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An ex-situ and in vitro approach towards the bioremediation of carcinogenic hexavalent chromium
Chromium, ranking the second most among toxic heavy metal pollutants in the world, causing respiratory, cardiovascular and renal problems in human beings is under study herein. We examined the biological remediation of the carcinogenic Cr (VI) polluted soils by indigenous yeast isolates. The total e...
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Published in: | Preparative biochemistry & biotechnology 2020-09, Vol.50 (8), p.842-848 |
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description | Chromium, ranking the second most among toxic heavy metal pollutants in the world, causing respiratory, cardiovascular and renal problems in human beings is under study herein. We examined the biological remediation of the carcinogenic Cr (VI) polluted soils by indigenous yeast isolates. The total element analysis of the treated sample was determined by Energy Dispersion X-ray Micro Analysis (EDXMA). The sample under study was observed to have a high concentration of 458.29 mgKg
−1
Cr (VI), determined by Atomic Absorption Spectroscopy (AAS) and DPC analysis. The most tolerant isolate designated as CSR was used for in vitro and ex-situ bioremediation studies of Cr (VI). The isolate achieved significant bioremediation of 86% in vitro and 75.12% in ex-situ method. The optimal conditions for in vitro bioremediation were found to be 28 °C and a pH of 6. The ITS1, 5.8S rRNA and D1, D2 domain of LSU rRNA gene characterization of the isolate CSR illustrated that it belongs to Ustilago genera. The isolate was deposited in NCBI GenBank as Ustilago sp. CSR (KY284846). Although, Ustilago is generally a pathogenic fungus, our study opens up the scope of using Ustilago spp. for bioremediation of the carcinogenic heavy metal Chromium. |
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−1
Cr (VI), determined by Atomic Absorption Spectroscopy (AAS) and DPC analysis. The most tolerant isolate designated as CSR was used for in vitro and ex-situ bioremediation studies of Cr (VI). The isolate achieved significant bioremediation of 86% in vitro and 75.12% in ex-situ method. The optimal conditions for in vitro bioremediation were found to be 28 °C and a pH of 6. The ITS1, 5.8S rRNA and D1, D2 domain of LSU rRNA gene characterization of the isolate CSR illustrated that it belongs to Ustilago genera. The isolate was deposited in NCBI GenBank as Ustilago sp. CSR (KY284846). Although, Ustilago is generally a pathogenic fungus, our study opens up the scope of using Ustilago spp. for bioremediation of the carcinogenic heavy metal Chromium.</description><identifier>ISSN: 1082-6068</identifier><identifier>EISSN: 1532-2297</identifier><identifier>DOI: 10.1080/10826068.2020.1755868</identifier><identifier>PMID: 32302260</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Atomic absorption analysis ; Atomic absorption spectroscopy ; Atomic beam spectroscopy ; Biodegradation, Environmental ; Bioremediation ; Carcinogens ; Carcinogens - isolation & purification ; Carcinogens - metabolism ; Chromium ; Chromium - isolation & purification ; Chromium - metabolism ; diphenylcarbazide analysis ; energy dispersion x-ray analysis ; Fungi ; Heavy metals ; Hexavalent chromium ; Humans ; indigenous yeast ; Pollutants ; rRNA ; rRNA 5.8S ; Sediment pollution ; Soil Microbiology ; Soil Pollutants - isolation & purification ; Soil Pollutants - metabolism ; Soil pollution ; Soil remediation ; Spectral analysis ; Ustilago ; Yeasts ; Yeasts - isolation & purification ; Yeasts - metabolism</subject><ispartof>Preparative biochemistry & biotechnology, 2020-09, Vol.50 (8), p.842-848</ispartof><rights>2020 Taylor & Francis Group, LLC 2020</rights><rights>2020 Taylor & Francis Group, LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c309t-2013f3a11a1a930d51d467c66c90fd0dab5b1c97a04e43a817fb963fcbd8ec993</citedby><cites>FETCH-LOGICAL-c309t-2013f3a11a1a930d51d467c66c90fd0dab5b1c97a04e43a817fb963fcbd8ec993</cites><orcidid>0000-0002-6327-1452</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32302260$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kamarudheen, Neethu</creatorcontrib><creatorcontrib>Chacko, Sona P.</creatorcontrib><creatorcontrib>George, Catherin A.</creatorcontrib><creatorcontrib>Chettiparambil Somachandran, Rakhi</creatorcontrib><creatorcontrib>Rao, K. V. Bhaskara</creatorcontrib><title>An ex-situ and in vitro approach towards the bioremediation of carcinogenic hexavalent chromium</title><title>Preparative biochemistry & biotechnology</title><addtitle>Prep Biochem Biotechnol</addtitle><description>Chromium, ranking the second most among toxic heavy metal pollutants in the world, causing respiratory, cardiovascular and renal problems in human beings is under study herein. We examined the biological remediation of the carcinogenic Cr (VI) polluted soils by indigenous yeast isolates. The total element analysis of the treated sample was determined by Energy Dispersion X-ray Micro Analysis (EDXMA). The sample under study was observed to have a high concentration of 458.29 mgKg
−1
Cr (VI), determined by Atomic Absorption Spectroscopy (AAS) and DPC analysis. The most tolerant isolate designated as CSR was used for in vitro and ex-situ bioremediation studies of Cr (VI). The isolate achieved significant bioremediation of 86% in vitro and 75.12% in ex-situ method. The optimal conditions for in vitro bioremediation were found to be 28 °C and a pH of 6. The ITS1, 5.8S rRNA and D1, D2 domain of LSU rRNA gene characterization of the isolate CSR illustrated that it belongs to Ustilago genera. The isolate was deposited in NCBI GenBank as Ustilago sp. CSR (KY284846). Although, Ustilago is generally a pathogenic fungus, our study opens up the scope of using Ustilago spp. for bioremediation of the carcinogenic heavy metal Chromium.</description><subject>Atomic absorption analysis</subject><subject>Atomic absorption spectroscopy</subject><subject>Atomic beam spectroscopy</subject><subject>Biodegradation, Environmental</subject><subject>Bioremediation</subject><subject>Carcinogens</subject><subject>Carcinogens - isolation & purification</subject><subject>Carcinogens - metabolism</subject><subject>Chromium</subject><subject>Chromium - isolation & purification</subject><subject>Chromium - metabolism</subject><subject>diphenylcarbazide analysis</subject><subject>energy dispersion x-ray analysis</subject><subject>Fungi</subject><subject>Heavy metals</subject><subject>Hexavalent chromium</subject><subject>Humans</subject><subject>indigenous yeast</subject><subject>Pollutants</subject><subject>rRNA</subject><subject>rRNA 5.8S</subject><subject>Sediment pollution</subject><subject>Soil Microbiology</subject><subject>Soil Pollutants - isolation & purification</subject><subject>Soil Pollutants - metabolism</subject><subject>Soil pollution</subject><subject>Soil remediation</subject><subject>Spectral analysis</subject><subject>Ustilago</subject><subject>Yeasts</subject><subject>Yeasts - isolation & purification</subject><subject>Yeasts - metabolism</subject><issn>1082-6068</issn><issn>1532-2297</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kMlOBCEQhonRuD-ChsRzK8v0wk1j3BITL3rGahYHMw0j0I6-jc_ik8lkRo9eKEK-v4r6EDqi5JSSjpyVgzWk6U4ZYeWpreuu6TbQLq05qxgT7Wa5F6ZaQjtoL6VXQqhoabeNdjjjhJX4Lnq-8Nh8VMnlEYPX2Pnvr3eXY8Awn8cAaopzWEDUCeepwb0L0QxGO8gueBwsVhCV8-HFeKfw1HzAO8yMz1hNYxjcOBygLQuzZA7XdR89XV89Xt5W9w83d5cX95XiROSKEcotB0qBguBE11RPmlY1jRLEaqKhr3uqRAtkYiYcOtraXjTcql53RgnB99HJqm_59dtoUpavYYy-jJRswgXjgjdLql5RKoaUorFyHt0A8VNSIpde5a9XufQq115L7njdfezL-n-pX5EFOF8BztsQB1iEONMyw-csRBvBK5ck_3_GD57riNg</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Kamarudheen, Neethu</creator><creator>Chacko, Sona P.</creator><creator>George, Catherin A.</creator><creator>Chettiparambil Somachandran, Rakhi</creator><creator>Rao, K. V. Bhaskara</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><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>7QL</scope><scope>7QO</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0002-6327-1452</orcidid></search><sort><creationdate>20200901</creationdate><title>An ex-situ and in vitro approach towards the bioremediation of carcinogenic hexavalent chromium</title><author>Kamarudheen, Neethu ; Chacko, Sona P. ; George, Catherin A. ; Chettiparambil Somachandran, Rakhi ; Rao, K. V. Bhaskara</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-2013f3a11a1a930d51d467c66c90fd0dab5b1c97a04e43a817fb963fcbd8ec993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Atomic absorption analysis</topic><topic>Atomic absorption spectroscopy</topic><topic>Atomic beam spectroscopy</topic><topic>Biodegradation, Environmental</topic><topic>Bioremediation</topic><topic>Carcinogens</topic><topic>Carcinogens - isolation & purification</topic><topic>Carcinogens - metabolism</topic><topic>Chromium</topic><topic>Chromium - isolation & purification</topic><topic>Chromium - metabolism</topic><topic>diphenylcarbazide analysis</topic><topic>energy dispersion x-ray analysis</topic><topic>Fungi</topic><topic>Heavy metals</topic><topic>Hexavalent chromium</topic><topic>Humans</topic><topic>indigenous yeast</topic><topic>Pollutants</topic><topic>rRNA</topic><topic>rRNA 5.8S</topic><topic>Sediment pollution</topic><topic>Soil Microbiology</topic><topic>Soil Pollutants - isolation & purification</topic><topic>Soil Pollutants - metabolism</topic><topic>Soil pollution</topic><topic>Soil remediation</topic><topic>Spectral analysis</topic><topic>Ustilago</topic><topic>Yeasts</topic><topic>Yeasts - isolation & purification</topic><topic>Yeasts - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kamarudheen, Neethu</creatorcontrib><creatorcontrib>Chacko, Sona P.</creatorcontrib><creatorcontrib>George, Catherin A.</creatorcontrib><creatorcontrib>Chettiparambil Somachandran, Rakhi</creatorcontrib><creatorcontrib>Rao, K. 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V. Bhaskara</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An ex-situ and in vitro approach towards the bioremediation of carcinogenic hexavalent chromium</atitle><jtitle>Preparative biochemistry & biotechnology</jtitle><addtitle>Prep Biochem Biotechnol</addtitle><date>2020-09-01</date><risdate>2020</risdate><volume>50</volume><issue>8</issue><spage>842</spage><epage>848</epage><pages>842-848</pages><issn>1082-6068</issn><eissn>1532-2297</eissn><abstract>Chromium, ranking the second most among toxic heavy metal pollutants in the world, causing respiratory, cardiovascular and renal problems in human beings is under study herein. We examined the biological remediation of the carcinogenic Cr (VI) polluted soils by indigenous yeast isolates. The total element analysis of the treated sample was determined by Energy Dispersion X-ray Micro Analysis (EDXMA). The sample under study was observed to have a high concentration of 458.29 mgKg
−1
Cr (VI), determined by Atomic Absorption Spectroscopy (AAS) and DPC analysis. The most tolerant isolate designated as CSR was used for in vitro and ex-situ bioremediation studies of Cr (VI). The isolate achieved significant bioremediation of 86% in vitro and 75.12% in ex-situ method. The optimal conditions for in vitro bioremediation were found to be 28 °C and a pH of 6. The ITS1, 5.8S rRNA and D1, D2 domain of LSU rRNA gene characterization of the isolate CSR illustrated that it belongs to Ustilago genera. The isolate was deposited in NCBI GenBank as Ustilago sp. CSR (KY284846). Although, Ustilago is generally a pathogenic fungus, our study opens up the scope of using Ustilago spp. for bioremediation of the carcinogenic heavy metal Chromium.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>32302260</pmid><doi>10.1080/10826068.2020.1755868</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6327-1452</orcidid></addata></record> |
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subjects | Atomic absorption analysis Atomic absorption spectroscopy Atomic beam spectroscopy Biodegradation, Environmental Bioremediation Carcinogens Carcinogens - isolation & purification Carcinogens - metabolism Chromium Chromium - isolation & purification Chromium - metabolism diphenylcarbazide analysis energy dispersion x-ray analysis Fungi Heavy metals Hexavalent chromium Humans indigenous yeast Pollutants rRNA rRNA 5.8S Sediment pollution Soil Microbiology Soil Pollutants - isolation & purification Soil Pollutants - metabolism Soil pollution Soil remediation Spectral analysis Ustilago Yeasts Yeasts - isolation & purification Yeasts - metabolism |
title | An ex-situ and in vitro approach towards the bioremediation of carcinogenic hexavalent chromium |
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