Alkaline Protease Production From Alkalophilic Bacillus Sp. Isolated From Natural Habitats

dc.contributor.author Gençkal, Hande
dc.contributor.author Tarı, Canan
dc.coverage.doi 10.1016/j.enzmictec.2005.12.004
dc.date.accessioned 2016-10-10T12:52:09Z
dc.date.available 2016-10-10T12:52:09Z
dc.date.issued 2006
dc.description.abstract Bacillus strains isolated under extreme alkaline conditions (Izmir, Turkey), were screened and identified for high alkaline protease activity. Strains with high protease yields were optimized with respect to inoculum concentration, temperature, agitation speed, initial medium pH and incubation time. Three Bacillus strains coded as I18, L18 and L21 showed high potential, for alkaline protease activity (160-222 U/ml) among 85 isolates. The specific growth rates were estimated from the growth curves as 0.49 h-1 for I18, as 0.6 and 0.7 h-1 for L18 and L21, respectively. The optimum temperatures were determined as 30 °C for strain I18 and 37 °C for the strains L18 and L21. Similarly, the optimum agitation speeds were 100 rpm for I18 and 180 rpm for L18 and L21. For all three strains, the optimum inoculation ratio and incubation time, were determined as 5% (v/v) and 96 h, respectively. The optimum initial media pH was found as pH 10 for strain L18 and L21. Bacillus sp. L21 with the highest specific protease activity (60 U/mg protein) and a broader pH range was chosen for further study. The biomass and product yield for this strain was determined as 0.023 g cell/g glucose and 0.021 U/g glucose, respectively. The crude enzyme of this strain was further characterized and was determined as a bleach stable, serine alkaline protease with an optimum temperature of 60 °C and a pH of 11, with a potential to be a candidate for the applications in the detergent industry. en_US
dc.description.sponsorship İzmir Institute of Technology en_US
dc.identifier.citation Gençkal, H., and Tarı, C. (2006). Alkaline protease production from alkalophilic Bacillus sp. isolated from natural habitats. Enzyme and Microbial Technology, 39(4), 703-710. doi:10.1016/j.enzmictec.2005.12.004 en_US
dc.identifier.doi 10.1016/j.enzmictec.2005.12.004 en_US
dc.identifier.doi 10.1016/j.enzmictec.2005.12.004
dc.identifier.issn 0141-0229
dc.identifier.scopus 2-s2.0-33745213791
dc.identifier.uri http://doi.org/10.1016/j.enzmictec.2005.12.004
dc.identifier.uri https://hdl.handle.net/11147/2199
dc.language.iso en en_US
dc.publisher Elsevier Ltd. en_US
dc.relation.ispartof Enzyme and Microbial Technology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Enzyme kinetics en_US
dc.subject Alkaline protease en_US
dc.subject Bacillus sp. en_US
dc.subject Enzyme production en_US
dc.subject Microbial enzymes en_US
dc.title Alkaline Protease Production From Alkalophilic Bacillus Sp. Isolated From Natural Habitats en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Gençkal, Hande
gdc.author.institutional Tarı, Canan
gdc.author.yokid 41331
gdc.bip.impulseclass C4
gdc.bip.influenceclass C4
gdc.bip.popularityclass C4
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Food Engineering en_US
gdc.description.endpage 710 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 703 en_US
gdc.description.volume 39 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W2058584290
gdc.identifier.wos WOS:000238932500028
gdc.index.type WoS
gdc.index.type Scopus
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.impulse 10.0
gdc.oaire.influence 9.523459E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Enzyme kinetics
gdc.oaire.keywords Bacillus sp.
gdc.oaire.keywords Alkaline protease
gdc.oaire.keywords Microbial enzymes
gdc.oaire.keywords Enzyme production
gdc.oaire.popularity 2.3574001E-8
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0106 biological sciences
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 03 medical and health sciences
gdc.oaire.sciencefields 01 natural sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 5.94450001
gdc.openalex.normalizedpercentile 0.96
gdc.openalex.toppercent TOP 10%
gdc.opencitations.count 83
gdc.plumx.crossrefcites 65
gdc.plumx.mendeley 103
gdc.plumx.scopuscites 120
gdc.scopus.citedcount 120
gdc.wos.citedcount 110
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