Production of Extremely Alkaliphilic, Halotolerent, Detergent, and Thermostable Mannanase by the Free and Immobilized Cells of Bacillus halodurans PPKS-2. Purification and Characterization
The alkaliphilic Bacillus halodurans strain PPKS-2 was shown to produce extracellular extreme alkaliphilic, halotolerent, detergent, and thermostable mannanase activity. The cultural conditions for the maximum enzyme production were optimized with respect to pH, temperature, NaCl, and inexpensive ag...
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creator | Vijayalaxmi, S. Prakash, P. Jayalakshmi, S. K. Mulimani, V. H. Sreeramulu, K. |
description | The alkaliphilic
Bacillus halodurans
strain PPKS-2 was shown to produce extracellular extreme alkaliphilic, halotolerent, detergent, and thermostable mannanase activity. The cultural conditions for the maximum enzyme production were optimized with respect to pH, temperature, NaCl, and inexpensive agro wastes as substrates. Mannanase production was enhanced more than 4-fold in the presence of 1 % defatted copra meal and 0.5 % peptone or feather hydrolysate at pH 11 and 40 °C. Mannanase was purified to 10.3-fold with 34.6 % yield by ion exchange and gel filtration chromatography methods. Its molecular mass was estimated to be 22 kDa by SDS-PAGE. The mannanase had maximal activity at pH 11 and 70 °C. This enzyme was active over a broad range of NaCl (0–16 %) and thermostable retaining 100 % of the original activity at 70 °C for 3 h. Immobilization of whole cells proved to be effective for continuous production of mannanase. Since the strain PPKS-2 grows on cheaper agro wastes such as defatted copra meal, corn husk, jowar bagasse, and wheat bran, these can be exploited for mannanase production on an industrial scale. |
doi_str_mv | 10.1007/s12010-013-0333-9 |
format | Article |
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Bacillus halodurans
strain PPKS-2 was shown to produce extracellular extreme alkaliphilic, halotolerent, detergent, and thermostable mannanase activity. The cultural conditions for the maximum enzyme production were optimized with respect to pH, temperature, NaCl, and inexpensive agro wastes as substrates. Mannanase production was enhanced more than 4-fold in the presence of 1 % defatted copra meal and 0.5 % peptone or feather hydrolysate at pH 11 and 40 °C. Mannanase was purified to 10.3-fold with 34.6 % yield by ion exchange and gel filtration chromatography methods. Its molecular mass was estimated to be 22 kDa by SDS-PAGE. The mannanase had maximal activity at pH 11 and 70 °C. This enzyme was active over a broad range of NaCl (0–16 %) and thermostable retaining 100 % of the original activity at 70 °C for 3 h. Immobilization of whole cells proved to be effective for continuous production of mannanase. Since the strain PPKS-2 grows on cheaper agro wastes such as defatted copra meal, corn husk, jowar bagasse, and wheat bran, these can be exploited for mannanase production on an industrial scale.</description><identifier>ISSN: 0273-2289</identifier><identifier>EISSN: 1559-0291</identifier><identifier>DOI: 10.1007/s12010-013-0333-9</identifier><identifier>PMID: 23839508</identifier><identifier>CODEN: ABIBDL</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Agricultural wastes ; Bacillus - cytology ; Bacillus - growth & development ; Bacillus - metabolism ; Bacillus halodurans ; Bacteria ; Bagasse ; Batch Cell Culture Techniques ; beta-Mannosidase - antagonists & inhibitors ; beta-Mannosidase - biosynthesis ; beta-Mannosidase - isolation & purification ; beta-Mannosidase - metabolism ; Biochemistry ; Biological and medical sciences ; Biotechnology ; Carbon - metabolism ; Cells, Immobilized - metabolism ; Chemistry ; Chemistry and Materials Science ; Detergents ; Detergents - pharmacology ; Dose-Response Relationship, Drug ; Enzyme Inhibitors - pharmacology ; Enzyme Stability ; Enzymes ; Fermentation ; Fundamental and applied biological sciences. Psychology ; General aspects ; Hydrogen-Ion Concentration ; Immobilization techniques ; Kinetics ; Methods. Procedures. Technologies ; Nitrogen - metabolism ; Peptones ; Sodium chloride ; Sodium Chloride - pharmacology ; Temperature ; Triticum aestivum ; Wheat bran</subject><ispartof>Applied biochemistry and biotechnology, 2013-09, Vol.171 (2), p.382-395</ispartof><rights>Springer Science+Business Media New York 2013</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-cf1797794fd4bee9a8047d3768bb09f622bb1312d3b1fb3324c4449293dc5d5f3</citedby><cites>FETCH-LOGICAL-c435t-cf1797794fd4bee9a8047d3768bb09f622bb1312d3b1fb3324c4449293dc5d5f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12010-013-0333-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12010-013-0333-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27774039$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23839508$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vijayalaxmi, S.</creatorcontrib><creatorcontrib>Prakash, P.</creatorcontrib><creatorcontrib>Jayalakshmi, S. K.</creatorcontrib><creatorcontrib>Mulimani, V. H.</creatorcontrib><creatorcontrib>Sreeramulu, K.</creatorcontrib><title>Production of Extremely Alkaliphilic, Halotolerent, Detergent, and Thermostable Mannanase by the Free and Immobilized Cells of Bacillus halodurans PPKS-2. Purification and Characterization</title><title>Applied biochemistry and biotechnology</title><addtitle>Appl Biochem Biotechnol</addtitle><addtitle>Appl Biochem Biotechnol</addtitle><description>The alkaliphilic
Bacillus halodurans
strain PPKS-2 was shown to produce extracellular extreme alkaliphilic, halotolerent, detergent, and thermostable mannanase activity. The cultural conditions for the maximum enzyme production were optimized with respect to pH, temperature, NaCl, and inexpensive agro wastes as substrates. Mannanase production was enhanced more than 4-fold in the presence of 1 % defatted copra meal and 0.5 % peptone or feather hydrolysate at pH 11 and 40 °C. Mannanase was purified to 10.3-fold with 34.6 % yield by ion exchange and gel filtration chromatography methods. Its molecular mass was estimated to be 22 kDa by SDS-PAGE. The mannanase had maximal activity at pH 11 and 70 °C. This enzyme was active over a broad range of NaCl (0–16 %) and thermostable retaining 100 % of the original activity at 70 °C for 3 h. Immobilization of whole cells proved to be effective for continuous production of mannanase. Since the strain PPKS-2 grows on cheaper agro wastes such as defatted copra meal, corn husk, jowar bagasse, and wheat bran, these can be exploited for mannanase production on an industrial scale.</description><subject>Agricultural wastes</subject><subject>Bacillus - cytology</subject><subject>Bacillus - growth & development</subject><subject>Bacillus - metabolism</subject><subject>Bacillus halodurans</subject><subject>Bacteria</subject><subject>Bagasse</subject><subject>Batch Cell Culture Techniques</subject><subject>beta-Mannosidase - antagonists & inhibitors</subject><subject>beta-Mannosidase - biosynthesis</subject><subject>beta-Mannosidase - isolation & purification</subject><subject>beta-Mannosidase - metabolism</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Carbon - metabolism</subject><subject>Cells, Immobilized - metabolism</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Detergents</subject><subject>Detergents - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Enzyme Stability</subject><subject>Enzymes</subject><subject>Fermentation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Hydrogen-Ion Concentration</subject><subject>Immobilization techniques</subject><subject>Kinetics</subject><subject>Methods. Procedures. Technologies</subject><subject>Nitrogen - metabolism</subject><subject>Peptones</subject><subject>Sodium chloride</subject><subject>Sodium Chloride - pharmacology</subject><subject>Temperature</subject><subject>Triticum aestivum</subject><subject>Wheat bran</subject><issn>0273-2289</issn><issn>1559-0291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNks1u1DAUhSMEokPhAdggSwiJRVP8l3G8LNOWVhQxEmUd2c51x8WJp3YidfpsPBzOzPAjJCRWtuzP59x7fYriJcHHBGPxLhGKCS4xYSVmjJXyUTEjVSVLTCV5XMwwFayktJYHxbOUbjEmtK7E0-KAsprJCtez4vsyhnY0gws9Chad3Q8ROvAbdOK_Ke_WK-edOUIXyocheIjQD0foFAaIN9ut6lt0vYLYhTQo7QF9Un2vepUA6Q0aVoDOI8AWu-y6oLPcA7RoAd6nyfC9Ms77MaFVdmjHqPqElsuPX0p6jJZjdNYZtS1uUlisVFQme7uH7eHz4olVPsGL_XpYfD0_u15clFefP1wuTq5Kw1k1lMYSIYWQ3LZcA0hVYy5aJua11ljaOaVaE0ZoyzSxmjHKDedcUslaU7WVZYfF253uOoa7EdLQdC6Z3ILqIYypIZwzJmhd0_9As5HM4ycZff0XehvG2OdGJorhea5QZIrsKBNDShFss46uU3HTENxMKWh2KWhyCpopBY3Mb17tlUfdQfvrxc9vz8CbPaCSUd7msRuXfnNCCI7ZJER3XMpX_Q3EP0r8p_sPJVHK8w</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Vijayalaxmi, S.</creator><creator>Prakash, P.</creator><creator>Jayalakshmi, S. K.</creator><creator>Mulimani, V. H.</creator><creator>Sreeramulu, K.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>20130901</creationdate><title>Production of Extremely Alkaliphilic, Halotolerent, Detergent, and Thermostable Mannanase by the Free and Immobilized Cells of Bacillus halodurans PPKS-2. Purification and Characterization</title><author>Vijayalaxmi, S. ; Prakash, P. ; Jayalakshmi, S. K. ; Mulimani, V. H. ; Sreeramulu, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-cf1797794fd4bee9a8047d3768bb09f622bb1312d3b1fb3324c4449293dc5d5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Agricultural wastes</topic><topic>Bacillus - cytology</topic><topic>Bacillus - growth & development</topic><topic>Bacillus - metabolism</topic><topic>Bacillus halodurans</topic><topic>Bacteria</topic><topic>Bagasse</topic><topic>Batch Cell Culture Techniques</topic><topic>beta-Mannosidase - antagonists & inhibitors</topic><topic>beta-Mannosidase - biosynthesis</topic><topic>beta-Mannosidase - isolation & purification</topic><topic>beta-Mannosidase - metabolism</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Carbon - metabolism</topic><topic>Cells, Immobilized - metabolism</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Detergents</topic><topic>Detergents - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Enzyme Stability</topic><topic>Enzymes</topic><topic>Fermentation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Hydrogen-Ion Concentration</topic><topic>Immobilization techniques</topic><topic>Kinetics</topic><topic>Methods. Procedures. Technologies</topic><topic>Nitrogen - metabolism</topic><topic>Peptones</topic><topic>Sodium chloride</topic><topic>Sodium Chloride - pharmacology</topic><topic>Temperature</topic><topic>Triticum aestivum</topic><topic>Wheat bran</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vijayalaxmi, S.</creatorcontrib><creatorcontrib>Prakash, P.</creatorcontrib><creatorcontrib>Jayalakshmi, S. K.</creatorcontrib><creatorcontrib>Mulimani, V. 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K.</au><au>Mulimani, V. H.</au><au>Sreeramulu, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of Extremely Alkaliphilic, Halotolerent, Detergent, and Thermostable Mannanase by the Free and Immobilized Cells of Bacillus halodurans PPKS-2. Purification and Characterization</atitle><jtitle>Applied biochemistry and biotechnology</jtitle><stitle>Appl Biochem Biotechnol</stitle><addtitle>Appl Biochem Biotechnol</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>171</volume><issue>2</issue><spage>382</spage><epage>395</epage><pages>382-395</pages><issn>0273-2289</issn><eissn>1559-0291</eissn><coden>ABIBDL</coden><abstract>The alkaliphilic
Bacillus halodurans
strain PPKS-2 was shown to produce extracellular extreme alkaliphilic, halotolerent, detergent, and thermostable mannanase activity. The cultural conditions for the maximum enzyme production were optimized with respect to pH, temperature, NaCl, and inexpensive agro wastes as substrates. Mannanase production was enhanced more than 4-fold in the presence of 1 % defatted copra meal and 0.5 % peptone or feather hydrolysate at pH 11 and 40 °C. Mannanase was purified to 10.3-fold with 34.6 % yield by ion exchange and gel filtration chromatography methods. Its molecular mass was estimated to be 22 kDa by SDS-PAGE. The mannanase had maximal activity at pH 11 and 70 °C. This enzyme was active over a broad range of NaCl (0–16 %) and thermostable retaining 100 % of the original activity at 70 °C for 3 h. Immobilization of whole cells proved to be effective for continuous production of mannanase. Since the strain PPKS-2 grows on cheaper agro wastes such as defatted copra meal, corn husk, jowar bagasse, and wheat bran, these can be exploited for mannanase production on an industrial scale.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>23839508</pmid><doi>10.1007/s12010-013-0333-9</doi><tpages>14</tpages></addata></record> |
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subjects | Agricultural wastes Bacillus - cytology Bacillus - growth & development Bacillus - metabolism Bacillus halodurans Bacteria Bagasse Batch Cell Culture Techniques beta-Mannosidase - antagonists & inhibitors beta-Mannosidase - biosynthesis beta-Mannosidase - isolation & purification beta-Mannosidase - metabolism Biochemistry Biological and medical sciences Biotechnology Carbon - metabolism Cells, Immobilized - metabolism Chemistry Chemistry and Materials Science Detergents Detergents - pharmacology Dose-Response Relationship, Drug Enzyme Inhibitors - pharmacology Enzyme Stability Enzymes Fermentation Fundamental and applied biological sciences. Psychology General aspects Hydrogen-Ion Concentration Immobilization techniques Kinetics Methods. Procedures. Technologies Nitrogen - metabolism Peptones Sodium chloride Sodium Chloride - pharmacology Temperature Triticum aestivum Wheat bran |
title | Production of Extremely Alkaliphilic, Halotolerent, Detergent, and Thermostable Mannanase by the Free and Immobilized Cells of Bacillus halodurans PPKS-2. Purification and Characterization |
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