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Rapid molecular methods for enumeration and taxonomical identification of acetic acid bacteria responsible for submerged vinegar production

机译:快速的分子方法,用于枚举和分类识别醋产生的醋菌

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The aim of the present study was to search for a rapid and reliable method to enumerate viable acetic acid bacteria (AAB) and to identify to genera and species level AAB isolates from vinegars in full acetic fermentation elaborated by the submerged method from cider, wine and spirit ethanol in industrial bioreactors. Results showed that the rapid epifluorescence staining method using the LIVE/DEAD BacLight bacterial viability kit and direct counts in Neubauer chamber rendered consistent and reliable data for viable cell counts of bacteria in all the studied vinegars. A linear correlation was shown between viable cell counts and fermentation rates. The highest fermentation rates and viable cell counts were found in cider vinegars, whereas spirit vinegars showed the lowest values for both parameters. Eighty-four AAB pure isolates were recovered from 41 different vinegar samples and were submitted to DNA extraction. PCR amplification of the 16S–23S intergenic spacer region of rDNA and subsequent sequencing were carried out to identify isolates to species level. Results showed that Gluconacetobacter europaeus was the predominant cultivable species, appearing in 79% of the total isolates. This was the unique species found in spirit vinegars, and this is the first time that AAB from spirit vinegars are taxonomically identified. Ga. europaeus was as well the predominant cultivable species in white wine vinegars. Cider vinegars presented the highest variability of species: Ga. europaeus (35.3% appearance among cultivable isolates), Ga. xylinus (35.3%), Acetobacter pasteurianus (17.6%) and Ga. hansenii (11.8%). Red wine vinegars showed cultivable isolates of the species Ga. xylinus (71.4%) and Ga. europaeus (28.6%). Summarising, both described methods for AAB enumeration and taxonomical identification proved to be fast and reliable methods, and results revealed Ga. europaeus as the cultivable major species in vinegars in full fermentation conducted by the submerged method, suggesting that Ga. europaeus strains can constitute excellent starter cultures for the elaboration of vinegars by the submerged method.
机译:本研究的目的是寻找一种快速可靠的方法来枚举可行的乙酸细菌(AAB),并鉴定通过醋浸法从苹果酒,葡萄酒和葡萄酒中精制而成的全乙酸发酵中醋的属和种水平AAB分离株。工业生物反应器中的酒精乙醇。结果表明,使用LIVE / DEAD BacLight细菌生存力试剂盒进行快速的快速荧光染色方法以及在Neubauer箱中进行直接计数可为所有研究的醋中细菌的活细胞计数提供一致且可靠的数据。活细胞计数和发酵速率之间显示线性相关性。苹果醋中发酵率和活细胞数最高,而烈酒中两个参数的最低。从41种不同的醋样品中回收了84种AAB纯分离株,并进行了DNA提取。对rDNA的16S–23S基因间隔区进行PCR扩增并进行后续测序,以鉴定分离到物种水平的分离株。结果表明,欧洲葡糖杆菌是可培养的主要菌种,占总分离株的79%。这是在白酒醋中发现的独特物种,这是首次从分类学上鉴定白酒中的AAB。在白葡萄酒醋中,Ga.europaeus也是主要的可栽培物种。苹果酒醋具有最大的变异性:欧洲油菜(Ga.europaeus)(在可分离的菌株中占35.3%),木霉油(Gas xylinus)(35.3%),巴氏醋杆菌(17.6%)和汉森油菜(11.8%)。红酒醋显示出可栽培的木霉菌(Gax xylinus)(71.4%)和欧洲油菜(Ga.europaeus)(28.6%)。综上所述,用于AAB枚举和分类学鉴定的两种描述方法均被证明是快速可靠的方法,结果表明,通过浸没法进行完全发酵后,欧洲油菜是醋中可培养的主要菌种,表明欧洲油菜菌株可以构成优良的菌株。用浸没法精制醋的发酵剂。

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