Starter culture evaluation for the production of ugba from African oil bean seed Pentaclethra macrophylla

Ugba was prepared in the laboratory by the traditional method from the African oil bean seeds Pentaclethra macrophylla. Microorganisms were isolated from the fermenting slices of the beans at 24 h intervals for 5 days and characterised. The results show that only bacteria were isolated from the bean...

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Bibliographic Details
Published inJournal of the science of food and agriculture Vol. 77; no. 1; pp. 127 - 132
Main Authors Mbajunwa, O.K, Akingbala, J.O, Mulongoy, K, Oguntimein, G
Format Journal Article
LanguageEnglish
Published London John Wiley & Sons, Ltd 01.05.1998
Wiley
Published for the Society of Chemical Industry by Elsevier Applied Science
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Summary:Ugba was prepared in the laboratory by the traditional method from the African oil bean seeds Pentaclethra macrophylla. Microorganisms were isolated from the fermenting slices of the beans at 24 h intervals for 5 days and characterised. The results show that only bacteria were isolated from the bean slices. Fungi and yeasts were not isolated. The bacterial isolates were identified as Bacillus subtilis, Bacillus cereus, Pseudomonas chlororaphis, Micrococcus roseus and Staphylococci saprophyticus. The identified bacterial isolates were evaluated for their ability to ferment the cooked oil bean slices into ugba with its desirable quality characteristics of colour, texture, aroma and overall acceptability. Bacillus subtilis was significantly (P < 0.05) more active in fermenting the oil bean than the other isolates. Pseudomonas chlororaphis fermented the oil bean actively but caused greening of the slices probably due to the production of the green chloraphin pigment. Staphylococcus saprophyticus, M roseus and B cereus appeared unimportant in the fermentation and may be contaminants. Bacillus subtilis was therefore selected as the single starter culture for ugba production.
Bibliography:ark:/67375/WNG-KHG58BS5-K
istex:9101469005172FB804C4946310D06A9864501462
ArticleID:JSFA17
ISSN:0022-5142
1097-0010
DOI:10.1002/(SICI)1097-0010(199805)77:1<127::AID-JSFA17>3.0.CO;2-4