Enhanced degradation of caffeine by immobilized cells of Pseudomonas sp. in agar–agar matrix using statistical approach
Previously, we isolated caffeine degrading Pseudomonas strain from soil of coffee plantation area, which could utilize caffeine as sole carbon and nitrogen source and could tolerate caffeine up to 20 g/L. In this study, caffeine degradation by immobilized cells of this strain was investigated. Vario...
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Veröffentlicht in: | Biochemical engineering journal 2009-05, Vol.44 (2), p.136-141 |
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creator | Gummadi, Sathyanarayana N. Ganesh, K.B. Santhosh, Devarai |
description | Previously, we isolated caffeine degrading
Pseudomonas strain from soil of coffee plantation area, which could utilize caffeine as sole carbon and nitrogen source and could tolerate caffeine up to 20
g/L. In this study, caffeine degradation by immobilized cells of this strain was investigated. Various matrices were considered and agar–agar was chosen based on degradation rate (0.08
g/(L
h)), bead stability and reusability. Further, immobilization parameters, viz., bead size (mm), agar–agar concentration % (w/v) and cell concentration (g/L) were optimized using central composite design. The optimal conditions of cell concentration, agar–agar concentration and bead size were 7.8
g/L, 5% (w/v) and 6.2
mm. Under optimal conditions, caffeine degradation rate was found to 0.15
g/(L
h), which closely agrees with the model predicted values. This is the first report on caffeine degradation at high concentrations (10
g/L) by immobilized cells of
Pseudomonas sp. Immobilization efficiency was 80%. Damköhler number is very much higher than 1, suggesting that mass transfer is the rate limiting process. |
doi_str_mv | 10.1016/j.bej.2008.11.010 |
format | Article |
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Pseudomonas strain from soil of coffee plantation area, which could utilize caffeine as sole carbon and nitrogen source and could tolerate caffeine up to 20
g/L. In this study, caffeine degradation by immobilized cells of this strain was investigated. Various matrices were considered and agar–agar was chosen based on degradation rate (0.08
g/(L
h)), bead stability and reusability. Further, immobilization parameters, viz., bead size (mm), agar–agar concentration % (w/v) and cell concentration (g/L) were optimized using central composite design. The optimal conditions of cell concentration, agar–agar concentration and bead size were 7.8
g/L, 5% (w/v) and 6.2
mm. Under optimal conditions, caffeine degradation rate was found to 0.15
g/(L
h), which closely agrees with the model predicted values. This is the first report on caffeine degradation at high concentrations (10
g/L) by immobilized cells of
Pseudomonas sp. Immobilization efficiency was 80%. Damköhler number is very much higher than 1, suggesting that mass transfer is the rate limiting process.</description><identifier>ISSN: 1369-703X</identifier><identifier>EISSN: 1873-295X</identifier><identifier>DOI: 10.1016/j.bej.2008.11.010</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Biodegradation ; Biological and medical sciences ; Biotechnology ; Diffusion reaction ; Fundamental and applied biological sciences. Psychology ; General aspects ; Immobilization ; Immobilization techniques ; Immobilized cells ; Kinetic parameters ; Methods. Procedures. Technologies ; Pseudomonas ; Submerged culture</subject><ispartof>Biochemical engineering journal, 2009-05, Vol.44 (2), p.136-141</ispartof><rights>2008 Elsevier B.V.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-29c3e34ef5258e44ffce8422878baa36a5be23e1c2a59d2cd79cc060e4886353</citedby><cites>FETCH-LOGICAL-c424t-29c3e34ef5258e44ffce8422878baa36a5be23e1c2a59d2cd79cc060e4886353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1369703X08003616$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21299313$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Gummadi, Sathyanarayana N.</creatorcontrib><creatorcontrib>Ganesh, K.B.</creatorcontrib><creatorcontrib>Santhosh, Devarai</creatorcontrib><title>Enhanced degradation of caffeine by immobilized cells of Pseudomonas sp. in agar–agar matrix using statistical approach</title><title>Biochemical engineering journal</title><description>Previously, we isolated caffeine degrading
Pseudomonas strain from soil of coffee plantation area, which could utilize caffeine as sole carbon and nitrogen source and could tolerate caffeine up to 20
g/L. In this study, caffeine degradation by immobilized cells of this strain was investigated. Various matrices were considered and agar–agar was chosen based on degradation rate (0.08
g/(L
h)), bead stability and reusability. Further, immobilization parameters, viz., bead size (mm), agar–agar concentration % (w/v) and cell concentration (g/L) were optimized using central composite design. The optimal conditions of cell concentration, agar–agar concentration and bead size were 7.8
g/L, 5% (w/v) and 6.2
mm. Under optimal conditions, caffeine degradation rate was found to 0.15
g/(L
h), which closely agrees with the model predicted values. This is the first report on caffeine degradation at high concentrations (10
g/L) by immobilized cells of
Pseudomonas sp. Immobilization efficiency was 80%. Damköhler number is very much higher than 1, suggesting that mass transfer is the rate limiting process.</description><subject>Biodegradation</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Diffusion reaction</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Immobilization</subject><subject>Immobilization techniques</subject><subject>Immobilized cells</subject><subject>Kinetic parameters</subject><subject>Methods. Procedures. Technologies</subject><subject>Pseudomonas</subject><subject>Submerged culture</subject><issn>1369-703X</issn><issn>1873-295X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kLtuGzEQRRdGDNiR_QHu2CSdNnztC6kCwY4NCHAKF-6IWe5QprC7VDirIHKVf8gf-kvMhYSUqYbFmTu8J8tuBM8FF-WXbd7iNpec17kQORf8LLsUdaWWsimeP6S3KptlxdXzRfaRaMs5L1VVXWaH2_EFRosd63AToYPJh5EFxyw4h35E1h6YH4bQ-t6_Jsxi39MM_CDcd2EIIxCjXc78yGAD8e3P33mwAabof7M9-XHDaEq5NHkLPYPdLgawL1fZuYOe8Po0F9nT3e3T6n65fvz-sPq2Xlot9ZT-bxUqja6QRY1aO2ex1lLWVd0CqBKKFqVCYSUUTSdtVzXW8pKjrutSFWqRfT7Gpqs_90iTGTzNJWDEsCcjudZKFSKB4gjaGIgiOrOLfoB4MIKb2bHZmuTYzI6NECY5TjufTuFAqZuLSaWnf4tSyKZRQiXu65HDVPSXx2jIepy1-4h2Ml3w_7nyDrj2lGM</recordid><startdate>20090515</startdate><enddate>20090515</enddate><creator>Gummadi, Sathyanarayana N.</creator><creator>Ganesh, K.B.</creator><creator>Santhosh, Devarai</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20090515</creationdate><title>Enhanced degradation of caffeine by immobilized cells of Pseudomonas sp. in agar–agar matrix using statistical approach</title><author>Gummadi, Sathyanarayana N. ; Ganesh, K.B. ; Santhosh, Devarai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-29c3e34ef5258e44ffce8422878baa36a5be23e1c2a59d2cd79cc060e4886353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Biodegradation</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Diffusion reaction</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Immobilization</topic><topic>Immobilization techniques</topic><topic>Immobilized cells</topic><topic>Kinetic parameters</topic><topic>Methods. Procedures. Technologies</topic><topic>Pseudomonas</topic><topic>Submerged culture</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gummadi, Sathyanarayana N.</creatorcontrib><creatorcontrib>Ganesh, K.B.</creatorcontrib><creatorcontrib>Santhosh, Devarai</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biochemical engineering journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gummadi, Sathyanarayana N.</au><au>Ganesh, K.B.</au><au>Santhosh, Devarai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhanced degradation of caffeine by immobilized cells of Pseudomonas sp. in agar–agar matrix using statistical approach</atitle><jtitle>Biochemical engineering journal</jtitle><date>2009-05-15</date><risdate>2009</risdate><volume>44</volume><issue>2</issue><spage>136</spage><epage>141</epage><pages>136-141</pages><issn>1369-703X</issn><eissn>1873-295X</eissn><abstract>Previously, we isolated caffeine degrading
Pseudomonas strain from soil of coffee plantation area, which could utilize caffeine as sole carbon and nitrogen source and could tolerate caffeine up to 20
g/L. In this study, caffeine degradation by immobilized cells of this strain was investigated. Various matrices were considered and agar–agar was chosen based on degradation rate (0.08
g/(L
h)), bead stability and reusability. Further, immobilization parameters, viz., bead size (mm), agar–agar concentration % (w/v) and cell concentration (g/L) were optimized using central composite design. The optimal conditions of cell concentration, agar–agar concentration and bead size were 7.8
g/L, 5% (w/v) and 6.2
mm. Under optimal conditions, caffeine degradation rate was found to 0.15
g/(L
h), which closely agrees with the model predicted values. This is the first report on caffeine degradation at high concentrations (10
g/L) by immobilized cells of
Pseudomonas sp. Immobilization efficiency was 80%. Damköhler number is very much higher than 1, suggesting that mass transfer is the rate limiting process.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.bej.2008.11.010</doi><tpages>6</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals |
subjects | Biodegradation Biological and medical sciences Biotechnology Diffusion reaction Fundamental and applied biological sciences. Psychology General aspects Immobilization Immobilization techniques Immobilized cells Kinetic parameters Methods. Procedures. Technologies Pseudomonas Submerged culture |
title | Enhanced degradation of caffeine by immobilized cells of Pseudomonas sp. in agar–agar matrix using statistical approach |
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