L I I Ouoba1, C Parkouda, B Diawara, C Scotti, A H Varnam. 1. Microbiology Research Unit, Department of Health and Human Sciences, London Metropolitan University, London, UK. i.ouoba@londonmet.ac.uk
Abstract
AIMS: To identify Bacillus spp. responsible of the fermentation of Hibiscus sabdariffa for production of Bikalga, an alkaline fermented food used as a condiment in Burkina Faso. METHODS AND RESULTS: Seventy bacteria were isolated from Bikalga produced in different regions of Burkina Faso and identified by phenotyping and genotyping using PCR amplification of the 16S-23S rDNA intergenic transcribed spacer (ITS-PCR), repetitive sequence-based PCR (rep-PCR) and DNA sequencing. The isolates were characterized as motile, rod-shaped, endospore forming, catalase positive, Gram-positive bacteria. ITS-PCR allowed typing mainly at species level. Rep-PCR was more discriminative and allowed a typing at ssp. level. The DNA sequencing combined with the Blast search program and fermentation profiles using API 50CHB system allowed an identification of the bacteria as Bacillus subtilis, B. licheniformis, B. cereus, B. pumilus, B. badius, Brevibacillus bortelensis, B. sphaericus and B. fusiformis. B. subtilis were the predominant bacterium (42) followed by B. licheniformis (16). CONCLUSIONS: Various species and ssp. of Bacillus are involved in fermentation of H. sabdariffa for production of Bikalga. SIGNIFICANCE AND IMPACT OF THE STUDY: Selection of starter cultures of Bacillus for controlled production of Bikalga, selection of probiotic bacteria.
AIMS: To identify Bacillus spp. responsible of the fermentation of Hibiscus sabdariffa for production of Bikalga, an alkaline fermented food used as a condiment in Burkina Faso. METHODS AND RESULTS: Seventy bacteria were isolated from Bikalga produced in different regions of Burkina Faso and identified by phenotyping and genotyping using PCR amplification of the 16S-23S rDNA intergenic transcribed spacer (ITS-PCR), repetitive sequence-based PCR (rep-PCR) and DNA sequencing. The isolates were characterized as motile, rod-shaped, endospore forming, catalase positive, Gram-positive bacteria. ITS-PCR allowed typing mainly at species level. Rep-PCR was more discriminative and allowed a typing at ssp. level. The DNA sequencing combined with the Blast search program and fermentation profiles using API 50CHB system allowed an identification of the bacteria as Bacillus subtilis, B. licheniformis, B. cereus, B. pumilus, B. badius, Brevibacillus bortelensis, B. sphaericus and B. fusiformis. B. subtilis were the predominant bacterium (42) followed by B. licheniformis (16). CONCLUSIONS: Various species and ssp. of Bacillus are involved in fermentation of H. sabdariffa for production of Bikalga. SIGNIFICANCE AND IMPACT OF THE STUDY: Selection of starter cultures of Bacillus for controlled production of Bikalga, selection of probiotic bacteria.
Authors: Promiselynda Ijeoma Obioha; L Irene I Ouoba; Amarachukwu Anyogu; Brigitte Awamaria; Sarah Atchia; Philippa C Ojimelukwe; Jane P Sutherland; Hamid B Ghoddusi Journal: Braz J Microbiol Date: 2021-03-11 Impact factor: 2.476
Authors: Folarin A Oguntoyinbo; Vincenzina Fusco; Gyu-Sung Cho; Jan Kabisch; Horst Neve; Wilhelm Bockelmann; Melanie Huch; Lara Frommherz; Bernhard Trierweiler; Biserka Becker; Nabil Benomar; Antonio Gálvez; Hikmate Abriouel; Wilhelm H Holzapfel; Charles M A P Franz Journal: Front Microbiol Date: 2016-07-05 Impact factor: 5.640