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Comprehensive enzymatic analysis of the cellulolytic system in digestive fluid of the Sea Hare Aplysia kurodai. Efficient glucose release from sea lettuce by synergistic action of 45 kDa endoglucanase and 210 kDa ß-glucosidase
Although many endo-ß-1,4-glucanases have been isolated in invertebrates, their cellulolytic systems are not fully understood. In particular, gastropod feeding on seaweed is considered an excellent model system for production of bioethanol and renewable bioenergy from third-generation feedstocks (mic...
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Published in: | PloS one 2013-06, Vol.8 (6), p.e65418-e65418 |
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description | Although many endo-ß-1,4-glucanases have been isolated in invertebrates, their cellulolytic systems are not fully understood. In particular, gastropod feeding on seaweed is considered an excellent model system for production of bioethanol and renewable bioenergy from third-generation feedstocks (microalgae and seaweeds). In this study, enzymes involved in the conversion of cellulose and other polysaccharides to glucose in digestive fluids of the sea hare (Aplysia kurodai) were screened and characterized to determine how the sea hare obtains glucose from sea lettuce (Ulva pertusa). Four endo-ß-1,4-glucanases (21K, 45K, 65K, and 95K cellulase) and 2 ß-glucosidases (110K and 210K) were purified to a homogeneous state, and the synergistic action of these enzymes during cellulose digestion was analyzed. All cellulases exhibited cellulase and lichenase activities and showed distinct cleavage specificities against cellooligosaccharides and filter paper. Filter paper was digested to cellobiose, cellotriose, and cellotetraose by 21K cellulase, whereas 45K and 65K enzymes hydrolyzed the filter paper to cellobiose and glucose. 210K ß-glucosidase showed unique substrate specificity against synthetic and natural substrates, and 4-methylumbelliferyl (4MU)-ß-glucoside, 4MU-ß-galactoside, cello-oligosaccharides, laminarin, and lichenan were suitable substrates. Furthermore, 210K ß-glucosidase possesses lactase activity. Although ß-glucosidase and cellulase are necessary for efficient hydrolysis of carboxymethylcellulose to glucose, laminarin is hydrolyzed to glucose only by 210K ß-glucosidase. Kinetic analysis of the inhibition of 210K ß-glucosidase by D-glucono-1,5-lactone suggested the presence of 2 active sites similar to those of mammalian lactase-phlorizin hydrolase. Saccharification of sea lettuce was considerably stimulated by the synergistic action of 45K cellulase and 210K ß-glucosidase. Our results indicate that 45K cellulase and 210K ß-glucosidase are the core components of the sea hare digestive system for efficient production of glucose from sea lettuce. These findings contribute important new insights into the development of biofuel processing biotechnologies from seaweed. |
doi_str_mv | 10.1371/journal.pone.0065418 |
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Efficient glucose release from sea lettuce by synergistic action of 45 kDa endoglucanase and 210 kDa ß-glucosidase</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Tsuji, Akihiko ; Tominaga, Keiko ; Nishiyama, Nami ; Yuasa, Keizo</creator><contributor>Sanchez-Ruiz, Jose M.</contributor><creatorcontrib>Tsuji, Akihiko ; Tominaga, Keiko ; Nishiyama, Nami ; Yuasa, Keizo ; Sanchez-Ruiz, Jose M.</creatorcontrib><description>Although many endo-ß-1,4-glucanases have been isolated in invertebrates, their cellulolytic systems are not fully understood. In particular, gastropod feeding on seaweed is considered an excellent model system for production of bioethanol and renewable bioenergy from third-generation feedstocks (microalgae and seaweeds). In this study, enzymes involved in the conversion of cellulose and other polysaccharides to glucose in digestive fluids of the sea hare (Aplysia kurodai) were screened and characterized to determine how the sea hare obtains glucose from sea lettuce (Ulva pertusa). Four endo-ß-1,4-glucanases (21K, 45K, 65K, and 95K cellulase) and 2 ß-glucosidases (110K and 210K) were purified to a homogeneous state, and the synergistic action of these enzymes during cellulose digestion was analyzed. All cellulases exhibited cellulase and lichenase activities and showed distinct cleavage specificities against cellooligosaccharides and filter paper. Filter paper was digested to cellobiose, cellotriose, and cellotetraose by 21K cellulase, whereas 45K and 65K enzymes hydrolyzed the filter paper to cellobiose and glucose. 210K ß-glucosidase showed unique substrate specificity against synthetic and natural substrates, and 4-methylumbelliferyl (4MU)-ß-glucoside, 4MU-ß-galactoside, cello-oligosaccharides, laminarin, and lichenan were suitable substrates. Furthermore, 210K ß-glucosidase possesses lactase activity. Although ß-glucosidase and cellulase are necessary for efficient hydrolysis of carboxymethylcellulose to glucose, laminarin is hydrolyzed to glucose only by 210K ß-glucosidase. Kinetic analysis of the inhibition of 210K ß-glucosidase by D-glucono-1,5-lactone suggested the presence of 2 active sites similar to those of mammalian lactase-phlorizin hydrolase. Saccharification of sea lettuce was considerably stimulated by the synergistic action of 45K cellulase and 210K ß-glucosidase. Our results indicate that 45K cellulase and 210K ß-glucosidase are the core components of the sea hare digestive system for efficient production of glucose from sea lettuce. These findings contribute important new insights into the development of biofuel processing biotechnologies from seaweed.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0065418</identifier><identifier>PMID: 23762366</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Agriculture ; Algae ; Amino Acid Sequence ; Amino acids ; Analysis ; Animals ; Aplysia ; Aplysia - enzymology ; Aquatic microorganisms ; Aquatic Organisms - enzymology ; beta-Glucosidase - chemistry ; beta-Glucosidase - isolation & purification ; beta-Glucosidase - metabolism ; Biodiesel fuels ; Biofuels ; Biology ; Biomass ; Biomass energy ; Carboxymethyl cellulose ; Carboxymethylcellulose ; Cellobiose ; Cellobiose - chemistry ; Cellobiose - metabolism ; Cellooligosaccharides ; Cellulase ; Cellulase - chemistry ; Cellulase - isolation & purification ; Cellulase - metabolism ; Cellulose ; Cellulose - analogs & derivatives ; Cellulose - chemistry ; Cellulose - metabolism ; Cloning ; Computational fluid dynamics ; Digestive system ; Endoglucanase ; Engineering ; Enzyme Assays ; Enzymes ; Ethanol ; Evolution & development ; Filter paper ; Gastrointestinal Tract - enzymology ; Glucans ; Gluconates - chemistry ; Glucose ; Glucose - metabolism ; Glucosidase ; Glucosides - chemistry ; Glucosides - metabolism ; Hydrolase ; Hydrolysis ; Invertebrates ; Kinetics ; Lactase ; Lactones - chemistry ; Laminarin ; Lettuce ; Lignin ; Lignocellulose ; Molecular Sequence Data ; Oligosaccharides ; Polysaccharides ; Polysaccharides - chemistry ; Polysaccharides - metabolism ; Proteins ; Raw materials ; Saccharides ; Saccharification ; Seaweeds ; Substrate Specificity ; Substrates ; Tetroses - chemistry ; Tetroses - metabolism ; Trichoderma reesei ; Ulva - chemistry</subject><ispartof>PloS one, 2013-06, Vol.8 (6), p.e65418-e65418</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Tsuji et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Tsuji et al 2013 Tsuji et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c7178-a14da5b27e90c33567b64d9cecff15672f470d8133b3283de96027bb281960ed3</citedby><cites>FETCH-LOGICAL-c7178-a14da5b27e90c33567b64d9cecff15672f470d8133b3283de96027bb281960ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1365653569/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1365653569?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23762366$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Sanchez-Ruiz, Jose M.</contributor><creatorcontrib>Tsuji, Akihiko</creatorcontrib><creatorcontrib>Tominaga, Keiko</creatorcontrib><creatorcontrib>Nishiyama, Nami</creatorcontrib><creatorcontrib>Yuasa, Keizo</creatorcontrib><title>Comprehensive enzymatic analysis of the cellulolytic system in digestive fluid of the Sea Hare Aplysia kurodai. Efficient glucose release from sea lettuce by synergistic action of 45 kDa endoglucanase and 210 kDa ß-glucosidase</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Although many endo-ß-1,4-glucanases have been isolated in invertebrates, their cellulolytic systems are not fully understood. In particular, gastropod feeding on seaweed is considered an excellent model system for production of bioethanol and renewable bioenergy from third-generation feedstocks (microalgae and seaweeds). In this study, enzymes involved in the conversion of cellulose and other polysaccharides to glucose in digestive fluids of the sea hare (Aplysia kurodai) were screened and characterized to determine how the sea hare obtains glucose from sea lettuce (Ulva pertusa). Four endo-ß-1,4-glucanases (21K, 45K, 65K, and 95K cellulase) and 2 ß-glucosidases (110K and 210K) were purified to a homogeneous state, and the synergistic action of these enzymes during cellulose digestion was analyzed. All cellulases exhibited cellulase and lichenase activities and showed distinct cleavage specificities against cellooligosaccharides and filter paper. Filter paper was digested to cellobiose, cellotriose, and cellotetraose by 21K cellulase, whereas 45K and 65K enzymes hydrolyzed the filter paper to cellobiose and glucose. 210K ß-glucosidase showed unique substrate specificity against synthetic and natural substrates, and 4-methylumbelliferyl (4MU)-ß-glucoside, 4MU-ß-galactoside, cello-oligosaccharides, laminarin, and lichenan were suitable substrates. Furthermore, 210K ß-glucosidase possesses lactase activity. Although ß-glucosidase and cellulase are necessary for efficient hydrolysis of carboxymethylcellulose to glucose, laminarin is hydrolyzed to glucose only by 210K ß-glucosidase. Kinetic analysis of the inhibition of 210K ß-glucosidase by D-glucono-1,5-lactone suggested the presence of 2 active sites similar to those of mammalian lactase-phlorizin hydrolase. Saccharification of sea lettuce was considerably stimulated by the synergistic action of 45K cellulase and 210K ß-glucosidase. Our results indicate that 45K cellulase and 210K ß-glucosidase are the core components of the sea hare digestive system for efficient production of glucose from sea lettuce. These findings contribute important new insights into the development of biofuel processing biotechnologies from seaweed.</description><subject>Agriculture</subject><subject>Algae</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>Analysis</subject><subject>Animals</subject><subject>Aplysia</subject><subject>Aplysia - enzymology</subject><subject>Aquatic microorganisms</subject><subject>Aquatic Organisms - enzymology</subject><subject>beta-Glucosidase - chemistry</subject><subject>beta-Glucosidase - isolation & purification</subject><subject>beta-Glucosidase - metabolism</subject><subject>Biodiesel fuels</subject><subject>Biofuels</subject><subject>Biology</subject><subject>Biomass</subject><subject>Biomass energy</subject><subject>Carboxymethyl cellulose</subject><subject>Carboxymethylcellulose</subject><subject>Cellobiose</subject><subject>Cellobiose - chemistry</subject><subject>Cellobiose - metabolism</subject><subject>Cellooligosaccharides</subject><subject>Cellulase</subject><subject>Cellulase - chemistry</subject><subject>Cellulase - isolation & purification</subject><subject>Cellulase - metabolism</subject><subject>Cellulose</subject><subject>Cellulose - analogs & derivatives</subject><subject>Cellulose - chemistry</subject><subject>Cellulose - metabolism</subject><subject>Cloning</subject><subject>Computational fluid dynamics</subject><subject>Digestive system</subject><subject>Endoglucanase</subject><subject>Engineering</subject><subject>Enzyme Assays</subject><subject>Enzymes</subject><subject>Ethanol</subject><subject>Evolution & development</subject><subject>Filter paper</subject><subject>Gastrointestinal Tract - enzymology</subject><subject>Glucans</subject><subject>Gluconates - chemistry</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Glucosidase</subject><subject>Glucosides - chemistry</subject><subject>Glucosides - metabolism</subject><subject>Hydrolase</subject><subject>Hydrolysis</subject><subject>Invertebrates</subject><subject>Kinetics</subject><subject>Lactase</subject><subject>Lactones - chemistry</subject><subject>Laminarin</subject><subject>Lettuce</subject><subject>Lignin</subject><subject>Lignocellulose</subject><subject>Molecular Sequence Data</subject><subject>Oligosaccharides</subject><subject>Polysaccharides</subject><subject>Polysaccharides - chemistry</subject><subject>Polysaccharides - metabolism</subject><subject>Proteins</subject><subject>Raw materials</subject><subject>Saccharides</subject><subject>Saccharification</subject><subject>Seaweeds</subject><subject>Substrate Specificity</subject><subject>Substrates</subject><subject>Tetroses - chemistry</subject><subject>Tetroses - metabolism</subject><subject>Trichoderma reesei</subject><subject>Ulva - chemistry</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk81u1DAQxyMEoqXwBggsISE47GLH-doLUlUKXalSJQpcLcceZ9068WInFcvL8DA8Ci_CZHdb7aIeUA52PL_5z4zHkyTPGZ0yXrJ3V34InXTTpe9gSmmRZ6x6kByyGU8nRUr5w539QfIkxitKc14VxePkIOVlkfKiOEz-nPh2GWABXbQ3QKD7uWplbxWRqL2KNhJvSL8AosC5wXm3Go1xFXtoie2Itg3EfnQ1brD6lr4ESc5kAHK8HFUkuR6C19JOyakxVlnoetK4QfkIJIADiasJviURHR30_aCA1CsM1EFobFxnpHrruzFClpPrDxKT1X4UwVTRXXaapIyuLb9_TTbqVqPpafLISBfh2XY9Sr5-PP1ycjY5v_g0Pzk-n6iSldVEskzLvE5LmFHFeV6UdZHpmQJlDMO_1GQl1RXjvOZpxTXMCpqWdZ1WDHeg-VHycqO7dD6KbX-iYLzIixz1ZkjMN4T28kosg21lWAkvrVgf-NAIGbBWB0IzBtjmujImyziTMtMc25ZxraihaYpa77fRhroFrfBKg3R7ovuWzi5E428EL8qc8QwF3mwFgv8-YBdFa-PYZtmBH9Z5lxWWSymir_5B769uSzUSC7Cd8RhXjaLiOCurjDGWl0hN76Hw09BahY_ZWDzfc3i754BMDz_6Rg4xivnl5_9nL77ts6932AVI1y-id8P4yuI-mG1AFXyMAczdJTMqxlm8vQ0xzqLYziK6vdht0J3T7fDxvzRXMk0</recordid><startdate>20130606</startdate><enddate>20130606</enddate><creator>Tsuji, Akihiko</creator><creator>Tominaga, Keiko</creator><creator>Nishiyama, Nami</creator><creator>Yuasa, Keizo</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130606</creationdate><title>Comprehensive enzymatic analysis of the cellulolytic system in digestive fluid of the Sea Hare Aplysia kurodai. Efficient glucose release from sea lettuce by synergistic action of 45 kDa endoglucanase and 210 kDa ß-glucosidase</title><author>Tsuji, Akihiko ; Tominaga, Keiko ; Nishiyama, Nami ; Yuasa, Keizo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c7178-a14da5b27e90c33567b64d9cecff15672f470d8133b3283de96027bb281960ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Agriculture</topic><topic>Algae</topic><topic>Amino Acid Sequence</topic><topic>Amino acids</topic><topic>Analysis</topic><topic>Animals</topic><topic>Aplysia</topic><topic>Aplysia - enzymology</topic><topic>Aquatic microorganisms</topic><topic>Aquatic Organisms - enzymology</topic><topic>beta-Glucosidase - chemistry</topic><topic>beta-Glucosidase - isolation & purification</topic><topic>beta-Glucosidase - metabolism</topic><topic>Biodiesel fuels</topic><topic>Biofuels</topic><topic>Biology</topic><topic>Biomass</topic><topic>Biomass energy</topic><topic>Carboxymethyl cellulose</topic><topic>Carboxymethylcellulose</topic><topic>Cellobiose</topic><topic>Cellobiose - 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chemistry</topic><topic>Laminarin</topic><topic>Lettuce</topic><topic>Lignin</topic><topic>Lignocellulose</topic><topic>Molecular Sequence Data</topic><topic>Oligosaccharides</topic><topic>Polysaccharides</topic><topic>Polysaccharides - chemistry</topic><topic>Polysaccharides - metabolism</topic><topic>Proteins</topic><topic>Raw materials</topic><topic>Saccharides</topic><topic>Saccharification</topic><topic>Seaweeds</topic><topic>Substrate Specificity</topic><topic>Substrates</topic><topic>Tetroses - chemistry</topic><topic>Tetroses - metabolism</topic><topic>Trichoderma reesei</topic><topic>Ulva - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsuji, Akihiko</creatorcontrib><creatorcontrib>Tominaga, Keiko</creatorcontrib><creatorcontrib>Nishiyama, Nami</creatorcontrib><creatorcontrib>Yuasa, Keizo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Opposing Viewpoints in Context (Gale)</collection><collection>Science (Gale in Context)</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>https://resources.nclive.org/materials</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsuji, Akihiko</au><au>Tominaga, Keiko</au><au>Nishiyama, Nami</au><au>Yuasa, Keizo</au><au>Sanchez-Ruiz, Jose M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comprehensive enzymatic analysis of the cellulolytic system in digestive fluid of the Sea Hare Aplysia kurodai. Efficient glucose release from sea lettuce by synergistic action of 45 kDa endoglucanase and 210 kDa ß-glucosidase</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-06-06</date><risdate>2013</risdate><volume>8</volume><issue>6</issue><spage>e65418</spage><epage>e65418</epage><pages>e65418-e65418</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Although many endo-ß-1,4-glucanases have been isolated in invertebrates, their cellulolytic systems are not fully understood. In particular, gastropod feeding on seaweed is considered an excellent model system for production of bioethanol and renewable bioenergy from third-generation feedstocks (microalgae and seaweeds). In this study, enzymes involved in the conversion of cellulose and other polysaccharides to glucose in digestive fluids of the sea hare (Aplysia kurodai) were screened and characterized to determine how the sea hare obtains glucose from sea lettuce (Ulva pertusa). Four endo-ß-1,4-glucanases (21K, 45K, 65K, and 95K cellulase) and 2 ß-glucosidases (110K and 210K) were purified to a homogeneous state, and the synergistic action of these enzymes during cellulose digestion was analyzed. All cellulases exhibited cellulase and lichenase activities and showed distinct cleavage specificities against cellooligosaccharides and filter paper. Filter paper was digested to cellobiose, cellotriose, and cellotetraose by 21K cellulase, whereas 45K and 65K enzymes hydrolyzed the filter paper to cellobiose and glucose. 210K ß-glucosidase showed unique substrate specificity against synthetic and natural substrates, and 4-methylumbelliferyl (4MU)-ß-glucoside, 4MU-ß-galactoside, cello-oligosaccharides, laminarin, and lichenan were suitable substrates. Furthermore, 210K ß-glucosidase possesses lactase activity. Although ß-glucosidase and cellulase are necessary for efficient hydrolysis of carboxymethylcellulose to glucose, laminarin is hydrolyzed to glucose only by 210K ß-glucosidase. Kinetic analysis of the inhibition of 210K ß-glucosidase by D-glucono-1,5-lactone suggested the presence of 2 active sites similar to those of mammalian lactase-phlorizin hydrolase. Saccharification of sea lettuce was considerably stimulated by the synergistic action of 45K cellulase and 210K ß-glucosidase. Our results indicate that 45K cellulase and 210K ß-glucosidase are the core components of the sea hare digestive system for efficient production of glucose from sea lettuce. These findings contribute important new insights into the development of biofuel processing biotechnologies from seaweed.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23762366</pmid><doi>10.1371/journal.pone.0065418</doi><tpages>e65418</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2013-06, Vol.8 (6), p.e65418-e65418 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1365653569 |
source | Publicly Available Content Database; PubMed Central |
subjects | Agriculture Algae Amino Acid Sequence Amino acids Analysis Animals Aplysia Aplysia - enzymology Aquatic microorganisms Aquatic Organisms - enzymology beta-Glucosidase - chemistry beta-Glucosidase - isolation & purification beta-Glucosidase - metabolism Biodiesel fuels Biofuels Biology Biomass Biomass energy Carboxymethyl cellulose Carboxymethylcellulose Cellobiose Cellobiose - chemistry Cellobiose - metabolism Cellooligosaccharides Cellulase Cellulase - chemistry Cellulase - isolation & purification Cellulase - metabolism Cellulose Cellulose - analogs & derivatives Cellulose - chemistry Cellulose - metabolism Cloning Computational fluid dynamics Digestive system Endoglucanase Engineering Enzyme Assays Enzymes Ethanol Evolution & development Filter paper Gastrointestinal Tract - enzymology Glucans Gluconates - chemistry Glucose Glucose - metabolism Glucosidase Glucosides - chemistry Glucosides - metabolism Hydrolase Hydrolysis Invertebrates Kinetics Lactase Lactones - chemistry Laminarin Lettuce Lignin Lignocellulose Molecular Sequence Data Oligosaccharides Polysaccharides Polysaccharides - chemistry Polysaccharides - metabolism Proteins Raw materials Saccharides Saccharification Seaweeds Substrate Specificity Substrates Tetroses - chemistry Tetroses - metabolism Trichoderma reesei Ulva - chemistry |
title | Comprehensive enzymatic analysis of the cellulolytic system in digestive fluid of the Sea Hare Aplysia kurodai. Efficient glucose release from sea lettuce by synergistic action of 45 kDa endoglucanase and 210 kDa ß-glucosidase |
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