| Literature DB >> 35713813 |
Atim Asitok1,2, Maurice Ekpenyong3,4, Iquo Takon5, Sylvester Antai1,2, Nkpa Ogarekpe6, Richard Antigha6, Philomena Edet1, Agnes Antai7, Joseph Essien8.
Abstract
Bacterial alkaline peptidases, especially from Bacillus species, occupy the frontline in global enzyme market, albeit with poor production economics. Here, we report the deployment of response surface methodology approximations to optimize fermentation parameters for enhanced yield of alkaline peptidase by the non-Bacillus bacterium; Stenotrophomonas acidaminiphila. Shake flask production under optimized conditions was scaled up in a 5-L bench-scale bioreactor. Logistic and modified Gompertz models revealed significant fits for biomass formation, total protein, and substrate consumption models. Maximum specific growth rate (µmax = 0.362 h-1) of the bacterium in the optimized medium did not differ significantly from those in Luria-Bertani and trypticase soy broths. The aqueous two-phase system-purified 45.7 kDa alkaline protease retained 83% activity which improved with increasing sodium dodecyl sulfate concentration thus highlighting potential laundry application. Maximum enzyme activity occurred at 75ºC and pH 10.5 but was inhibited by 5 mM phenyl-methyl-sulfonyl fluoride suggesting a serine-protease nature.Entities:
Keywords: Alkaline peptidase; Kinetic modeling; Response surface optimization; Stenotrophomonas acidaminiphila; Sustainable environmental pollution abatement
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Year: 2022 PMID: 35713813 DOI: 10.1007/s00203-022-03010-9
Source DB: PubMed Journal: Arch Microbiol ISSN: 0302-8933 Impact factor: 2.552