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1.
Lett Appl Microbiol ; 67(4): 354-362, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29947432

ABSTRACT

Analysis of the bacterial community dynamics during the production of traditional fermented condiments is important for food safety assessment, quality control and development of starter culture technology. In this study, bacteria isolated during the processing of iru and ogiri, two commonly consumed condiments in Nigeria, were characterized based on phylogenetic analyses of the bacterial 16S rRNA gene. A total of 227 isolates were obtained and clustered into 12 operational taxonomic units (OTUs) based on 97% 16S rRNA gene similarity. The OTUs spanned three phyla (Firmicutes, Actinobacteria and Proteobacteria), and nine genera: Acinetobacter, Aerococcus, Bacillus, Enterococcus, Enterobacter, Lysinibacillus, Micrococcus, Proteus and Staphylococcus. OTUs closely related to species of Bacillus dominated the processing stages of both condiments. Although no single OTU occurred throughout iru processing stages, an OTU (mostly related to B. safensis) dominated the ogiri processing stages indicating potentials for the development of starter culture. However, other isolates such as those of Enterococcus spp. and Lysinibacillus spp. may be potential starters for iru fermentation. Presumptive food-borne pathogens were also detected at some stages of the condiments' processing, possibly due to poor hygienic practices. SIGNIFICANCE AND IMPACT OF THE STUDY: Iru and ogiri are important condiments used for flavour enhancement in foods and serve as protein substitutes in diets among rural populations across West Africa. Consumption of these condiments is growing, reinforcing the need to scale up their production. Production of these condiments includes spontaneous fermentation, which often leads to inconsistent product quality and unguaranteed safety. This study has demonstrated the bacterial succession in iru and ogiri processing and highlights species that could be selected and exploited for starter culture development. This study provides a starting point to produce quality and microbiologically safe iru and ogiri condiments.


Subject(s)
Actinobacteria/metabolism , Condiments/microbiology , Fermented Foods/microbiology , Firmicutes/metabolism , Proteobacteria/metabolism , Actinobacteria/classification , Actinobacteria/genetics , Bacillus/classification , Bacillus/genetics , Bacillus/metabolism , Fermentation , Firmicutes/classification , Firmicutes/genetics , Food Safety , Nigeria , Phylogeny , Proteobacteria/classification , Proteobacteria/genetics , RNA, Ribosomal, 16S/genetics , Seeds/metabolism
2.
Food Microbiol ; 24(6): 571-6, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17418307

ABSTRACT

Saccharomyces cerevisiae, Candida krusei, C. tropicalis, Geotrichum candidum, G. fermentans and Rhodotorula graminis were isolated during the fermentation of maize for ogi production. All the isolates except Geotrichum fermentans and Rhodotorula graminis were able to degrade phytate. All the yeasts strains exhibited lipase and esterase activities. Only S. cerevisiae (2.60%) and C. krusei (7.41%) exhibited amylase activities. Candida sp. produced wider zone of inhibition than the other yeasts strains tested during lipase activity while S. cerevisiae strains produced significantly wider zone of clearing as compared to the other yeasts for esterase activities. The study of inter-relationships between Lactobacillus plantarum and yeasts (C. krusei and S. cerevisiae) showed that the growth of the yeast strains were enhanced during fermentation by the presence of the lactic acid bacteria, but the growth of the L. plantarum strain was significantly enhanced especially by the C. krusei.


Subject(s)
Fermentation , Food Microbiology , Yeasts/enzymology , Yeasts/growth & development , Zea mays/microbiology , Amylases/metabolism , Candida/classification , Candida/enzymology , Candida/growth & development , Esterases/metabolism , Hydrogen-Ion Concentration , Lipase/metabolism , Phylogeny , Phytic Acid/metabolism , Saccharomyces cerevisiae/classification , Saccharomyces cerevisiae/enzymology , Saccharomyces cerevisiae/growth & development , Species Specificity , Time Factors , Yeasts/classification
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