高分辨率熔融分析在富含益生菌的食品基质中鉴定布拉氏酵母菌的潜力。

IF 2.7 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
BioTech Pub Date : 2024-11-14 DOI:10.3390/biotech13040048
Monika Borkowska, Michał Kułakowski, Kamila Myszka
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引用次数: 0

摘要

迄今为止,唯一有证据表明具有促进健康作用的益生菌酵母是布拉氏酵母菌。布拉氏酵母菌膳食补充剂和功能食品市场的扩大为食品掺假创造了有利环境,因此有必要进行快速检测以验证产品的益生菌状态。在此,对益生菌酵母的鉴定进行了 qPCR-HRM 分析测试。研究考察了引物对的有效性,该引物对设计用于扩增(a)以前设计用于鉴定食品衍生酵母的 rDNA 序列中的异质性区域和(b)与布拉氏酵母菌变种的生理和基因型差异相关的基因。通过对扩增子分化能力的初步测试,选出了 18SrRNA 和 ITS 的种间序列以及 HO、RPB2、HXT9 和 MAL11 的种属特异性序列。多片段 qPCR-HRM 分析足以进行依赖培养的布拉氏酵母菌鉴定,并被证明可有效鉴定膳食补充剂中的益生菌成分。利用更特异的基因内序列 HO 和 RPB2,成功鉴定了酸乳酒复杂微生物混合物中的布拉氏酵母菌。在测试的基质中,布拉氏酵母菌占主导地位,其数量与富含益生菌的食品相对应,这对利用 qPCR-HRM 分析进行鉴定至关重要。考虑到报告中的假设,qPCR-HRM 分析是验证富含益生菌食品的合适工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-Resolution Melting Analysis Potential for Saccharomyces cerevisiae var. boulardii Authentication in Probiotic-Enriched Food Matrices.

To date, the only probiotic yeast with evidence of health-promoting effects is Saccharomyces cerevisiae var. boulardii. The expanded market including dietary supplements and functional foods supplemented with Saccharomyces cerevisiae var. boulardii creates an environment conductive to food adulterations, necessitating rapid testing to verify product probiotic status. Herein, qPCR-HRM analysis was tested for probiotic yeast identification. The effectiveness of the primer pairs' set was examined, designed to amplify heterogeneous regions in (a) rDNA sequences previously designed to identify food-derived yeast and (b) genes associated with physiological and genotypic divergence of Saccharomyces cerevisiae var. boulardii. Preliminary tests of amplicons' differentiation power enabled the selection of interspecies sequences for 18SrRNA and ITS and genus-specific sequences HO, RPB2, HXT9 and MAL11. The multi-fragment qPCR-HRM analysis was sufficient for culture-dependent Saccharomyces cerevisiae var. boulardii identification and proved effective in the authentication of dietary supplements' probiotic composition. The identification of S. cerevisiae var. boulardii in complex microbial mixtures of kefir succeeded with more specific intragenus sequences HO and RPB2. The predominance of S. cerevisiae var. boulardii in the tested matrices, quantitatively corresponded to the probiotic-enriched food, was crucial for identification with qPCR-HRM analysis. Considering the reported assumptions, qPCR-HRM analysis is an appropriate tool for verifying probiotic-enriched food.

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来源期刊
BioTech
BioTech Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
3.70
自引率
0.00%
发文量
51
审稿时长
11 weeks
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