Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013:2013:103960.
doi: 10.1155/2013/103960. Epub 2013 Feb 26.

Production of Enzymes from Agroindustrial Wastes by Biosurfactant-Producing Strains of Bacillus subtilis

Affiliations

Production of Enzymes from Agroindustrial Wastes by Biosurfactant-Producing Strains of Bacillus subtilis

Francisco Fábio Cavalcante Barros et al. Biotechnol Res Int. 2013.

Abstract

Bacteria in the genus Bacillus are the source of several enzymes of current industrial interest. Hydrolases, such as amylases, proteases, and lipases, are the main enzymes consumed worldwide and have applications in a wide range of products and industrial processes. Fermentation processes by Bacillus subtilis using cassava wastewater as a substrate are reported in the technical literature; however, the same combination of microorganisms and this culture medium is limited or nonexistent. In this paper, the amylase, protease, and lipase production of ten Bacillus subtilis strains previously identified as biosurfactant producers in cassava wastewater was evaluated. The LB1a and LB5a strains were selected for analysis using a synthetic medium and cassava wastewater and were identified as good enzyme producers, especially of amylases and proteases. In addition, the enzymatic activity results indicate that cassava wastewater was better than the synthetic medium for the induction of these enzymes.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Average halo diameter in plates for LB1a and LB5a Bacillus subtilis strains: (a) amylase, (b) protease, and (c) lipase.
Figure 2
Figure 2
Milk agar plates after 24 h (a) and 72 h (b) inoculated with Bacillus subtilis strains LB117 and LB1a (a) and LB5a and ATCC21332 (b); the proteolysis halos are evident.
Figure 3
Figure 3
Enzymatic activity kinetics of LB5a and LB1a strains in a synthetic medium supplemented: (a) amylase, (b) protease, and (c) lipase.
Figure 4
Figure 4
Enzymatic activity kinetics of LB5a and LB1a strains grown in glass flasks using cassava wastewater as culture medium: (a) amylase, (b) protease, and (c) lipase.
Figure 5
Figure 5
Enzymatic activity kinetics of LB5a and LB1a strains grown in bioreactor using cassava wastewater as culture medium: (a) amylase, (b) protease, and (c) lipase.

References

    1. Schallmey M, Singh A, Ward OP. Developments in the use of Bacillus species for industrial production. Canadian Journal of Microbiology. 2004;50(1):1–17. - PubMed
    1. Kunst F, Rapoport G. Salt stress is an environmental signal affecting degradative enzyme synthesis in Bacillus subtilis . Journal of Bacteriology. 1995;177(9):2403–2407. - PMC - PubMed
    1. Konsoula Z, Liakopoulou-Kyriakides M. Co-production of α-amylase and β-galactosidase by Bacillus subtilis in complex organic substrates. Bioresource Technology. 2007;98(1):150–157. - PubMed
    1. Syu MJ, Chen YH. A study on the α-amylase fermentation performed by Bacillus amyloliquefaciens . Chemical Engineering Journal. 1997;65(3):237–247.
    1. Pandey A, Nigam P, Soccol CR, Soccol VT, Singh D, Mohan R. Advances in microbial amylases. Biotechnology and Applied Biochemistry. 2000;31(2):135–152. - PubMed