Enzyme activities of aerobic lignocellulolytic bacteria isolated from wet tropical forest soils
Lignocellulolytic bacteria have promised to be a fruitful source of new enzymes for next-generation lignocellulosic biofuel production. Puerto Rican tropical forest soils were targeted because the resident microbes decompose biomass quickly and to near-completion. Isolates were initially screened ba...
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description | Lignocellulolytic bacteria have promised to be a fruitful source of new enzymes for next-generation lignocellulosic biofuel production. Puerto Rican tropical forest soils were targeted because the resident microbes decompose biomass quickly and to near-completion. Isolates were initially screened based on growth on cellulose or lignin in minimal media. 75 Isolates were further tested for the following lignocellulolytic enzyme activities: phenol oxidase, peroxidase, β-d-glucosidase, cellobiohydrolase, β-xylopyranosidase, chitinase, CMCase, and xylanase. Cellulose-derived isolates possessed elevated β-d-glucosidase, CMCase, and cellobiohydrolase activity but depressed phenol oxidase and peroxidase activity, while the contrary was true of lignin isolates, suggesting that these bacteria are specialized to subsist on cellulose or lignin. Cellobiohydrolase and phenol oxidase activity rates could classify lignin and cellulose isolates with 61% accuracy, which demonstrates the utility of model degradation assays. Based on 16S rRNA gene sequencing, all isolates belonged to phyla dominant in the Puerto Rican soils, Proteobacteria, Firmicutes, and Actinobacteria, suggesting that many dominant taxa are capable of the rapid lignocellulose degradation characteristic of these soils. The isolated genera Aquitalea, Bacillus, Burkholderia, Cupriavidus, Gordonia, and Paenibacillus represent rarely or never before studied lignolytic or cellulolytic species and were undetected by metagenomic analysis of the soils. The study revealed a relationship between phylogeny and lignocellulose-degrading potential, supported by Kruskal–Wallis statistics which showed that enzyme activities of cultivated phyla and genera were different enough to be considered representatives of distinct populations. This can better inform future experiments and enzyme discovery efforts. |
doi_str_mv | 10.1016/j.syapm.2013.10.001 |
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Puerto Rican tropical forest soils were targeted because the resident microbes decompose biomass quickly and to near-completion. Isolates were initially screened based on growth on cellulose or lignin in minimal media. 75 Isolates were further tested for the following lignocellulolytic enzyme activities: phenol oxidase, peroxidase, β-d-glucosidase, cellobiohydrolase, β-xylopyranosidase, chitinase, CMCase, and xylanase. Cellulose-derived isolates possessed elevated β-d-glucosidase, CMCase, and cellobiohydrolase activity but depressed phenol oxidase and peroxidase activity, while the contrary was true of lignin isolates, suggesting that these bacteria are specialized to subsist on cellulose or lignin. Cellobiohydrolase and phenol oxidase activity rates could classify lignin and cellulose isolates with 61% accuracy, which demonstrates the utility of model degradation assays. Based on 16S rRNA gene sequencing, all isolates belonged to phyla dominant in the Puerto Rican soils, Proteobacteria, Firmicutes, and Actinobacteria, suggesting that many dominant taxa are capable of the rapid lignocellulose degradation characteristic of these soils. The isolated genera Aquitalea, Bacillus, Burkholderia, Cupriavidus, Gordonia, and Paenibacillus represent rarely or never before studied lignolytic or cellulolytic species and were undetected by metagenomic analysis of the soils. The study revealed a relationship between phylogeny and lignocellulose-degrading potential, supported by Kruskal–Wallis statistics which showed that enzyme activities of cultivated phyla and genera were different enough to be considered representatives of distinct populations. This can better inform future experiments and enzyme discovery efforts.</description><identifier>ISSN: 0723-2020</identifier><identifier>EISSN: 1618-0984</identifier><identifier>DOI: 10.1016/j.syapm.2013.10.001</identifier><identifier>PMID: 24238986</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Aerobiosis ; Bacteria - classification ; Bacteria - enzymology ; Bacteria - isolation & purification ; Bacteria - metabolism ; Biodiversity ; Biofuels ; Biomass degradation ; Cellulose ; Cluster Analysis ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; DNA, Ribosomal - chemistry ; DNA, Ribosomal - genetics ; Enzymes - analysis ; Lignin ; Lignin - metabolism ; Molecular Sequence Data ; Phylogeny ; Puerto Rico ; RNA, Ribosomal, 16S - genetics ; Sequence Analysis, DNA ; Soil lignocellulolytic bacteria ; Soil Microbiology ; Trees ; Tropical forest</subject><ispartof>Systematic and applied microbiology, 2014-02, Vol.37 (1), p.60-67</ispartof><rights>2013 Elsevier GmbH</rights><rights>Copyright © 2013 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-c109e29151d1082f5a0d45c31e2117f6c69d299b6fdcfd88f2d547074212abdb3</citedby><cites>FETCH-LOGICAL-c431t-c109e29151d1082f5a0d45c31e2117f6c69d299b6fdcfd88f2d547074212abdb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.syapm.2013.10.001$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24238986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1153270$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Woo, Hannah L.</creatorcontrib><creatorcontrib>Hazen, Terry C.</creatorcontrib><creatorcontrib>Simmons, Blake A.</creatorcontrib><creatorcontrib>DeAngelis, Kristen M.</creatorcontrib><creatorcontrib>Joint Bioenergy Institute (JBEI)</creatorcontrib><title>Enzyme activities of aerobic lignocellulolytic bacteria isolated from wet tropical forest soils</title><title>Systematic and applied microbiology</title><addtitle>Syst Appl Microbiol</addtitle><description>Lignocellulolytic bacteria have promised to be a fruitful source of new enzymes for next-generation lignocellulosic biofuel production. Puerto Rican tropical forest soils were targeted because the resident microbes decompose biomass quickly and to near-completion. Isolates were initially screened based on growth on cellulose or lignin in minimal media. 75 Isolates were further tested for the following lignocellulolytic enzyme activities: phenol oxidase, peroxidase, β-d-glucosidase, cellobiohydrolase, β-xylopyranosidase, chitinase, CMCase, and xylanase. Cellulose-derived isolates possessed elevated β-d-glucosidase, CMCase, and cellobiohydrolase activity but depressed phenol oxidase and peroxidase activity, while the contrary was true of lignin isolates, suggesting that these bacteria are specialized to subsist on cellulose or lignin. Cellobiohydrolase and phenol oxidase activity rates could classify lignin and cellulose isolates with 61% accuracy, which demonstrates the utility of model degradation assays. Based on 16S rRNA gene sequencing, all isolates belonged to phyla dominant in the Puerto Rican soils, Proteobacteria, Firmicutes, and Actinobacteria, suggesting that many dominant taxa are capable of the rapid lignocellulose degradation characteristic of these soils. The isolated genera Aquitalea, Bacillus, Burkholderia, Cupriavidus, Gordonia, and Paenibacillus represent rarely or never before studied lignolytic or cellulolytic species and were undetected by metagenomic analysis of the soils. The study revealed a relationship between phylogeny and lignocellulose-degrading potential, supported by Kruskal–Wallis statistics which showed that enzyme activities of cultivated phyla and genera were different enough to be considered representatives of distinct populations. This can better inform future experiments and enzyme discovery efforts.</description><subject>Aerobiosis</subject><subject>Bacteria - classification</subject><subject>Bacteria - enzymology</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteria - metabolism</subject><subject>Biodiversity</subject><subject>Biofuels</subject><subject>Biomass degradation</subject><subject>Cellulose</subject><subject>Cluster Analysis</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Ribosomal - chemistry</subject><subject>DNA, Ribosomal - genetics</subject><subject>Enzymes - analysis</subject><subject>Lignin</subject><subject>Lignin - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Phylogeny</subject><subject>Puerto Rico</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>Soil lignocellulolytic bacteria</subject><subject>Soil Microbiology</subject><subject>Trees</subject><subject>Tropical forest</subject><issn>0723-2020</issn><issn>1618-0984</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1vVCEUhomxsdPqLzAxxJWbO3KA-7VwYZq2mjRxU9eECwdlwr2MwLQZf73cTnXpiuTNczjveQh5C2wLDLqPu20-6v285QxETbaMwQuygQ6Gho2DfEk2rOei4Yyzc3KR864CcuzgFTnnkothHLoNUdfL7-OMVJviH3zxmGl0VGOKkzc0-B9LNBjCIcRwLDWZKojJa-pzDLqgpS7FmT5ioSXFvTc6UBcT5kJz9CG_JmdOh4xvnt9L8v3m-v7qS3P37fbr1ee7xkgBpTHARuQjtGCBDdy1mlnZGgHIAXrXmW60fBynzlnj7DA4blvZs15y4Hqyk7gk70__xly8ysYXND9NXBY0RQG0gvesQh9O0D7FX4faUc0-r-fpBeMhq6pHCsY7kBUVJ9SkmHNCp_bJzzodFTC16lc79aRfrfrXsNqtU--eFxymGe2_mb--K_DpBGB18eAxrVVxMWh9Wpva6P-74A8V5Zgf</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Woo, Hannah L.</creator><creator>Hazen, Terry C.</creator><creator>Simmons, Blake A.</creator><creator>DeAngelis, Kristen M.</creator><general>Elsevier GmbH</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>201402</creationdate><title>Enzyme activities of aerobic lignocellulolytic bacteria isolated from wet tropical forest soils</title><author>Woo, Hannah L. ; Hazen, Terry C. ; Simmons, Blake A. ; DeAngelis, Kristen M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-c109e29151d1082f5a0d45c31e2117f6c69d299b6fdcfd88f2d547074212abdb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aerobiosis</topic><topic>Bacteria - classification</topic><topic>Bacteria - enzymology</topic><topic>Bacteria - isolation & purification</topic><topic>Bacteria - metabolism</topic><topic>Biodiversity</topic><topic>Biofuels</topic><topic>Biomass degradation</topic><topic>Cellulose</topic><topic>Cluster Analysis</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Ribosomal - chemistry</topic><topic>DNA, Ribosomal - genetics</topic><topic>Enzymes - analysis</topic><topic>Lignin</topic><topic>Lignin - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Phylogeny</topic><topic>Puerto Rico</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>Soil lignocellulolytic bacteria</topic><topic>Soil Microbiology</topic><topic>Trees</topic><topic>Tropical forest</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woo, Hannah L.</creatorcontrib><creatorcontrib>Hazen, Terry C.</creatorcontrib><creatorcontrib>Simmons, Blake A.</creatorcontrib><creatorcontrib>DeAngelis, Kristen M.</creatorcontrib><creatorcontrib>Joint Bioenergy Institute (JBEI)</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Systematic and applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woo, Hannah L.</au><au>Hazen, Terry C.</au><au>Simmons, Blake A.</au><au>DeAngelis, Kristen M.</au><aucorp>Joint Bioenergy Institute (JBEI)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzyme activities of aerobic lignocellulolytic bacteria isolated from wet tropical forest soils</atitle><jtitle>Systematic and applied microbiology</jtitle><addtitle>Syst Appl Microbiol</addtitle><date>2014-02</date><risdate>2014</risdate><volume>37</volume><issue>1</issue><spage>60</spage><epage>67</epage><pages>60-67</pages><issn>0723-2020</issn><eissn>1618-0984</eissn><abstract>Lignocellulolytic bacteria have promised to be a fruitful source of new enzymes for next-generation lignocellulosic biofuel production. Puerto Rican tropical forest soils were targeted because the resident microbes decompose biomass quickly and to near-completion. Isolates were initially screened based on growth on cellulose or lignin in minimal media. 75 Isolates were further tested for the following lignocellulolytic enzyme activities: phenol oxidase, peroxidase, β-d-glucosidase, cellobiohydrolase, β-xylopyranosidase, chitinase, CMCase, and xylanase. Cellulose-derived isolates possessed elevated β-d-glucosidase, CMCase, and cellobiohydrolase activity but depressed phenol oxidase and peroxidase activity, while the contrary was true of lignin isolates, suggesting that these bacteria are specialized to subsist on cellulose or lignin. Cellobiohydrolase and phenol oxidase activity rates could classify lignin and cellulose isolates with 61% accuracy, which demonstrates the utility of model degradation assays. Based on 16S rRNA gene sequencing, all isolates belonged to phyla dominant in the Puerto Rican soils, Proteobacteria, Firmicutes, and Actinobacteria, suggesting that many dominant taxa are capable of the rapid lignocellulose degradation characteristic of these soils. The isolated genera Aquitalea, Bacillus, Burkholderia, Cupriavidus, Gordonia, and Paenibacillus represent rarely or never before studied lignolytic or cellulolytic species and were undetected by metagenomic analysis of the soils. The study revealed a relationship between phylogeny and lignocellulose-degrading potential, supported by Kruskal–Wallis statistics which showed that enzyme activities of cultivated phyla and genera were different enough to be considered representatives of distinct populations. This can better inform future experiments and enzyme discovery efforts.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>24238986</pmid><doi>10.1016/j.syapm.2013.10.001</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aerobiosis Bacteria - classification Bacteria - enzymology Bacteria - isolation & purification Bacteria - metabolism Biodiversity Biofuels Biomass degradation Cellulose Cluster Analysis DNA, Bacterial - chemistry DNA, Bacterial - genetics DNA, Ribosomal - chemistry DNA, Ribosomal - genetics Enzymes - analysis Lignin Lignin - metabolism Molecular Sequence Data Phylogeny Puerto Rico RNA, Ribosomal, 16S - genetics Sequence Analysis, DNA Soil lignocellulolytic bacteria Soil Microbiology Trees Tropical forest |
title | Enzyme activities of aerobic lignocellulolytic bacteria isolated from wet tropical forest soils |
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