ENOLAB, ERI-ISIC BioTecMed/ViSoCa, Universitat de València, Burjassot 46100, Valencia, Spain.
ENOLAB, ERI-ISIC BioTecMed/ViSoCa, Universitat de València, Burjassot 46100, Valencia, Spain.
Int J Food Microbiol. 2017 Nov 16;261:25-34. doi: 10.1016/j.ijfoodmicro.2017.08.019. Epub 2017 Sep 4.
A novel quantitative PCR assay called Cells-qPCR has been developed for the rapid detection and quantification of yeasts, lactic acid bacteria (LAB) and acetic acid bacteria (AAB) directly from grape must and wine that does not require DNA extraction. The assay was tested on Brettanomyces bruxellensis, Saccharomyces cerevisiae, Lactobacillus plantarum, Oenococcus oeni, Acetobacter aceti and Gluconobacter oxydans in culture media, and in white and red grape musts and wines. Standard curves were constructed from DNA and cells for the six target species in all the matrices. Good efficiencies were obtained for both when comparing DNA and cells standard curves. No reaction inhibition was observed between matrices for each species. Cells quantification was linear over a range of cell concentrations (7, 5 or 4 orders of magnitude) and detected as few as one cell per reaction in all the matrices. The developed Cells-qPCR assay is a robust, reliable, fast and specific method to detect and quantify different yeasts, LAB and AAB species in grape must and wine that avoids DNA extraction and overcomes the presence of inhibitors like polyphenols and ethanol.
一种新型的定量 PCR 检测方法称为 Cells-qPCR,用于快速检测和定量葡萄汁和葡萄酒中的酵母、乳酸菌(LAB)和醋酸菌(AAB),无需提取 DNA。该检测方法在培养基中以及白葡萄汁和葡萄酒、红葡萄汁和葡萄酒中对布鲁塞尔酵母(Brettanomyces bruxellensis)、酿酒酵母(Saccharomyces cerevisiae)、植物乳杆菌(Lactobacillus plantarum)、奥尼克氏菌(Oenococcus oeni)、醋化醋杆菌(Acetobacter aceti)和氧化葡萄糖酸杆菌(Gluconobacter oxydans)进行了测试。在所有基质中,针对六个目标物种,均从 DNA 和细胞构建了标准曲线。比较 DNA 和细胞标准曲线时,均获得了良好的效率。对于每个物种,不同基质之间均未观察到反应抑制。在所有基质中,细胞定量在细胞浓度(7、5 或 4 个数量级)范围内呈线性,每个反应检测到的细胞数量少至一个。开发的 Cells-qPCR 检测方法是一种强大、可靠、快速和特异性的方法,可用于检测和定量葡萄汁和葡萄酒中的不同酵母、乳酸菌和醋酸菌,避免了 DNA 提取,并克服了多酚和乙醇等抑制剂的存在。