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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Veröffentlicht in:Journal of insect physiology 2014-11, Vol.70, p.22-35
Hauptverfasser: Tamaki, Fábio K., Pimentel, André C., Dias, Alcides B., Cardoso, Christiane, Ribeiro, Alberto F., Ferreira, Clélia, Terra, Walter R.
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container_issue
container_start_page 22
container_title Journal of insect physiology
container_volume 70
creator Tamaki, Fábio K.
Pimentel, André C.
Dias, Alcides B.
Cardoso, Christiane
Ribeiro, Alberto F.
Ferreira, Clélia
Terra, Walter R.
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
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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 &amp; histology ; Gastrointestinal Tract - diagnostic imaging ; Glucosidases - genetics ; Glucosidases - physiology ; Microscopy, Electron ; Molecular Sequence Data ; Peptide Hydrolases - genetics ; Peptide Hydrolases - physiology ; Periplaneta - anatomy &amp; 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. 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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. ; 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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 &amp; 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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