PURIFICATION AND MOLECULAR WEIGHT DETERMINATION OF KERATINASE ISOLATED FROM STREPTOMYCES MALAYSIENSIS

Authors

  • M. Pavani Srinivasarao College of pharmacy, Visakhapatnam
  • G. Girijasankar Professor, Andhra University, Visakhapatnam
  • K. Mallika Andhra University, Visakhapatnam
  • G. Vidhya Sagar Srinivasarao college of pharmacy, Visakhapatnam

DOI:

https://doi.org/10.22159/ijpps.2017v9i11.21442

Keywords:

Streptomyces, Keratinase, Purification, Feather powder, Environment protection

Abstract

Objective: The aim of the present study was to purify and determine the molecular weight of keratinase isolated from Streptomyces malaysiensis.

Methods: For that purpose purification was done using ammonium sulphate and Sephadex-LH 100 column chromatography. Further, the fractions were pooled and subjected to molecular weight determination using sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

Results: The obtained results showed keratinase with 47.57% recovery, 3.5-fold purification and an estimated molecular mass of 27,000 Da. Keratinase showed an optimal activity at 60 οC and pH 8. Keratinase activity of the purified product was assayed with feather powder as a substrate. The isolated strain was identified as Streptomyces malaysiensis based on phylogenetic tree analysis. The strain isolated from termite mound soil showed the highest keratinase activity, which could be considered a microorganism of environmental origin.

Conclusion: The production of keratinase on simple media with feathers as sole source allowing its production from the cheap substrate and a commercial production with low production cost. Stability in the presence of detergents, surfactants and solvents make this keratinase extremely useful for a biotechnological process involving keratin.

Downloads

Download data is not yet available.

References

Voet D, Voet JG. Three dimensional structures of proteins. In: Stiefel J. ed Biochemistry. 2nd edition. Wiley: NewYork; 1995. p. 154-6.

Schrooyen PMM, Dijkstra PJ, Oberthur RC, Bantjes A, Feijen J. Partially carboxymethylated feather keratins 2. Thermal and mechanical properties of films. J Agric Food Chem 2001;49:221-30.

Papadopoulos MC. The effect of enzymatic treatment on amino acid content and nitrogen characteristics of feather meal. Anim Feed Sci Technol 1986;16:151-6.

Ignatova Z, Gousterova A, Spassov G, Nedkov P. Isolation and partial characterization of extracellular keratinase from wool degrading thermophilic actinomycetes strain Thermoactinomyces candidus. Can J Microbiol 1999;45:217-22.

Ramnani P, Singh R, Gupta R. Keratinolytic potential of Bacillus licheniformis RG1: structural and biochemical mechanism of feather degradation. Can J Microbiol 2005;51:191-6.

Sohnle PG, Wagner DK. Fungal infections, cutaneous. In: J Lederberg. ed. Encyclopedia of microbiology. 2nd edition. San Diego Academic; 2000. p. 451-9.

Onifade AA, A1-Sane NA, AI-Musallam AA, Al-Zarban S. A review: potentials for biotechnological applications of keratin degrading microorganisms and their enzymes for nutritional improvement of feathers and other keratins as livestock free resources. Bioresour Technol 1998;66:1-11.

Lin X, Inglis GD, Yanke LJ, Cheng KJ. Selection and characterization of the feather-degrading bacterium from conola meal compost. J Ind Microbiol Biotechnol 1999;23:149-53.

Riffel A, Lucas F, Heeb P, Brandelli A. Characterization of a new keratinolytic bacterium that completely degrades native feather keratin. Arch Microbiol 2003;179:258-65.

Friedrich AB, Antranikian G. Keratin degradation by Fervidobacterium pennavorans, a novel thermophilic anaerobic species of the order thermotogales. Appl Environ Microbiol 1996;62:2875-82.

De Toni CH, Richter MF, Chagas JR, Henriques JAP, Termignoni C. Purification and characterization of an alkaline serine endopeptidase from a feather-degrading Xanthomonas maltophila strain. Can J Microbiol 2002;48:342-8.

Ellaiah P, Ramana T, Bapi Raju KVVSN, Sujatha P, Uma sankar A. Investigations on marine actinomycetes from the Bay of Bengal near kakinada coast of Andhra Pradesh. Asian J Microbiol Biotechnol Environ Sci 2004;6:53–6.

Zerdani I, Faid M, Malik A. Feather wastes digestion by newly isolated strain Bacillus sp. In Morocco. Afr J Biotechnol 2004;3:67-70.

Bockle B, Galunski B, Muller R. Characterization of a keratinolytic serine protease from Streptomyces pactum DSM40530. Appl Environ Microbiol 1995;61:3705-10.

Dozie INS, Okeke CN, Unaeze NC. A thermostable, alkaline-active, keratinolytic proteinase from Chrysosporium keratinophilum. World J Microbiol Biotechnol 1994;10:563-7.

Jayalakshmi T, Krishnamoorthy P, Ramesh kumar G, Sivamani P. Purification and characterization of the keratinase enzyme from Streptomyces species JRS 19. New York Sci J 2011;4:59-67.

Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970;227:680-5.

Saitou N, Nei M. The neighbour-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987;4:406-25.

Kimura M. A sample method for estimating the evolutionary rate of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 1980;16:111-20.

Smriti S, Anju Rawat S, Abhinav G, Anil Kumar S, Gopalan N, Hotam Singh C. Keratinloytic actinomycetes isolated from poultry Waste. J Chem Pharm Res 2012;4:4107-11.

Kuster E, Williams S. Selection of media for isolation of Streptomycetes. Nature 1964;202:928-9.

Ellaiah P, Ramana T, Bapi Raju KVVSN, Sujatha P, Uma sankar A. Investigations on marine actinomycetes from the bay of Bengal near kakinada coast of Andhra Pradesh. Asian J Microbiol Biotechnol Environ Sci 2004;6:53-6.

Sujatha P, Swethalatha P. Isolation and screening of novel Streptomyces from sediments of the bay of bengal near srikakulam coast. Int J Curr Pharm Res 2017;9:40-4.

Noval JJ, Nickerson WJ. Decomposition of native keratin by Streptomyces fradiae. J Bacteriol 1959;77:251-63.

Prakash P, Jayalakshmi SK, Sreeramulu K. Production of keratinase by free and immobilized cells of Bacillus halodurans strain PPKS-2: partial characterization and its application in feather degradation and dehairing of the goatskin. Appl Biochem Biotechnol 2010;160:1909-20.

Riffel A, Brandelli A, Bellato CM, Souza GHMF, Eberlin MN, Tavares FCA. Purification and characterization of a keratinolytic metalloprotease from Chryseobacterium sp. kr6. J Biotechnol 2007;128:693-703.

Singh C, Parmar RS, Jadon P, Kumar A. Characterization of actinomycetes against phytopathogenic fungi of glycine max (L.). Asian J Pharm Clin Res 2016;9 Suppl 1:216-9.

Savitha G Joshi, Tejashwini MM, Revati N, Sridevi R, Roma D. Isolation, identification and characterization of a feather-degrading bacterium. Int J Poult Sci 2007;6:689-93.

Published

01-11-2017

How to Cite

Pavani, M., G. Girijasankar, K. Mallika, and G. V. Sagar. “PURIFICATION AND MOLECULAR WEIGHT DETERMINATION OF KERATINASE ISOLATED FROM STREPTOMYCES MALAYSIENSIS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 9, no. 10, Nov. 2017, pp. 154-8, doi:10.22159/ijpps.2017v9i11.21442.

Issue

Section

Original Article(s)