Isolation and identification of protease‐producing bacteria from sludge and sediment soil around Adama, Ethiopia

https://doi.org/10.22146/ijbiotech.63987

Yeshaneh Adimasu Lemenh(1*), Teshome Geremew Biru(2), Adinew Zewdu Chernet(3), Feleke Belachew Lema(4)

(1) Department of Applied Biology, School of Applied Natural Science, Adama Science and Technology University (ASTU), Adama, Ethiopia
(2) Department of Applied Biology, School of Applied Natural Science, Adama Science and Technology University (ASTU), Adama, Ethiopia
(3) Oromia Public Health Research Capacity Building and Quality Assurance Laboratory (OPHRCBQAL), Adama, Ethiopia
(4) Oromia Public Health Research Capacity Building and Quality Assurance Laboratory (OPHRCBQAL), Adama, Ethiopia
(*) Corresponding Author

Abstract


Proteases are enzymes used in industries such the production and processing of detergents, food, leather, and silk. The aim of this study was to isolate and identify protease‐producing bacteria from a sludge disposal site and from sediments. Soil samples were collected separately from the selected area. Samples weighing 1 g were serially diluted and spread onto skim milk agar. A total of 16 bacteria species were isolated from the study samples. Four bacterial isolates showed high proteolytic activity and were selected for enzymatic study based on their zone of proteolysis. The isolates were identified based on biochemical tests. The results indicated that the isolated bacteria were E. coli (99.69%), Pseudomonas putrefaciens (Shewanella putrefaciens) (91.61%), Bacillus carboniphilus (92.78%), and Lysinibacillus sphaericus (98.4%). The crude protease enzymes produced by these bacterial isolates showed promising results for application in dehairing and destaining as detergent additives. Bacillus carboniphilus showed the best level of activity and was selected as the most potent protease‐producing bacteria for both dehairing and destaining ability. Soils from sludge disposal sites and sediments from around tannery wastes could be good sources from which to isolate alkaline protease‐producing bacteria.


Keywords


Alkaline protease; dehairing; destaining; hydrolysis; sediment

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References

Aftab S, Ahmed S, Saeed S, Rasool SA. 2006. Screening, isolation and characterization of alkaline protease producing bacteria from soil. Pak J Biol Sci. 9(11):2122–2126. doi:10.3923/pjbs.2006.2122.2126.

Bayoumi RA, Atta HM, El­Sehrawy MH. 2012. Bioremediation of khormah slaughter house wastes by production of thermoalkalistable lipase for application in leather industries. Life Sci J. 9(4):1324–1335.

Dudhgara PR, Sunil B, Anjana G. 2015. Hide dehairing and laundry detergent compatibility testing of thermostable and solvents tolerant alkaline protease from hot spring isolate bacillus cohniiU3. OnLine J Biol Sci. 15(3):152–161. doi:10.3844/ojbsci.2015.152.161.

Fu Z, Hamid SBA, Razak CNA, Basri M, Bakar Salleh A, Rahman RNZA. 2003. Secretory expression in Escherichia coli and single­step purification of a heat­stable alkaline protease. Protein Expression and Purification 28(1):63–68. doi:10.1016/S1046­ 5928(02)00637­X.

Gessesse A, Mulaa F, Lyantagaye S, L NW, Mattiasson B, Pandey A. 2011. Industrial enzymes for sustainable bio­economy: Large scale production and application in industry, environment, and agriculture in eastern africa.

Gupta R, Beg Q, Lorenz P. 2002. Bacterial alkaline proteases: Molecular approaches and industrial applications. Appl Microbiol Biotechnol. 59(1):15–32. doi:10.1007/s00253­002­0975­y.

Kocher GS, Mishra S. 2010. Immobilization of Bacillus circulans MTCC 7906 for enhanced production of alkaline protease under batch and packed bed fermentation conditions. Internet J Microbiol. 7(2). doi:10.5580/2599.

Mohammed I, Hampton SE, Ashall L, Hildebrandt ER, Kutlik RA, Manandhar SP, Floyd BJ, Smith HE, Dozier JK, Distefano MD, Schmidt WK, Dore TM. 2016. 8­Hydroxyquinoline­based inhibitors of the Rce1 protease disrupt Ras membrane localization in human cells. Bioorg Med Chem. 24(2):160–178. doi:10.1016/j.bmc.2015.11.043.

Murray CW, Callaghan O, Chessari G, Cleasby A, Congreve M, Frederickson M, Hartshorn MJ, McMenamin R, Patel S, Wallis N. 2007. Application of fragment screening by X­ray crystallography to β­secretase. J Med Chem. 50(6):1116–1123. doi:10.1021/jm0611962.

Nikolic M, Terzic­Vidojevic A, Jovcic B, Begovic J, Golic N, Topisirovic L. 2008. Characterization of lactic acid bacteria isolated from Bukuljac, a homemade goat’s milk cheese. Int J Food Microbiol. 122(1­2):162–170. doi:10.1016/j.ijfoodmicro.2007.11.075.

Sneath PH. 1986. Endospore­forming gram­positive rods and cocci., booktitle = Bergey’s manual of systematic bacteriology. p. 1104–1207.

Tallur PN, Sajjan DB, Mulla SI, Talwar MP, Pragasam A, Nayak VM, Ninnekar HZ, Bhat SS. 2016. Characterization of antibiotic resistant and enzyme producing bacterial strains isolated from the Arabian Sea. 3 Biotech. 6(1):1–11. doi:10.1007/s13205­015­0332­3.

Wirth MC, Berry C, Walton WE, Federici BA. 2014. Mtx toxins from Lysinibacillus sphaericus enhance mosquitocidal cry­toxin activity and suppress cryresistance in Culex quinquefasciatus. J Invertebr Pathol. 115(1):62–67. doi:10.1016/j.jip.2013.10.003.



DOI: https://doi.org/10.22146/ijbiotech.63987

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