 Dec 9.
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.
从发酵橄榄中分离出的 16 株植物乳杆菌菌株,研究了其与细菌素、信息素和其他肽类产生相关的基因的存在和表达情况。监测了属于 pln 基因座的 13 个基因的存在,而对于基因表达的研究,生产菌株在具有不同盐度(0、4、6 和 8% NaCl)和 pH(3.5、4.0、4.5 和 6.4)的生长培养基中进行培养。使用孔扩散测定法评估了生产菌株对指示微生物生长的影响。同时,使用实时 PCR 监测plnE/F 和 plnJ/K 基因的遗传表达,这些基因在显示出最高抗菌活性的菌株中进行监测。孔扩散测定法表明,当在对照培养基(0%NaCl,pH6.4)上培养时,有 6 株植物乳杆菌菌株抑制了戊糖乳杆菌的生长。此外,当相同的生长培养基中添加 4%和 6%NaCl 时,分别有 3 株和 2 株植物乳杆菌菌株抑制了戊糖乳杆菌的生长。当植物乳杆菌菌株在降低 pH(3.5、4.0 和 4.5)的生长培养基中培养时,戊糖乳杆菌的生长受到促进。未观察到对病原体的抑制,但在少数情况下,检测到对出芽短梗霉的抑制。实时 PCR 分析表明,基因表达取决于生产菌株和生长阶段,尽管在 NaCl 存在的情况下,生长曲线的早期阶段会增强对指示菌株的抑制,但获得了类似的计数。