Production and characterization of thermostable alpha-amylase from thermophilic Anoxybacillus flavithermus sp nov SO-19

dc.contributor.author Ozdemir, Sadin
dc.contributor.author Okumus, Veysi
dc.contributor.author Ulutas, Mehmet Sefa
dc.contributor.author Dundar, Abdurrahman
dc.contributor.author Akarsubasic, Alper Tunga
dc.contributor.author Dumontet, Stefano
dc.contributor.other 21.02. Department of Medical Services and Techniques / Tıbbi Hizmetler ve Teknikleri Bölümü
dc.contributor.other 21. Vocational School of Health Services / Sağlık Hizmetleri Meslek Yüksekokulu
dc.contributor.other 01. Mardin Artuklu University / Mardin Artuklu Üniversitesi
dc.date.accessioned 14.07.201910:50:10
dc.date.accessioned 2019-07-16T20:43:59Z
dc.date.available 14.07.201910:50:10
dc.date.available 2019-07-16T20:43:59Z
dc.date.issued 2016
dc.description.abstract This study was concerned with isolation and identification of thermophilic bacteria from hot spring in Afyonkarahisar (Gecek) and optimization of a-amylase production, partial purification of alpha-amylase, and characterization of extracellular enzyme from isolated thermophilic strain 19. To characterize and identify the thermophilic isolated bacteria, morphological analysis and biochemistry tests were studied. Besides, for classification 16S rRNA gene, G-C content and DNA-DNA hybridization analysis were performed. These results indicated that strain 19 is a novel species, Anoxybacillus flavithermus sp. nov. The effects of different fermentation conditions, such as incubation time, temperature, and pH, different carbon and nitrogen sources, and surfactants on a-amylase production were investigated. Various parameters such as temperature and temperature stability, pH and pH stability, detergents and surfactants, different starches, and metal ions on influence of enzyme characterization were assayed. About 93, 87, and 81% of the activities were retained after heating the partially purified enzyme solution at 50, 60, and 70 for 240 min, respectively. Enzyme was excessively inhibited by Hg2+ (6%). The enzyme was activated by Co2+ (212%) and Mg2+ (142%). Enzyme degradated 82% of starch content in apple juice at 70 degrees C in 30 min. The molecular weight of enzyme was estimated as 96 kDa. en_US
dc.description.sponsorship Scientific Research Projects Unit of Siirt University, Turkey [BAP-2011-SIUFED-F3] en_US
dc.description.sponsorship This study was supported by Scientific Research Projects Unit of Siirt University (project code: BAP-2011-SIUFED-F3), Turkey. en_US
dc.identifier.citation Özdemir, S., Okumus, V., Ulutas, M. S., Dundar, A., Akarsubasic, A. T., & Dumontet, S. (2016). Production and characterization of thermostable α-amylase from thermophilicAnoxybacillus flavithermussp. nov. SO-19. Starch - Stärke, 68(11–12), 1244–1253. https://doi.org/10.1002/star.201500071 en_US
dc.identifier.doi 10.1002/star.201500071
dc.identifier.issn 0038-9056
dc.identifier.issn 1521-379X
dc.identifier.scopus 2-s2.0-84962670748
dc.identifier.uri https://dx.doi.org/10.1002/star.201500071
dc.identifier.uri https://hdl.handle.net/20.500.12514/1328
dc.indekslendigikaynak Web of Science en_US
dc.indekslendigikaynak Scopus en_US
dc.language.iso en en_US
dc.publisher WILEY-V C H VERLAG GMBH en_US
dc.relation.ispartof STARCH-STARKE en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Anoxybacillus flavithermus en_US
dc.subject alpha-Amylase en_US
dc.subject Apple juice industry en_US
dc.subject Detergent industry en_US
dc.subject Thermostable en_US
dc.title Production and characterization of thermostable alpha-amylase from thermophilic Anoxybacillus flavithermus sp nov SO-19 en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Dündar, Abdurrahman
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department MAÜ, Meslek Yüksekokulları, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Hizmetler ve Teknikler Bölümü en_US
gdc.description.endpage 1253 en_US
gdc.description.issue 11.Dec en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 1244 en_US
gdc.description.volume 68 en_US
gdc.description.wosquality Q2
gdc.identifier.wos WOS:000389311200025
gdc.openalex.fwci 0.285
gdc.scopus.citedcount 14
gdc.wos.citedcount 13
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