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首页> 外文期刊>Journal of Microbiological Methods >Qualitative detection of class IIa bacteriocinogenic lactic acid bacteria from traditional Chinese fermented food using a YGNGV-motif-based assay.
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Qualitative detection of class IIa bacteriocinogenic lactic acid bacteria from traditional Chinese fermented food using a YGNGV-motif-based assay.

机译:使用基于YGNGV基序的分析方法定性检测中国传统发酵食品中IIa类致细菌性乳酸菌。

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In the present study, a YGNGV-motif-based assay was developed and applied. Given that there is an increasing demand for natural preservatives, we set out to obtain lactic acid bacteria (LAB) that produce bacteriocins against Gram-positive and Gram-negative bacteria. We here isolated 123 LAB strains from 5 types of traditional Chinese fermented food and screened them for the production of bacteriocins using the agar well diffusion assay (AWDA). Then, to acquire LAB producing class IIa bacteriocins, we used a YGNGV-motif-based assay that was based on 14 degenerate primers matching all class IIa bacteriocin-encoding genes currently deposited in NCBI. Eight of the LAB strains identified by AWDA could inhibit Gram-positive and Gram-negative bacteria; 5 of these were YGNGV-amplicon positive. Among these 5 isolates, amplicons from 2 strains (Y31 and Y33) matched class IIa bacteriocin genes. Strain Y31 demonstrated the highest inhibitory activity and the best match to a class IIa bacteriocin gene in NCBI, and was identified as Enterococcus faecium. The bacteriocin from Enterococcus avium Y33 was 100% identical to enterocin P. Both of these strains produced bacteriocins with strong antimicrobial activity against Listeria monocytogenes, Escherichia coli, and Bacillus subtilis, hence these bacteriocins hold promise as potential bio-preservatives in the food industry. These findings also indicated that the YGNGV-motif-based assay used in this study could identify novel class IIa bacteriocinogenic LAB, rapidly and specifically, saving time and labour by by-passing multiple separation and purification steps.
机译:在本研究中,开发并应用了基于YGNGV-motif的检测方法。鉴于对天然防腐剂的需求不断增长,我们着手获得能产生针对革兰氏阳性和革兰氏阴性细菌的细菌素的乳酸菌(LAB)。我们在这里从5种中国传统发酵食品中分离了123种LAB菌株,并使用琼脂孔扩散分析(AWDA)筛选了它们的细菌素生产。然后,为了获得产生LAB的IIa类细菌素的LAB,我们使用了基于YGNGV基元的检测方法,该方法基于14个简并引物,这些引物与目前存放在NCBI中的所有IIa类细菌素编码基因相匹配。 AWDA鉴定出的LAB菌株中有8种可以抑制革兰氏阳性和革兰氏阴性细菌。其中5个是YGNGV-amplicon阳性。在这5种分离物中,来自2个菌株(Y31和Y33)的扩增子与IIa类细菌素基因匹配。 Y31菌株在NCBI中表现出最高的抑制活性和与IIa类细菌素基因的最佳匹配,被鉴定为粪肠球菌。鸟肠球菌Y33的细菌素与肠球菌P的100%相同。这两种菌株均产生对单核细胞增生李斯特菌,大肠杆菌和枯草芽孢杆菌具有强大抗菌活性的细菌素,因此这些细菌素有望在食品工业中用作潜在的生物防腐剂。这些发现还表明,本研究中使用的基于YGNGV-motif的检测方法可以快速,准确地鉴定出新颖的IIa类细菌致癌LAB,通过绕开多个分离和纯化步骤,可以节省时间和精力。

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