Nanadoum Maoura
Laboratoire de Recherche sur les Substances Naturelles - Faculté des Sciences Exactes et Appliquées BP 1027 N’djaména Tchad
Mbailao Mbaiguinam
Laboratoire de Recherche sur les Substances Naturelles - Faculté des Sciences Exactes et Appliquées BP 1027 N’djaména Tchad
Huu Vang Nguyen
Laboratoire de Microbiologie et de Génétique Moléculaire. INA-PG INRA CBAI BP 01, 78 850 Thiverval Grignon France
Claude Gaillardin
Laboratoire de Microbiologie et de Génétique Moléculaire. INA-PG INRA CBAI BP 01, 78 850 Thiverval Grignon France
Jacques Pourquie
Laboratoire de Microbiologie et de Génétique Moléculaire. INA-PG INRA CBAI BP 01, 78 850 Thiverval Grignon France
Abstract
Seventy six yeast strains isolated form bili bili and others sample were identified and typed in purpose of selecting appropriate starter culture. Identification techniques included conventional phenetic method, PCR/RFLP of NTS2 rDNA region, partial sequencing of the D1/D2 region of 26S rDNA and karyotyping using contour clamped homogenous electric field (CHEF) technique. The Saccharomyces cereviseiae strains were also compared to industrial strains according to their fermentation profiles on maltose in the presence of 2- eoxy-D-glucose and to their karyotypes. We observed that the fermentation of bili bili was carried out by an indigenous natural flora predominantly represented by highly polymorphic S. cerevisiae strains whereas early steps in the process were carried out mainly by Kluyveromyces maxianus strains. All of the S. cerevisiae strains which were used in trial fermentation gave a good rate of fermentation suggesting that they may be used as starter cultures.
African Journal of Biotechnology Vol. 4 (7), pp. 646-656, 005