Research Group of Industrial Microbiology and Food Biotechnology (IMDO), Faculty of Sciences and Bio-Engineering Sciences, Vrije Universiteit Brussel (VUB), Pleinlaan 2, B-1050 Brussels, Belgium.
Food Microbiol. 2011 May;28(3):457-64. doi: 10.1016/j.fm.2010.10.010. Epub 2010 Oct 27.
To speed up research on the usefulness and selection of bacterial starter cultures for cocoa bean fermentation, a benchmark cocoa bean fermentation process under natural fermentation conditions was developed successfully. Therefore, spontaneous fermentations of cocoa pulp-bean mass in vessels on a 20 kg scale were tried out in triplicate. The community dynamics and kinetics of these fermentations were studied through a multiphasic approach. Microbiological analysis revealed a limited bacterial species diversity and targeted community dynamics of both lactic acid bacteria (LAB) and acetic acid bacteria (AAB) during fermentation, as was the case during cocoa bean fermentations processes carried out in the field. LAB isolates belonged to two main (GTG)(5)-PCR clusters, namely Lactobacillus plantarum and Lactobacillus fermentum, with Fructobacillus pseudofilculneus occurring occasionally; one main (GTG)(5)-PCR cluster, composed of Acetobacter pasteurianus, was found among the AAB isolates, besides minor clusters of Acetobacter ghanensis and Acetobacter senegalensis. 16S rRNA-PCR-DGGE revealed that L. plantarum and L. fermentum dominated the fermentations from day two until the end and Acetobacter was the only AAB species present at the end of the fermentations. Also, species of Tatumella and Pantoea were detected culture-independently at the beginning of the fermentations. Further, it was shown through metabolite target analyses that similar substrate consumption and metabolite production kinetics occurred in the vessels compared to spontaneous cocoa bean fermentation processes. Current drawbacks of the vessel fermentations encompassed an insufficient mixing of the cocoa pulp-bean mass and retarded yeast growth.
为了加快对可可豆发酵用细菌发酵剂的有用性和选择的研究,成功开发了一种在自然发酵条件下的基准可可豆发酵工艺。因此,在 20 公斤规模的容器中尝试了三次自发的可可果肉-豆粕发酵。通过多相方法研究了这些发酵的群落动态和动力学。微生物分析显示,在发酵过程中,无论是乳酸菌(LAB)还是醋酸菌(AAB),细菌的物种多样性和靶向群落动态都受到限制,这与在野外进行的可可豆发酵过程中情况相同。LAB 分离株属于两个主要的(GTG)(5)-PCR 簇,即植物乳杆菌和发酵乳杆菌,偶尔出现假纤维果糖杆菌;在 AAB 分离株中发现了一个主要的(GTG)(5)-PCR 簇,由巴氏醋酸杆菌组成,此外还有少数的阿克曼氏醋酸杆菌和塞内加尔醋酸杆菌。16S rRNA-PCR-DGGE 显示,植物乳杆菌和发酵乳杆菌从第二天到发酵结束一直占主导地位,醋酸菌是发酵结束时唯一存在的 AAB 物种。此外,在发酵开始时,还独立地从培养物中检测到塔图姆菌和潘氏菌。此外,通过代谢物目标分析表明,在容器中与自发的可可豆发酵过程相比,发生了相似的基质消耗和代谢产物生成动力学。目前容器发酵的缺点包括可可果肉-豆粕的混合不充分和酵母生长迟缓。