PMID- 17161485 OWN - NLM STAT- MEDLINE DCOM- 20070514 LR - 20070219 IS - 0168-1605 (Print) IS - 0168-1605 (Linking) VI - 114 IP - 2 DP - 2007 Mar 10 TI - The microbiology of Ghanaian cocoa fermentations analysed using culture-dependent and culture-independent methods. PG - 168-86 AB - Export of cocoa beans is of great economic importance in Ghana and several other tropical countries. Raw cocoa has an astringent unpleasant taste and a spontaneous fermentation is the first step in a process leading to cocoa beans with the characteristic cocoa flavour and taste. The microbiology of Ghanaian cocoa fermentations was investigated using culture-dependent and culture-independent methods. Samples were collected at 12 hour intervals during 96-144 hour tray and traditional heap fermentations. Yeast, Lactic Acid Bacteria (LAB), Acetic Acid Bacteria (AAB) and Bacillus spp. were enumerated on suitable substrates and identified using phenotypic and molecular methods. The yeast and bacterial micro-populations involved in the cocoa fermentation were further investigated using the culture-independent method Denaturing Gradient Gel Electrophopresis (DGGE). A microbiological succession was observed during the fermentations. At the onset of fermentation yeasts were the dominating microorganisms. Lactic Acid Bacteria became dominant after 12-24 h of fermentation and remained predominant throughout the fermentations with AAB reaching high counts in the mid phase of fermentation. Bacillus spp. were only detected during heap fermentations where they reached high numbers during the later stages of fermentation. Hanseniaspora guilliermondii was the predominant yeast during the initial phase and Pichia membranifaciens during the later phases of fermentation. A number of other yeast species including three putatively undescribed species were isolated during the fermentations. Lactobacillus fermentum was the dominant LAB in most samples. Several other LAB including Lactobacillus plantarum, Leuconostoc pseudomesenteroides, Leuconostoc pseudoficulneum, Pediocococcus acidilactici and a putatively undescribed LAB species were detected during the fermentations. Acetobacter syzygii, Acetobacter pasteurianus and Acetobacter tropicalis were the predominant AAB in all investigated fermentations. During the later stages of heap fermentation Bacillus licheniformis and occasionally other Bacillus spp. were detected in high numbers. In general the culture-based findings were confirmed using DGGE. However, DGGE indicated that Lc. pseudoficulneum plays a more important role during the fermentation of cocoa than expected from the culture-based findings as it yielded a strong band in most DGGE fingerprints. Cluster analysis of the DGGE fingerprints revealed that the DGGE fingerprints clustered according to fermentation site. Within each fermentation site the profiles clustered according to fermentation time. The DGGE method seems to offer a relatively fast and reliable tool for studying yeast and bacterial dynamics during cocoa fermentations. FAU - Nielsen, D S AU - Nielsen DS AD - Department of Food Science, Food Microbiology, Center for Advanced Food Studies (LMC), Royal Veterinary and Agricultural University, Frederiksberg, Denmark. dn@kvl.dk FAU - Teniola, O D AU - Teniola OD FAU - Ban-Koffi, L AU - Ban-Koffi L FAU - Owusu, M AU - Owusu M FAU - Andersson, T S AU - Andersson TS FAU - Holzapfel, W H AU - Holzapfel WH LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20061208 PL - Netherlands TA - Int J Food Microbiol JT - International journal of food microbiology JID - 8412849 SB - IM MH - Bacteria/classification/*growth & development/isolation & purification MH - Cacao/*microbiology MH - Cluster Analysis MH - Colony Count, Microbial/methods MH - Electrophoresis, Polyacrylamide Gel/methods MH - *Fermentation MH - *Food Microbiology MH - Ghana MH - Kinetics MH - Population Dynamics MH - Species Specificity MH - Yeasts/classification/*growth & development/isolation & purification EDAT- 2006/12/13 09:00 MHDA- 2007/05/15 09:00 CRDT- 2006/12/13 09:00 PHST- 2006/03/27 00:00 [received] PHST- 2006/07/14 00:00 [revised] PHST- 2006/09/15 00:00 [accepted] PHST- 2006/12/13 09:00 [pubmed] PHST- 2007/05/15 09:00 [medline] PHST- 2006/12/13 09:00 [entrez] AID - S0168-1605(06)00520-4 [pii] AID - 10.1016/j.ijfoodmicro.2006.09.010 [doi] PST - ppublish SO - Int J Food Microbiol. 2007 Mar 10;114(2):168-86. doi: 10.1016/j.ijfoodmicro.2006.09.010. Epub 2006 Dec 8.