Buka Magwaza
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Buka Magwaza has a total of 3 co-authors. Here are the top co-authors by number of shared publications:
- Ayodeji Amobonye
Department of Polymer Chemistry and Technology Kaunas University of Technology Kaunas Lithuania
4 shared publications - Santhosh Pillai
Department of Biotechnology and Food Science, Faculty of Applied Sciences, Durban University of Technology, Durban, South Africa
4 shared publications - Prashant Bhagwat
Department of Biotechnology and Food Science, Faculty of Applied Sciences, Durban University of Technology, Durban, South Africa
3 shared publications
Latest Publications
- Open Access
- 6 November 2025
- Published by Elsevier in Scientific African
- Vol. 30
Comparative secretome dynamics of Beauveria bassiana under solid-state and submerged fermentation
- 6 November 2025
- Published by Elsevier in Scientific African
- Vol. 30
Open AccessComparative secretome dynamics of Beauveria bassiana under solid-state and submerged fermentation
- Open Access
- 19 June 2024
- Published by Springer Nature in Biomass Conversion and Biorefinery
- Vol. 15 (6) , 9753-9765
Hyper β-glucosidase producer Beauveria bassiana SAN01—optimization of fermentation conditions and evaluation of saccharification potential
The hyper-production of β-glucosidase by a local strain of Beauveria bassiana under submerged conditions is reported in this study. The initial screening of seven agricultural residues showed that the haulm of Bambara—an underutilized African legume—supported the highest β-glucosidase production; hence, statistical optimization of enzyme production was done using this biomass as the sole carbon source. Plackett–Burman design identified the concentrations of Bambara haulm, KCl, and NaCl as well as agitation speed and incubation time as the most significant factors affecting enzyme production. Subsequently, the central composite design predicted the optimal conditions (Bambara 57 g/L, KCl 302 mg/L, NaCl 154 mg/L, agitation speed 150 rpm, and incubation 223 h) for B. bassiana β-glucosidase production, which were further validated. The generated quadratic model was deemed significant judging from its F-value (201.63), adequate precision ratio (45.74), as well as the R 2 (0.9988), adjusted R 2 (0.9938), and predicted R 2 (0.9195) values. The optimization resulted in a ~5.36-fold increase in enzyme levels from the unoptimized production of ~133 to 711 U/mL. The enzyme was also demonstrated to efficiently hydrolyze cellobiose, converting more than 90% of the substrate to glucose. These results further establish the resourcefulness of the B. bassiana strain for the production of β-glucosidase enzyme, having immense potential, especially in the food and energy industries.
- 19 June 2024
- Published by Springer Nature in Biomass Conversion and Biorefinery
- Vol. 15 (6) , 9753-9765
Open AccessHyper β-glucosidase producer Beauveria bassiana SAN01—optimization of fermentation conditions and evaluation of saccharification potential
The hyper-production of β-glucosidase by a local strain of Beauveria bassiana under submerged conditions is reported in this study. The initial screening of seven agricultural residues showed that the haulm of Bambara—an underutilized African legume—supported the highest β-glucosidase production; hence, statistical optimization of enzyme production was done using this biomass as the sole carbon source. Plackett–Burman design identified the concentrations of Bambara haulm, KCl, and NaCl as well as agitation speed and incubation time as the most significant factors affecting enzyme production. Subsequently, the central composite design predicted the optimal conditions (Bambara 57 g/L, KCl 302 mg/L, NaCl 154 mg/L, agitation speed 150 rpm, and incubation 223 h) for B. bassiana β-glucosidase production, which were further validated. The generated quadratic model was deemed significant judging from its F-value (201.63), adequate precision ratio (45.74), as well as the R 2 (0.9988), adjusted R 2 (0.9938), and predicted R 2 (0.9195) values. The optimization resulted in a ~5.36-fold increase in enzyme levels from the unoptimized production of ~133 to 711 U/mL. The enzyme was also demonstrated to efficiently hydrolyze cellobiose, converting more than 90% of the substrate to glucose. These results further establish the resourcefulness of the B. bassiana strain for the production of β-glucosidase enzyme, having immense potential, especially in the food and energy industries.
- Top Cited PapersOpen Access
Microbial β-glucosidases: Recent advances and applications