Enzymatic depilation of animal hide: Identification of elastase (LasB) from Pseudomonas aeruginosa MCM B-327 as a depilating protease

dc.contributor.author Pandeeti, Emmanuel Vijay Paul
dc.contributor.author Pitchika, Gopi Krishna
dc.contributor.author Jotshi, Jyotsna
dc.contributor.author Nilegaonkar, Smita S.
dc.contributor.author Kanekar, Pradnya P.
dc.contributor.author Siddavattam, Dayananda
dc.date.accessioned 2022-03-27T00:57:44Z
dc.date.available 2022-03-27T00:57:44Z
dc.date.issued 2011-02-25
dc.description.abstract Conventional leather processing involving depilation of animal hide by lime and sulphide treatment generates considerable amounts of chemical waste causing severe environmental pollution. Enzymatic depilation is an environmentally friendly process and has been considered to be a viable alternative to the chemical depilation process. We isolated an extracellular protease from Pseudomonas aeruginosa strain MCM B-327 with high depilation activity using buffalo hide as a substrate. This 33 kDa protease generated a peptide mass fingerprint and de novo sequence that matched perfectly with LasB (elastase), of Pseudomonas aeruginosa. In support of this data a lasB mutant of MCM B-327 strain lacked depilatory activity and failed to produce LasB. LasB heterologously over-produced and purified from Escherichia coli also exhibited high depilating activity. Moreover, reintroduction of the lasB gene to the P. aeruginosa lasB mutant via a knock-in strategy also successfully restored depilation activity thus confirming the role of LasB as the depilating enzyme. © 2011 Pandeeti et al.
dc.identifier.citation PLoS ONE. v.6(2)
dc.identifier.uri 10.1371/journal.pone.0016742
dc.identifier.uri https://dx.plos.org/10.1371/journal.pone.0016742
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/3481
dc.title Enzymatic depilation of animal hide: Identification of elastase (LasB) from Pseudomonas aeruginosa MCM B-327 as a depilating protease
dc.type Journal. Article
dspace.entity.type
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