Abstract
The enzymatic activities occurring on painted walls in a tropical environment have become critical given the rate of aesthetic biodeterioration of such walls. Pigmented heterotrophic microorganisms isolated from discolored painted walls in Lagos, Nigeria were screened for their phosphatase activities. The strains were characterized by morphological methods and 16S rDNA analysis as belonging to the genera Aspergillus, Meyerozyma, Candida, Fusarium, Cerrena and Pseudomonas. The sequences were submitted to NCBI GenBank. Crude extracellular phosphatase from cell-free culture supernatant were reacted in p-nitrophenolphosphate. Subsequently, their alkaline phosphatase activities were compared. All tested strains produced phosphatase at different pH, temperature, incubation time and substrate concentration which were used as biomarkers for microbial metabolic activity. The order of optimal phosphatase production was observed as: Cerrena sp > Aspergillus sp >M. guilliermondii > A. aculeatus > F. proliferatum > P. aeruginosa > C. tropicalis > M. caribbica. Morphological studies and microbial enzymatic activity confirm the hypothesis that heavy pigmentation and phosphatase production are major indices of discoloration on biodeteriorating painted walls in a typical tropical environment like Nigeria. Kruskal-Wallis non-parametric test revealed that there was no statistically significant difference in phosphatase production at the different environmental conditions examined except at different time intervals.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.