Physiology of digestion and the molecular characterization of the major digestive enzymes from Periplaneta americana
[Display omitted] •The Periplaneta americana major digestive enzymes had their coding sequences cloned.•Electrophoretic and chromatographic data identified glucosidases, trypsins and chymotrypsins.•Enzyme distribution showed the relative importance of crop and posterior midgut in digestion.•A counte...
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•The Periplaneta americana major digestive enzymes had their coding sequences cloned.•Electrophoretic and chromatographic data identified glucosidases, trypsins and chymotrypsins.•Enzyme distribution showed the relative importance of crop and posterior midgut in digestion.•A countercurrent flux of fluid is functional in midgut in preventing enzyme excretion.•Enzyme secretion occurs by exocytic and apocrine mechanisms.
Cockroaches are among the first insects to appear in the fossil record. This work is part of ongoing research on insects at critical points in the evolutionary tree to disclose evolutionary trends in the digestive characteristics of insects. A transcriptome (454 Roche platform) of the midgut of Periplanetaamericana was searched for sequences of digestive enzymes. The selected sequences were manually curated. The complete or nearly complete sequences showing all characteristic motifs and highly expressed (reads counting) had their predicted sequences checked by cloning and Sanger sequencing. There are two chitinases (lacking mucin and chitin-binding domains), one amylase, two α- and three β-glucosidases, one β-galactosidase, two aminopeptidases (none of the N-group), one chymotrypsin, 5 trypsins, and none β-glucanase. Electrophoretic and enzymological data agreed with transcriptome data in showing that there is a single β-galactosidase, two α-glucosidases, one preferring as substrate maltase and the other aryl α-glucoside, and two β-glucosidases. Chromatographic and enzymological data identified 4 trypsins, one chymotrypsin (also found in the transcriptome), and one non-identified proteinase. The major digestive trypsin is identifiable to a major P. americana allergen (Per a 10). The lack of β-glucanase expression in midguts was confirmed, thus lending support to claims that those enzymes are salivary. A salivary amylase was molecularly cloned and shown to be different from the one from the midgut. Enzyme distribution showed that most digestion occurs under the action of salivary and midgut enzymes in the foregut and anterior midgut, except the posterior terminal digestion of proteins. A counter-flux of fluid may be functional in the midgut of the cockroach to explain the low excretory rate of digestive enzymes. Ultrastructural and immunocytochemical localization data showed that amylase and trypsin are released by both merocrine and apocrine secretion mainly from gastric caeca. Finally, a discussion on Polyneoptera digestive |
doi_str_mv | 10.1016/j.jinsphys.2014.08.007 |
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•The Periplaneta americana major digestive enzymes had their coding sequences cloned.•Electrophoretic and chromatographic data identified glucosidases, trypsins and chymotrypsins.•Enzyme distribution showed the relative importance of crop and posterior midgut in digestion.•A countercurrent flux of fluid is functional in midgut in preventing enzyme excretion.•Enzyme secretion occurs by exocytic and apocrine mechanisms.
Cockroaches are among the first insects to appear in the fossil record. This work is part of ongoing research on insects at critical points in the evolutionary tree to disclose evolutionary trends in the digestive characteristics of insects. A transcriptome (454 Roche platform) of the midgut of Periplanetaamericana was searched for sequences of digestive enzymes. The selected sequences were manually curated. The complete or nearly complete sequences showing all characteristic motifs and highly expressed (reads counting) had their predicted sequences checked by cloning and Sanger sequencing. There are two chitinases (lacking mucin and chitin-binding domains), one amylase, two α- and three β-glucosidases, one β-galactosidase, two aminopeptidases (none of the N-group), one chymotrypsin, 5 trypsins, and none β-glucanase. Electrophoretic and enzymological data agreed with transcriptome data in showing that there is a single β-galactosidase, two α-glucosidases, one preferring as substrate maltase and the other aryl α-glucoside, and two β-glucosidases. Chromatographic and enzymological data identified 4 trypsins, one chymotrypsin (also found in the transcriptome), and one non-identified proteinase. The major digestive trypsin is identifiable to a major P. americana allergen (Per a 10). The lack of β-glucanase expression in midguts was confirmed, thus lending support to claims that those enzymes are salivary. A salivary amylase was molecularly cloned and shown to be different from the one from the midgut. Enzyme distribution showed that most digestion occurs under the action of salivary and midgut enzymes in the foregut and anterior midgut, except the posterior terminal digestion of proteins. A counter-flux of fluid may be functional in the midgut of the cockroach to explain the low excretory rate of digestive enzymes. Ultrastructural and immunocytochemical localization data showed that amylase and trypsin are released by both merocrine and apocrine secretion mainly from gastric caeca. Finally, a discussion on Polyneoptera digestive physiology is provided.</description><identifier>ISSN: 0022-1910</identifier><identifier>EISSN: 1879-1611</identifier><identifier>DOI: 10.1016/j.jinsphys.2014.08.007</identifier><identifier>PMID: 25193546</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Aminopeptidases - genetics ; Aminopeptidases - physiology ; Animals ; Base Sequence ; beta-Galactosidase - genetics ; beta-Galactosidase - physiology ; beta-Glucosidase - genetics ; beta-Glucosidase - physiology ; Carbohydrases ; Chitinases - genetics ; Chitinases - physiology ; Chymotrypsin - genetics ; Chymotrypsin - physiology ; Digestion - physiology ; Digestive enzymes sequences ; Enzyme immunocytolocalization ; Gastrointestinal Tract - anatomy & histology ; Gastrointestinal Tract - diagnostic imaging ; Glucosidases - genetics ; Glucosidases - physiology ; Microscopy, Electron ; Molecular Sequence Data ; Peptide Hydrolases - genetics ; Peptide Hydrolases - physiology ; Periplaneta - anatomy & histology ; Periplaneta - enzymology ; Periplaneta - genetics ; Periplaneta - physiology ; Periplaneta americana ; Polymerase Chain Reaction ; Polyneoptera ; Proteases ; Secretory mechanism ; Transcriptome - genetics ; Trypsin - genetics ; Trypsin - physiology ; Ultrasonography</subject><ispartof>Journal of insect physiology, 2014-11, Vol.70, p.22-35</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-d14bb0105d2cb3ef35ba818a97ecad32d06069076f8640a734e256440cf1dbab3</citedby><cites>FETCH-LOGICAL-c467t-d14bb0105d2cb3ef35ba818a97ecad32d06069076f8640a734e256440cf1dbab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022191014001632$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25193546$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tamaki, Fábio K.</creatorcontrib><creatorcontrib>Pimentel, André C.</creatorcontrib><creatorcontrib>Dias, Alcides B.</creatorcontrib><creatorcontrib>Cardoso, Christiane</creatorcontrib><creatorcontrib>Ribeiro, Alberto F.</creatorcontrib><creatorcontrib>Ferreira, Clélia</creatorcontrib><creatorcontrib>Terra, Walter R.</creatorcontrib><title>Physiology of digestion and the molecular characterization of the major digestive enzymes from Periplaneta americana</title><title>Journal of insect physiology</title><addtitle>J Insect Physiol</addtitle><description>[Display omitted]
•The Periplaneta americana major digestive enzymes had their coding sequences cloned.•Electrophoretic and chromatographic data identified glucosidases, trypsins and chymotrypsins.•Enzyme distribution showed the relative importance of crop and posterior midgut in digestion.•A countercurrent flux of fluid is functional in midgut in preventing enzyme excretion.•Enzyme secretion occurs by exocytic and apocrine mechanisms.
Cockroaches are among the first insects to appear in the fossil record. This work is part of ongoing research on insects at critical points in the evolutionary tree to disclose evolutionary trends in the digestive characteristics of insects. A transcriptome (454 Roche platform) of the midgut of Periplanetaamericana was searched for sequences of digestive enzymes. The selected sequences were manually curated. The complete or nearly complete sequences showing all characteristic motifs and highly expressed (reads counting) had their predicted sequences checked by cloning and Sanger sequencing. There are two chitinases (lacking mucin and chitin-binding domains), one amylase, two α- and three β-glucosidases, one β-galactosidase, two aminopeptidases (none of the N-group), one chymotrypsin, 5 trypsins, and none β-glucanase. Electrophoretic and enzymological data agreed with transcriptome data in showing that there is a single β-galactosidase, two α-glucosidases, one preferring as substrate maltase and the other aryl α-glucoside, and two β-glucosidases. Chromatographic and enzymological data identified 4 trypsins, one chymotrypsin (also found in the transcriptome), and one non-identified proteinase. The major digestive trypsin is identifiable to a major P. americana allergen (Per a 10). The lack of β-glucanase expression in midguts was confirmed, thus lending support to claims that those enzymes are salivary. A salivary amylase was molecularly cloned and shown to be different from the one from the midgut. Enzyme distribution showed that most digestion occurs under the action of salivary and midgut enzymes in the foregut and anterior midgut, except the posterior terminal digestion of proteins. A counter-flux of fluid may be functional in the midgut of the cockroach to explain the low excretory rate of digestive enzymes. Ultrastructural and immunocytochemical localization data showed that amylase and trypsin are released by both merocrine and apocrine secretion mainly from gastric caeca. Finally, a discussion on Polyneoptera digestive physiology is provided.</description><subject>Aminopeptidases - genetics</subject><subject>Aminopeptidases - physiology</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>beta-Galactosidase - genetics</subject><subject>beta-Galactosidase - physiology</subject><subject>beta-Glucosidase - genetics</subject><subject>beta-Glucosidase - physiology</subject><subject>Carbohydrases</subject><subject>Chitinases - genetics</subject><subject>Chitinases - physiology</subject><subject>Chymotrypsin - genetics</subject><subject>Chymotrypsin - physiology</subject><subject>Digestion - physiology</subject><subject>Digestive enzymes sequences</subject><subject>Enzyme immunocytolocalization</subject><subject>Gastrointestinal Tract - anatomy & histology</subject><subject>Gastrointestinal Tract - diagnostic imaging</subject><subject>Glucosidases - genetics</subject><subject>Glucosidases - physiology</subject><subject>Microscopy, Electron</subject><subject>Molecular Sequence Data</subject><subject>Peptide Hydrolases - genetics</subject><subject>Peptide Hydrolases - physiology</subject><subject>Periplaneta - anatomy & histology</subject><subject>Periplaneta - enzymology</subject><subject>Periplaneta - genetics</subject><subject>Periplaneta - physiology</subject><subject>Periplaneta americana</subject><subject>Polymerase Chain Reaction</subject><subject>Polyneoptera</subject><subject>Proteases</subject><subject>Secretory mechanism</subject><subject>Transcriptome - genetics</subject><subject>Trypsin - genetics</subject><subject>Trypsin - physiology</subject><subject>Ultrasonography</subject><issn>0022-1910</issn><issn>1879-1611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhi0EokvhL1Q-ckk6kw8nuYEqPipVogc4WxN70nWUxIudrbT99Xi7Xa5wGo30vDOjeYS4QsgRUF2P-eiWuNseYl4AVjm0OUDzSmywbboMFeJrsQEoigw7hAvxLsYRAGrV1m_FRVFjV9aV2oj1Po1wfvIPB-kHad0Dx9X5RdJi5bplOfuJzX6iIM2WApmVg3uiZyTxzwSNPpyTjyx5eTrMHOUQ_CzvE76baOGVJM2pMbTQe_FmoCnyh5d6KX59_fLz5nt29-Pb7c3nu8xUqlkzi1XfA0JtC9OXPJR1Ty221DVsyJaFBQWqg0YNraqAmrLiolZVBWZA21NfXoqPp7m74H_v03l6dtHwdLzH76NGVTUApUL1H2jRdY1SUCdUnVATfIyBB70LbqZw0Aj6KEeP-ixHH-VoaHWSk4JXLzv2_cz2b-xsIwGfTgCnpzw6Djoax4th6wKbVVvv_rXjDwcEpl0</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>Tamaki, Fábio K.</creator><creator>Pimentel, André C.</creator><creator>Dias, Alcides B.</creator><creator>Cardoso, Christiane</creator><creator>Ribeiro, Alberto F.</creator><creator>Ferreira, Clélia</creator><creator>Terra, Walter R.</creator><general>Elsevier 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>7X8</scope><scope>7SS</scope></search><sort><creationdate>20141101</creationdate><title>Physiology of digestion and the molecular characterization of the major digestive enzymes from Periplaneta americana</title><author>Tamaki, Fábio K. ; Pimentel, André C. ; Dias, Alcides B. ; Cardoso, Christiane ; Ribeiro, Alberto F. ; Ferreira, Clélia ; Terra, Walter R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-d14bb0105d2cb3ef35ba818a97ecad32d06069076f8640a734e256440cf1dbab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aminopeptidases - genetics</topic><topic>Aminopeptidases - physiology</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>beta-Galactosidase - genetics</topic><topic>beta-Galactosidase - physiology</topic><topic>beta-Glucosidase - genetics</topic><topic>beta-Glucosidase - physiology</topic><topic>Carbohydrases</topic><topic>Chitinases - genetics</topic><topic>Chitinases - physiology</topic><topic>Chymotrypsin - genetics</topic><topic>Chymotrypsin - physiology</topic><topic>Digestion - physiology</topic><topic>Digestive enzymes sequences</topic><topic>Enzyme immunocytolocalization</topic><topic>Gastrointestinal Tract - anatomy & histology</topic><topic>Gastrointestinal Tract - diagnostic imaging</topic><topic>Glucosidases - genetics</topic><topic>Glucosidases - physiology</topic><topic>Microscopy, Electron</topic><topic>Molecular Sequence Data</topic><topic>Peptide Hydrolases - genetics</topic><topic>Peptide Hydrolases - physiology</topic><topic>Periplaneta - anatomy & histology</topic><topic>Periplaneta - enzymology</topic><topic>Periplaneta - genetics</topic><topic>Periplaneta - physiology</topic><topic>Periplaneta americana</topic><topic>Polymerase Chain Reaction</topic><topic>Polyneoptera</topic><topic>Proteases</topic><topic>Secretory mechanism</topic><topic>Transcriptome - genetics</topic><topic>Trypsin - genetics</topic><topic>Trypsin - physiology</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamaki, Fábio K.</creatorcontrib><creatorcontrib>Pimentel, André C.</creatorcontrib><creatorcontrib>Dias, Alcides B.</creatorcontrib><creatorcontrib>Cardoso, Christiane</creatorcontrib><creatorcontrib>Ribeiro, Alberto F.</creatorcontrib><creatorcontrib>Ferreira, Clélia</creatorcontrib><creatorcontrib>Terra, Walter R.</creatorcontrib><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>Entomology Abstracts (Full archive)</collection><jtitle>Journal of insect physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamaki, Fábio K.</au><au>Pimentel, André C.</au><au>Dias, Alcides B.</au><au>Cardoso, Christiane</au><au>Ribeiro, Alberto F.</au><au>Ferreira, Clélia</au><au>Terra, Walter R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physiology of digestion and the molecular characterization of the major digestive enzymes from Periplaneta americana</atitle><jtitle>Journal of insect physiology</jtitle><addtitle>J Insect Physiol</addtitle><date>2014-11-01</date><risdate>2014</risdate><volume>70</volume><spage>22</spage><epage>35</epage><pages>22-35</pages><issn>0022-1910</issn><eissn>1879-1611</eissn><abstract>[Display omitted]
•The Periplaneta americana major digestive enzymes had their coding sequences cloned.•Electrophoretic and chromatographic data identified glucosidases, trypsins and chymotrypsins.•Enzyme distribution showed the relative importance of crop and posterior midgut in digestion.•A countercurrent flux of fluid is functional in midgut in preventing enzyme excretion.•Enzyme secretion occurs by exocytic and apocrine mechanisms.
Cockroaches are among the first insects to appear in the fossil record. This work is part of ongoing research on insects at critical points in the evolutionary tree to disclose evolutionary trends in the digestive characteristics of insects. A transcriptome (454 Roche platform) of the midgut of Periplanetaamericana was searched for sequences of digestive enzymes. The selected sequences were manually curated. The complete or nearly complete sequences showing all characteristic motifs and highly expressed (reads counting) had their predicted sequences checked by cloning and Sanger sequencing. There are two chitinases (lacking mucin and chitin-binding domains), one amylase, two α- and three β-glucosidases, one β-galactosidase, two aminopeptidases (none of the N-group), one chymotrypsin, 5 trypsins, and none β-glucanase. Electrophoretic and enzymological data agreed with transcriptome data in showing that there is a single β-galactosidase, two α-glucosidases, one preferring as substrate maltase and the other aryl α-glucoside, and two β-glucosidases. Chromatographic and enzymological data identified 4 trypsins, one chymotrypsin (also found in the transcriptome), and one non-identified proteinase. The major digestive trypsin is identifiable to a major P. americana allergen (Per a 10). The lack of β-glucanase expression in midguts was confirmed, thus lending support to claims that those enzymes are salivary. A salivary amylase was molecularly cloned and shown to be different from the one from the midgut. Enzyme distribution showed that most digestion occurs under the action of salivary and midgut enzymes in the foregut and anterior midgut, except the posterior terminal digestion of proteins. A counter-flux of fluid may be functional in the midgut of the cockroach to explain the low excretory rate of digestive enzymes. Ultrastructural and immunocytochemical localization data showed that amylase and trypsin are released by both merocrine and apocrine secretion mainly from gastric caeca. Finally, a discussion on Polyneoptera digestive physiology is provided.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25193546</pmid><doi>10.1016/j.jinsphys.2014.08.007</doi><tpages>14</tpages></addata></record> |
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subjects | Aminopeptidases - genetics Aminopeptidases - physiology Animals Base Sequence beta-Galactosidase - genetics beta-Galactosidase - physiology beta-Glucosidase - genetics beta-Glucosidase - physiology Carbohydrases Chitinases - genetics Chitinases - physiology Chymotrypsin - genetics Chymotrypsin - physiology Digestion - physiology Digestive enzymes sequences Enzyme immunocytolocalization Gastrointestinal Tract - anatomy & histology Gastrointestinal Tract - diagnostic imaging Glucosidases - genetics Glucosidases - physiology Microscopy, Electron Molecular Sequence Data Peptide Hydrolases - genetics Peptide Hydrolases - physiology Periplaneta - anatomy & histology Periplaneta - enzymology Periplaneta - genetics Periplaneta - physiology Periplaneta americana Polymerase Chain Reaction Polyneoptera Proteases Secretory mechanism Transcriptome - genetics Trypsin - genetics Trypsin - physiology Ultrasonography |
title | Physiology of digestion and the molecular characterization of the major digestive enzymes from Periplaneta americana |
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