Arana-Sánchez A, Segura-García L E, Kirchmayr M, Orozco-Ávila I, Lugo-Cervantes E, Gschaedler-Mathis A
Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ), A.C., Av. Normalistas 800, CP 44270, Guadalajara, Jalisco, Mexico.
World J Microbiol Biotechnol. 2015 Feb;31(2):359-69. doi: 10.1007/s11274-014-1788-8. Epub 2015 Jan 8.
The process of cocoa fermentation is a very important step for the generation or aromatic compounds, which are attributable to the metabolism of the microorganisms involved. There are some reports about this process and the identification of microorganisms; however, there are no reports identifying the yeasts involved in a Mexican cocoa fermentation process using molecular biology techniques, including restricted fragment length polymorphism (RFLP) and denaturing gradient gel electrophoresis (DGGE). The aim of this study was to identify the main yeast species associated with Mexican cocoa fermentations employing culture-dependent and -independent techniques achieving two samplings with a 1 year time difference at the same site. Isolation of the microorganisms was performed in situ. Molecular identification of yeast isolates was achieved by RFLP analysis and rDNA sequencing. Total DNA from the microorganisms on the cocoa beans was utilized for the DGGE analysis. Bands from the DGGE gels were excised and sequenced. Nineteen isolated yeasts were identified (al specie level), three of which had never before been associated with cocoa fermentations worldwide. The detected predominant yeast varied from one technique to another. Hanseniaspora sp. resulted dominant in DGGE however Saccharomyces cerevisiae was the principal isolated species. In conclusion, the culture-dependent and -independent techniques complement each other showing differences in the main yeasts involved in spontaneous cocoa fermentation, probably due to the physiological states of the viable but non culturable yeasts. Furthermore important differences between the species detected in the two samplings were detected.
可可发酵过程是生成芳香化合物的非常重要的一步,这些化合物归因于所涉及微生物的代谢。关于这个过程以及微生物的鉴定已有一些报道;然而,尚无使用分子生物学技术(包括限制性片段长度多态性(RFLP)和变性梯度凝胶电泳(DGGE))鉴定参与墨西哥可可发酵过程的酵母的报道。本研究的目的是采用依赖培养和不依赖培养的技术,在同一地点进行两次时间间隔为1年的采样,以鉴定与墨西哥可可发酵相关的主要酵母种类。微生物的分离在原位进行。通过RFLP分析和rDNA测序对酵母分离株进行分子鉴定。利用可可豆上微生物的总DNA进行DGGE分析。从DGGE凝胶上切下条带并进行测序。鉴定出19种分离酵母(在种水平),其中3种在全球范围内从未与可可发酵相关联。检测到的优势酵母因技术不同而有所差异。汉逊酵母属在DGGE中占主导地位,然而酿酒酵母是主要的分离物种。总之,依赖培养和不依赖培养的技术相互补充,显示出自发可可发酵中主要酵母的差异,这可能是由于活的但不可培养酵母的生理状态所致。此外,在两次采样中检测到的物种之间存在重要差异。