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Molecular Detection of Penicillium griseofulvum as the Coastal Pollution Indicator
Molecular methods were carried out to detect Penicillium griseofulvum, a dominant species related to heavy metal pollution, which was screened from marine contaminated sediments. Based on differences in internal transcribed spacer (ITS) sequences of Penicillium genus and specific isoamyl alcohol oxi...
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Published in: | Current microbiology 2011-02, Vol.62 (2), p.396-401 |
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description | Molecular methods were carried out to detect Penicillium griseofulvum, a dominant species related to heavy metal pollution, which was screened from marine contaminated sediments. Based on differences in internal transcribed spacer (ITS) sequences of Penicillium genus and specific isoamyl alcohol oxidase (IAO) sequences, species-specific primers AS1/RS4 and IAO1/IAO2 of Penicillium griseofulvum were designed and synthesized which were then employed in optimized PCR systems. The detection sensitivities were compared through ordinary PCR and nested-PCR using two pairs of primers, respectively. Both primer pairs could exclusively amplify destined DNA fragment from contaminated environmental samples in our researches. As for primers AS1/RS4, the detection sensitivity for spores (pure spore DNA) could be 10 fg/μl and 10 spores, respectively, and the detection sensitivity for the sediments was 10² spores/0.25 g sediments. While the detection sensitivity of IAO1/IAO2 primers was lower than that of AS1/RS4. Despite the difference in detection sensitivity, it is feasible that the species-specific primers could be used as probes for the detection of environmental pollution dominant species, Penicillium griseofulvum, since the frequency of occurrence and amount of this strain could preferably indicate the pollution degree. |
doi_str_mv | 10.1007/s00284-010-9720-4 |
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Based on differences in internal transcribed spacer (ITS) sequences of Penicillium genus and specific isoamyl alcohol oxidase (IAO) sequences, species-specific primers AS1/RS4 and IAO1/IAO2 of Penicillium griseofulvum were designed and synthesized which were then employed in optimized PCR systems. The detection sensitivities were compared through ordinary PCR and nested-PCR using two pairs of primers, respectively. Both primer pairs could exclusively amplify destined DNA fragment from contaminated environmental samples in our researches. As for primers AS1/RS4, the detection sensitivity for spores (pure spore DNA) could be 10 fg/μl and 10 spores, respectively, and the detection sensitivity for the sediments was 10² spores/0.25 g sediments. While the detection sensitivity of IAO1/IAO2 primers was lower than that of AS1/RS4. Despite the difference in detection sensitivity, it is feasible that the species-specific primers could be used as probes for the detection of environmental pollution dominant species, Penicillium griseofulvum, since the frequency of occurrence and amount of this strain could preferably indicate the pollution degree.</description><identifier>ISSN: 0343-8651</identifier><identifier>EISSN: 1432-0991</identifier><identifier>DOI: 10.1007/s00284-010-9720-4</identifier><identifier>PMID: 20658343</identifier><language>eng</language><publisher>New York: New York : Springer-Verlag</publisher><subject>Biomedical and Life Sciences ; Biotechnology ; Coasts ; Contaminated sediments ; Deoxyribonucleic acid ; DNA ; DNA Primers - genetics ; DNA, Fungal - genetics ; DNA, Ribosomal Spacer - genetics ; Dominant species ; Environmental indicators ; Environmental Pollutants - metabolism ; Environmental Pollution ; Fungal Proteins - genetics ; Geologic Sediments - microbiology ; Heavy metals ; Life Sciences ; Marine pollution ; Metals, Heavy - metabolism ; Microbiology ; Molecular biology ; Mycology - methods ; Oxidoreductases - genetics ; Penicillium - genetics ; Penicillium - isolation & purification ; Pollution detection ; Polymerase Chain Reaction - methods ; Sediment pollution ; Sediments ; Sensitivity and Specificity ; Soil contamination</subject><ispartof>Current microbiology, 2011-02, Vol.62 (2), p.396-401</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><rights>Springer Science+Business Media, LLC 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-a2a5a6dbb146868acd493ef9fcd2116330fd1d8052acab1a7a0753b230e383bf3</citedby><cites>FETCH-LOGICAL-c426t-a2a5a6dbb146868acd493ef9fcd2116330fd1d8052acab1a7a0753b230e383bf3</cites></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/20658343$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Zhengping</creatorcontrib><creatorcontrib>Bai, Shumeng</creatorcontrib><creatorcontrib>Tian, Li</creatorcontrib><creatorcontrib>Jiang, Huichao</creatorcontrib><creatorcontrib>Zhang, Jiuming</creatorcontrib><title>Molecular Detection of Penicillium griseofulvum as the Coastal Pollution Indicator</title><title>Current microbiology</title><addtitle>Curr Microbiol</addtitle><addtitle>Curr Microbiol</addtitle><description>Molecular methods were carried out to detect Penicillium griseofulvum, a dominant species related to heavy metal pollution, which was screened from marine contaminated sediments. Based on differences in internal transcribed spacer (ITS) sequences of Penicillium genus and specific isoamyl alcohol oxidase (IAO) sequences, species-specific primers AS1/RS4 and IAO1/IAO2 of Penicillium griseofulvum were designed and synthesized which were then employed in optimized PCR systems. The detection sensitivities were compared through ordinary PCR and nested-PCR using two pairs of primers, respectively. Both primer pairs could exclusively amplify destined DNA fragment from contaminated environmental samples in our researches. As for primers AS1/RS4, the detection sensitivity for spores (pure spore DNA) could be 10 fg/μl and 10 spores, respectively, and the detection sensitivity for the sediments was 10² spores/0.25 g sediments. While the detection sensitivity of IAO1/IAO2 primers was lower than that of AS1/RS4. Despite the difference in detection sensitivity, it is feasible that the species-specific primers could be used as probes for the detection of environmental pollution dominant species, Penicillium griseofulvum, since the frequency of occurrence and amount of this strain could preferably indicate the pollution degree.</description><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Coasts</subject><subject>Contaminated sediments</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Primers - genetics</subject><subject>DNA, Fungal - genetics</subject><subject>DNA, Ribosomal Spacer - genetics</subject><subject>Dominant species</subject><subject>Environmental indicators</subject><subject>Environmental Pollutants - metabolism</subject><subject>Environmental Pollution</subject><subject>Fungal Proteins - genetics</subject><subject>Geologic Sediments - microbiology</subject><subject>Heavy metals</subject><subject>Life Sciences</subject><subject>Marine pollution</subject><subject>Metals, Heavy - metabolism</subject><subject>Microbiology</subject><subject>Molecular biology</subject><subject>Mycology - methods</subject><subject>Oxidoreductases - genetics</subject><subject>Penicillium - genetics</subject><subject>Penicillium - isolation & purification</subject><subject>Pollution detection</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Sediment pollution</subject><subject>Sediments</subject><subject>Sensitivity and Specificity</subject><subject>Soil 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Detection of Penicillium griseofulvum as the Coastal Pollution Indicator</title><author>Shi, Zhengping ; Bai, Shumeng ; Tian, Li ; Jiang, Huichao ; Zhang, Jiuming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-a2a5a6dbb146868acd493ef9fcd2116330fd1d8052acab1a7a0753b230e383bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Coasts</topic><topic>Contaminated sediments</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Primers - genetics</topic><topic>DNA, Fungal - genetics</topic><topic>DNA, Ribosomal Spacer - genetics</topic><topic>Dominant species</topic><topic>Environmental indicators</topic><topic>Environmental Pollutants - metabolism</topic><topic>Environmental Pollution</topic><topic>Fungal Proteins - genetics</topic><topic>Geologic Sediments - 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Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Current microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Zhengping</au><au>Bai, Shumeng</au><au>Tian, Li</au><au>Jiang, Huichao</au><au>Zhang, Jiuming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Detection of Penicillium griseofulvum as the Coastal Pollution Indicator</atitle><jtitle>Current microbiology</jtitle><stitle>Curr Microbiol</stitle><addtitle>Curr Microbiol</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>62</volume><issue>2</issue><spage>396</spage><epage>401</epage><pages>396-401</pages><issn>0343-8651</issn><eissn>1432-0991</eissn><abstract>Molecular methods were carried out to detect Penicillium griseofulvum, a dominant species related to heavy metal pollution, which was screened from marine contaminated sediments. Based on differences in internal transcribed spacer (ITS) sequences of Penicillium genus and specific isoamyl alcohol oxidase (IAO) sequences, species-specific primers AS1/RS4 and IAO1/IAO2 of Penicillium griseofulvum were designed and synthesized which were then employed in optimized PCR systems. The detection sensitivities were compared through ordinary PCR and nested-PCR using two pairs of primers, respectively. Both primer pairs could exclusively amplify destined DNA fragment from contaminated environmental samples in our researches. As for primers AS1/RS4, the detection sensitivity for spores (pure spore DNA) could be 10 fg/μl and 10 spores, respectively, and the detection sensitivity for the sediments was 10² spores/0.25 g sediments. While the detection sensitivity of IAO1/IAO2 primers was lower than that of AS1/RS4. Despite the difference in detection sensitivity, it is feasible that the species-specific primers could be used as probes for the detection of environmental pollution dominant species, Penicillium griseofulvum, since the frequency of occurrence and amount of this strain could preferably indicate the pollution degree.</abstract><cop>New York</cop><pub>New York : Springer-Verlag</pub><pmid>20658343</pmid><doi>10.1007/s00284-010-9720-4</doi><tpages>6</tpages></addata></record> |
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subjects | Biomedical and Life Sciences Biotechnology Coasts Contaminated sediments Deoxyribonucleic acid DNA DNA Primers - genetics DNA, Fungal - genetics DNA, Ribosomal Spacer - genetics Dominant species Environmental indicators Environmental Pollutants - metabolism Environmental Pollution Fungal Proteins - genetics Geologic Sediments - microbiology Heavy metals Life Sciences Marine pollution Metals, Heavy - metabolism Microbiology Molecular biology Mycology - methods Oxidoreductases - genetics Penicillium - genetics Penicillium - isolation & purification Pollution detection Polymerase Chain Reaction - methods Sediment pollution Sediments Sensitivity and Specificity Soil contamination |
title | Molecular Detection of Penicillium griseofulvum as the Coastal Pollution Indicator |
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