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Rapid investigation of French sourdough microbiota by restriction fragment length polymorphism of the 16S-23S rRNA gene intergenic spacer region

机译:通过16S-23S rRNA基因间间隔区的限制性片段长度多态性快速研究法国酵母菌

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摘要

The aim of the present research is to identify rapidly the lactic acid bacteria (LAB) microflora of four natural French sourdoughs (GO, BF, VB and RF), applying a biphasic (restriction length polymorphism (RFLP) and sequencing) approach for bacterial identification. For this purpose, a database with the RFLP patterns of 30 lactobacilli type strains was created. So-developed ISR-RFLP algorithm was further applied for the differentiation and identification of 134 sourdough isolates. The 16S-23S rDNA intergenic spacer region was amplified by primers tAla and 23S/10, and then digested by HindIII, HinfI and l-TaqI enzymes. Nucleotide sequences of the cloned 16S-23S intergenic spacer region (ISR) were determined by the dideoxynucleotide chain termination method. The T7Prom and M13rev primers flanking the multiple cloning site of pCR2.1 DNA were used to sequence both DNA strands. The RFLP profile obtained upon digestion with HindIII, HinfI and l-TaqI enzymes can be used to discriminate Lactobacillus sanfranciscensis (66%), Lactobacillus panis (17%), Lactobacillus nantensis (11%) and Lactobacillus hammesii(6%) in sourdough GO, Lactobacillus sanfranciscensis (80%), Lactobacillus spicheri (14%) and Lactobacillus pontis(6%) in sourdoughs BF. In sourdoughs VB, which differed in the process temperature, we can differentiate Lactobacillus sanfranciscensis (89%) and Leuconostoc mesenteroidessubsp. mesenteroides (11%). Lactobacillus frumenti(47%), Lactobacillus hammesii (8%), and Lactobacillus paralimentarius (45%) were differentiated in sourdough RF.
机译:本研究的目的是快速鉴定四种法国天然酵母(GO,BF,VB和RF)的乳酸菌(LAB)微生物区系,采用双相(限制性长度多态性(RFLP)和测序)方法进行细菌鉴定。为此,创建了具有30个乳杆菌型菌株RFLP模式的数据库。如此开发的ISR-RFLP算法被进一步用于134种酵母菌的鉴别和鉴定。用引物tAla和23S / 10扩增16S-23S rDNA基因间隔区,然后用HindIII,HinfI和1-TaqI酶消化。通过双脱氧核苷酸链终止法确定克隆的16S-23S基因间隔区(ISR)的核苷酸序列。在pCR2.1 DNA的多个克隆位点两侧的T7Prom和M13rev引物用于对两条DNA链进行测序。用HindIII,HinfI和l-TaqI酶消化后获得的RFLP谱可用于区分酸GO中的旧金山乳杆菌(66%),潘氏乳杆菌(17%),南乳杆菌(11%)和汉姆氏乳杆菌(6%) ,酸面团高炉中的Sanfranciscensis乳杆菌(80%),spicheri乳杆菌(14%)和pontis乳杆菌(6%)。在过程温度不同的酸面团VB中,我们可以区分乳杆菌Sanfranciscensis(89%)和中间肠球菌Leuconostoc mesenteroidessubsp。 mesenteroides(11%)。在发酸RF中区分了富勒氏乳杆菌(47%),哈密斯乳杆菌(8%)和副乳杆菌(45%)。

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