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本文引用的文献

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Rapid Detection and Identification of Lactobacillus spp. in Dairy Products by Using the Polymerase Chain Reaction.利用聚合酶链反应快速检测和鉴定乳制品中的乳酸杆菌属
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Bifidobacterial diversity in human feces detected by genus-specific PCR and denaturing gradient gel electrophoresis.通过属特异性聚合酶链反应和变性梯度凝胶电泳检测人类粪便中的双歧杆菌多样性。
Appl Environ Microbiol. 2001 Feb;67(2):504-13. doi: 10.1128/AEM.67.2.504-513.2001.
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Bifidobacterium lactis Meile et al. 1997 is a subjective synonym of Bifidobacterium animalis (Mitsuoka 1969) Scardovi and Trovatelli 1974.乳酸双歧杆菌(Meile等人,1997年)是动物双歧杆菌(Mitsuoka,1969年)斯卡多维和特罗瓦泰利1974年的主观同物异名。
Microbiol Immunol. 2000;44(10):815-20. doi: 10.1111/j.1348-0421.2000.tb02568.x.
4
S-layer gene as a molecular marker for identification of Lactobacillus helveticus.表层蛋白基因作为瑞士乳杆菌鉴定的分子标记。
FEMS Microbiol Lett. 2000 Aug 15;189(2):275-9. doi: 10.1111/j.1574-6968.2000.tb09243.x.
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Multiplex PCR for the detection of Lactobacillus pontis and two related species in a sourdough fermentation.用于检测酸面团发酵中 Pontis 乳杆菌及两个相关物种的多重聚合酶链反应
Appl Environ Microbiol. 2000 May;66(5):2113-6. doi: 10.1128/AEM.66.5.2113-2116.2000.
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Distribution of bifidobacterial species in human intestinal microflora examined with 16S rRNA-gene-targeted species-specific primers.使用靶向16S rRNA基因的种特异性引物检测人类肠道微生物群中双歧杆菌的分布。
Appl Environ Microbiol. 1999 Oct;65(10):4506-12. doi: 10.1128/AEM.65.10.4506-4512.1999.
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Rapid identification of human intestinal bifidobacteria by 16S rRNA-targeted species- and group-specific primers.利用靶向16S rRNA的种属特异性引物快速鉴定人肠道双歧杆菌
FEMS Microbiol Lett. 1998 Oct 15;167(2):113-21. doi: 10.1111/j.1574-6968.1998.tb13216.x.
8
Evaluation of using a short region of the recA gene for rapid and sensitive speciation of dominant bifidobacteria in the human large intestine.利用recA基因短区域对人类大肠中优势双歧杆菌进行快速灵敏的物种鉴定的评估。
FEMS Microbiol Lett. 1997 Sep 15;154(2):377-83. doi: 10.1111/j.1574-6968.1997.tb12670.x.
9
Identification and quantification of Bifidobacterium species isolated from food with genus-specific 16S rRNA-targeted probes by colony hybridization and PCR.通过菌落杂交和聚合酶链反应,使用属特异性16S rRNA靶向探针鉴定和定量从食品中分离出的双歧杆菌属菌种。
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10
Development of oligonucleotide primers from the 16S-23S rRNA intergenic sequences for identifying different dairy and probiotic lactic acid bacteria by PCR.基于16S - 23S rRNA基因间隔序列开发寡核苷酸引物,用于通过聚合酶链反应(PCR)鉴定不同的乳制品和益生菌乳酸菌。
Int J Food Microbiol. 1997 Mar 18;35(1):49-56. doi: 10.1016/s0168-1605(97)88066-x.

通过联合多重聚合酶链反应方法对不同环境分离株中的乳酸双歧杆菌进行特异性鉴定和靶向表征。

Specific identification and targeted characterization of Bifidobacterium lactis from different environmental isolates by a combined multiplex-PCR approach.

作者信息

Ventura M, Reniero R, Zink R

机构信息

Nestlé Research Center, Vers-Chez-Les-Blanc, 1000 Lausanne 26, Switzerland.

出版信息

Appl Environ Microbiol. 2001 Jun;67(6):2760-5. doi: 10.1128/AEM.67.6.2760-2765.2001.

DOI:10.1128/AEM.67.6.2760-2765.2001
PMID:11375192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC92936/
Abstract

The species Bifidobacterium lactis, with its main representative strain Bb12 (DSM 10140), is a yoghurt isolate used as a probiotic strain and is commercially applied in different types of yoghurts and infant formulas. In order to ensure the genetic identity and safety of this bacterial isolate, species- and strain-specific molecular tools for genetic fingerprinting must be available to identify isolated bifidobacteria or lactic acid bacteria from, e.g., various clinical environments of relevance in medical microbiology. Two opposing rRNA gene-targeted primers have been developed for specific detection of this microorganism by PCR. The specificity of this approach was evaluated and verified with DNA samples isolated from single and mixed cultures of bifidobacteria and lactobacilli (48 isolates, including the type strains of 29 Bifidobacterium and 9 Lactobacillus species). Furthermore, we performed a Multiplex-PCR using oligonucleotide primers targeting a specific region of the 16S rRNA gene for the genus Bifidobacterium and a conserved eubacterial 16S rDNA sequence. The specificity and sensitivity of this detection with a pure culture of B. lactis were, respectively, 100 bacteria/ml after 25 cycles of PCR and 1 to 10 bacteria/ml after a 50-cycle nested-PCR approach.

摘要

乳酸双歧杆菌及其主要代表性菌株Bb12(DSM 10140)是一种从酸奶中分离得到的益生菌菌株,已被商业化应用于不同类型的酸奶和婴儿配方奶粉中。为确保该分离菌株的基因一致性和安全性,必须具备物种和菌株特异性的基因指纹分析分子工具,以便从例如医学微生物学中各种相关临床环境中鉴定分离出的双歧杆菌或乳酸菌。已经开发了两种针对rRNA基因的反向引物,用于通过PCR特异性检测这种微生物。使用从双歧杆菌和乳酸菌的单一及混合培养物中分离的DNA样本(48个分离株,包括29种双歧杆菌和9种乳酸菌的模式菌株)对该方法的特异性进行了评估和验证。此外,我们使用针对双歧杆菌属16S rRNA基因特定区域的寡核苷酸引物和保守的真细菌16S rDNA序列进行了多重PCR。用乳酸双歧杆菌纯培养物进行该检测的特异性和灵敏度,在PCR 25个循环后分别为每毫升100个细菌,在50个循环的巢式PCR方法后为每毫升1至10个细菌。