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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Iraninan Biology Society</PublisherName>
				<JournalTitle>Journal of Cellular and Molecular Research
(Iranian Journal of Biology)</JournalTitle>
				<Issn>2383-2738</Issn>
				<Volume>38</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>06</Month>
					<Day>22</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Optimization of Bacillus sp. AGh1‎‏ ‏culture medium for‏ ‏production of Endo-1,4-β-D-glucanase and the enzyme characterization</ArticleTitle>
<VernacularTitle>Optimization of Bacillus sp. AGh1‎‏ ‏culture medium for‏ ‏production of Endo-1,4-β-D-glucanase and the enzyme characterization</VernacularTitle>
			<FirstPage>127</FirstPage>
			<LastPage>142</LastPage>
			<ELocationID EIdType="pii">2295</ELocationID>
			
<ELocationID EIdType="doi">10.22034/cmr.2025.2295</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Hasan</FirstName>
					<LastName>Diba</LastName>
<Affiliation>Biotechnology Department, Iranian Research Organization for Science and Technology &amp;lrm;&amp;lrm;(IROST), Tehran, Iran, &amp;lrm;</Affiliation>

</Author>
<Author>
					<FirstName>Jafar</FirstName>
					<LastName>Hemmat</LastName>
<Affiliation>Biotechnology Department, Iranian Research Organization for Science and Technology &amp;lrm;&amp;lrm;(IROST), Tehran, Iran, &amp;lrm;</Affiliation>

</Author>
<Author>
					<FirstName>Mohsen</FirstName>
					<LastName>Vaez</LastName>
<Affiliation>Biotechnology Department, Iranian Research Organization for Science and Technology &amp;lrm;&amp;lrm;(IROST), Tehran, Iran, &amp;lrm;</Affiliation>

</Author>
<Author>
					<FirstName>Arun</FirstName>
					<LastName>Goyal</LastName>
<Affiliation>Department of Biotechnology, Indian Institute of Technology Guwahati (IITG), Assam, India.</Affiliation>
<Identifier Source="ORCID">0000-0002-2741-9122</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>07</Month>
					<Day>26</Day>
				</PubDate>
			</History>
		<Abstract>Thermostable Endo-1,4-β-D-glucanase, known as a density reducer in cellulose ‎degradation, is one of the most widely used enzymes in industries. In this study, the ‎thermostability of Endo-1, 4-β-D-glucanase produced by Bacillus sp. AGh1 which was isolated from ‎a hot-spring in Ardabil province, Iran was evaluated. The enzyme production was optimized through two steps. Rice bran and yeast extract ‎were determination as the effective factors for enzyme production by Plackett-‎Burman method, and optimization of culture medium was performed by Response Surface ‎Methodology method. The amount of mentioned effective factors for producing the enzyme ‎were 58.8 and 14.87 g L-1, respectively. The optimum temperature and pH ‎for the enzyme activity were 70 ̊C and pH 5.6, respectively. Accordingly, Bacillus sp. ‎AGh1 can produce endo-1,4-β-D-glucanase enzyme from rice bran as cheap raw ‎material with suitable activity. Consequently, the enzyme has functional at the wide ‎range of pH and may be applied which needs more studies.‎</Abstract>
			<OtherAbstract Language="FA">Thermostable Endo-1,4-β-D-glucanase, known as a density reducer in cellulose ‎degradation, is one of the most widely used enzymes in industries. In this study, the ‎thermostability of Endo-1, 4-β-D-glucanase produced by Bacillus sp. AGh1 which was isolated from ‎a hot-spring in Ardabil province, Iran was evaluated. The enzyme production was optimized through two steps. Rice bran and yeast extract ‎were determination as the effective factors for enzyme production by Plackett-‎Burman method, and optimization of culture medium was performed by Response Surface ‎Methodology method. The amount of mentioned effective factors for producing the enzyme ‎were 58.8 and 14.87 g L-1, respectively. The optimum temperature and pH ‎for the enzyme activity were 70 ̊C and pH 5.6, respectively. Accordingly, Bacillus sp. ‎AGh1 can produce endo-1,4-β-D-glucanase enzyme from rice bran as cheap raw ‎material with suitable activity. Consequently, the enzyme has functional at the wide ‎range of pH and may be applied which needs more studies.‎</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Bacillus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">cellulase</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Thermostability</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Endo-1</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">4-&amp;‌‌‌‌‌‌‌‌beta</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">-D-glucanase</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://cell.ijbio.ir/article_2295_16026d60ff9b54410b3435b403afd226.pdf</ArchiveCopySource>
</Article>
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