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Identification and in-silico characterization of taxadien-5α-ol-O-acetyltransferase (TDAT) gene in Corylus avellana L
Paclitaxel® (PC) is one of the most effective and profitable anti-cancer drugs. The most promising sources of this compound are natural materials such as tissue cultures of Taxus species and, more recently, hazelnut (Corylus avellana L.). A large part of the PC biosynthetic pathway in the yew tree a...
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Published in: | PloS one 2021-08, Vol.16 (8), p.e0256704-e0256704 |
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description | Paclitaxel® (PC) is one of the most effective and profitable anti-cancer drugs. The most promising sources of this compound are natural materials such as tissue cultures of Taxus species and, more recently, hazelnut (Corylus avellana L.). A large part of the PC biosynthetic pathway in the yew tree and a few steps in the hazelnut have been identified. Since understanding the biosynthetic pathway of plant-based medicinal metabolites is an effective step toward their development and engineering, this paper aimed to identify taxadiene-5α-ol-O-acetyltransferase (TDAT) in hazelnut. TDAT is one of the key genes involved in the third step of the PC biosynthetic pathway. In this study, the TDAT gene was isolated using the nested-PCR method and then characterized. The cotyledon-derived cell mass induced with 150 μM of methyl jasmonate (MeJA) was utilized to isolate RNA and synthesize the first-strand cDNA. The full-length cDNA of TDAT is 1423 bp long and contains a 1302 bp ORF encoding 433 amino acids. The phylogenetic analysis of this gene revealed high homology with its ortholog genes in Quercus suber and Juglans regia. Bioinformatics analyses were used to predict the secondary and tertiary structures of the protein. Due to the lack of signal peptide, protein structure prediction suggested that this protein may operate at the cytoplasm. The homologous superfamily of the T5AT protein, encoded by TDAT, has two domains. The highest and lowest hydrophobicity of amino acids were found in proline 142 and lysine 56, respectively. T5AT protein fragment had 24 hydrophobic regions. The tertiary structure of this protein was designed using Modeler software (V.9.20), and its structure was verified based on the results of the Verify3D (89.46%) and ERRAT (90.3061) programs. The T5AT enzyme belongs to the superfamily of the transferase, and the amino acids histidine 164, cysteine 165, leucine 166, histidine 167, and Aspartic acid 168 resided at its active site. More characteristics of TDAT, which would aid PC engineering programs and maximize its production in hazelnut, were discussed. |
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The most promising sources of this compound are natural materials such as tissue cultures of Taxus species and, more recently, hazelnut (Corylus avellana L.). A large part of the PC biosynthetic pathway in the yew tree and a few steps in the hazelnut have been identified. Since understanding the biosynthetic pathway of plant-based medicinal metabolites is an effective step toward their development and engineering, this paper aimed to identify taxadiene-5α-ol-O-acetyltransferase (TDAT) in hazelnut. TDAT is one of the key genes involved in the third step of the PC biosynthetic pathway. In this study, the TDAT gene was isolated using the nested-PCR method and then characterized. The cotyledon-derived cell mass induced with 150 μM of methyl jasmonate (MeJA) was utilized to isolate RNA and synthesize the first-strand cDNA. The full-length cDNA of TDAT is 1423 bp long and contains a 1302 bp ORF encoding 433 amino acids. The phylogenetic analysis of this gene revealed high homology with its ortholog genes in Quercus suber and Juglans regia. Bioinformatics analyses were used to predict the secondary and tertiary structures of the protein. Due to the lack of signal peptide, protein structure prediction suggested that this protein may operate at the cytoplasm. The homologous superfamily of the T5AT protein, encoded by TDAT, has two domains. The highest and lowest hydrophobicity of amino acids were found in proline 142 and lysine 56, respectively. T5AT protein fragment had 24 hydrophobic regions. The tertiary structure of this protein was designed using Modeler software (V.9.20), and its structure was verified based on the results of the Verify3D (89.46%) and ERRAT (90.3061) programs. The T5AT enzyme belongs to the superfamily of the transferase, and the amino acids histidine 164, cysteine 165, leucine 166, histidine 167, and Aspartic acid 168 resided at its active site. More characteristics of TDAT, which would aid PC engineering programs and maximize its production in hazelnut, were discussed.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0256704</identifier><identifier>PMID: 34449796</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acetyltransferase ; Acetyltransferases - chemistry ; Acetyltransferases - genetics ; Acetyltransferases - therapeutic use ; Agricultural biotechnology ; Amino Acid Sequence - genetics ; Amino acids ; Anticancer properties ; Antitumor agents ; Aspartic acid ; Bioinformatics ; Biological Products - chemistry ; Biology and Life Sciences ; Biosynthesis ; Cancer ; Cell culture ; Cell cycle ; Computer and Information Sciences ; Computer programs ; Corylus - chemistry ; Corylus avellana ; Cytoplasm ; Engineering ; Engineering and Technology ; Enzymes ; Ethanol ; Gene banks ; Genes ; Hazelnuts ; Histidine ; Homology ; Humans ; Hydrophobicity ; Jasmonic acid ; Leucine ; Lysine ; Medicinal plants ; Metabolism ; Metabolites ; Methyl jasmonate ; Neoplasms - drug therapy ; Open reading frames ; Paclitaxel ; Paclitaxel - chemistry ; Paclitaxel - therapeutic use ; Phylogeny ; Plants, Medicinal - chemistry ; Proline ; Protein structure ; Proteins ; Research and Analysis Methods ; Seeds ; Taxus - chemistry ; Tertiary structure</subject><ispartof>PloS one, 2021-08, Vol.16 (8), p.e0256704-e0256704</ispartof><rights>2021 Raeispour Shirazi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://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>2021 Raeispour Shirazi et al 2021 Raeispour Shirazi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-cb07bd94a584a89009ae16a90d404c10a529f6a2316c2a9c7936b9e9cdc1bdbf3</citedby><cites>FETCH-LOGICAL-c526t-cb07bd94a584a89009ae16a90d404c10a529f6a2316c2a9c7936b9e9cdc1bdbf3</cites><orcidid>0000-0001-5518-3703</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2565449241/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2565449241?pq-origsite=primo$$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/34449796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Srinivasan, Balamurugan</contributor><creatorcontrib>Raeispour Shirazi, Mona</creatorcontrib><creatorcontrib>Rahpeyma, Sara Alsadat</creatorcontrib><creatorcontrib>Rashidi Monfared, Sajad</creatorcontrib><creatorcontrib>Zolala, Jafar</creatorcontrib><creatorcontrib>Lohrasbi-Nejad, Azadeh</creatorcontrib><title>Identification and in-silico characterization of taxadien-5α-ol-O-acetyltransferase (TDAT) gene in Corylus avellana L</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Paclitaxel® (PC) is one of the most effective and profitable anti-cancer drugs. The most promising sources of this compound are natural materials such as tissue cultures of Taxus species and, more recently, hazelnut (Corylus avellana L.). A large part of the PC biosynthetic pathway in the yew tree and a few steps in the hazelnut have been identified. Since understanding the biosynthetic pathway of plant-based medicinal metabolites is an effective step toward their development and engineering, this paper aimed to identify taxadiene-5α-ol-O-acetyltransferase (TDAT) in hazelnut. TDAT is one of the key genes involved in the third step of the PC biosynthetic pathway. In this study, the TDAT gene was isolated using the nested-PCR method and then characterized. The cotyledon-derived cell mass induced with 150 μM of methyl jasmonate (MeJA) was utilized to isolate RNA and synthesize the first-strand cDNA. The full-length cDNA of TDAT is 1423 bp long and contains a 1302 bp ORF encoding 433 amino acids. The phylogenetic analysis of this gene revealed high homology with its ortholog genes in Quercus suber and Juglans regia. Bioinformatics analyses were used to predict the secondary and tertiary structures of the protein. Due to the lack of signal peptide, protein structure prediction suggested that this protein may operate at the cytoplasm. The homologous superfamily of the T5AT protein, encoded by TDAT, has two domains. The highest and lowest hydrophobicity of amino acids were found in proline 142 and lysine 56, respectively. T5AT protein fragment had 24 hydrophobic regions. The tertiary structure of this protein was designed using Modeler software (V.9.20), and its structure was verified based on the results of the Verify3D (89.46%) and ERRAT (90.3061) programs. The T5AT enzyme belongs to the superfamily of the transferase, and the amino acids histidine 164, cysteine 165, leucine 166, histidine 167, and Aspartic acid 168 resided at its active site. More characteristics of TDAT, which would aid PC engineering programs and maximize its production in hazelnut, were discussed.</description><subject>Acetyltransferase</subject><subject>Acetyltransferases - chemistry</subject><subject>Acetyltransferases - genetics</subject><subject>Acetyltransferases - therapeutic use</subject><subject>Agricultural biotechnology</subject><subject>Amino Acid Sequence - genetics</subject><subject>Amino acids</subject><subject>Anticancer properties</subject><subject>Antitumor agents</subject><subject>Aspartic acid</subject><subject>Bioinformatics</subject><subject>Biological Products - chemistry</subject><subject>Biology and Life Sciences</subject><subject>Biosynthesis</subject><subject>Cancer</subject><subject>Cell culture</subject><subject>Cell cycle</subject><subject>Computer and Information Sciences</subject><subject>Computer programs</subject><subject>Corylus - chemistry</subject><subject>Corylus avellana</subject><subject>Cytoplasm</subject><subject>Engineering</subject><subject>Engineering and Technology</subject><subject>Enzymes</subject><subject>Ethanol</subject><subject>Gene banks</subject><subject>Genes</subject><subject>Hazelnuts</subject><subject>Histidine</subject><subject>Homology</subject><subject>Humans</subject><subject>Hydrophobicity</subject><subject>Jasmonic acid</subject><subject>Leucine</subject><subject>Lysine</subject><subject>Medicinal plants</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Methyl jasmonate</subject><subject>Neoplasms - drug therapy</subject><subject>Open reading frames</subject><subject>Paclitaxel</subject><subject>Paclitaxel - chemistry</subject><subject>Paclitaxel - therapeutic use</subject><subject>Phylogeny</subject><subject>Plants, Medicinal - chemistry</subject><subject>Proline</subject><subject>Protein structure</subject><subject>Proteins</subject><subject>Research and Analysis Methods</subject><subject>Seeds</subject><subject>Taxus - chemistry</subject><subject>Tertiary structure</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkstuEzEUhkcIREvhDRCMxKYsJvg2nvEGqQq3SJG6CWvr-DKpI8cO9kxEeCtehGdimkyrFrGy5fOfz-f8-oviNUYzTBv8YROHFMDPdjHYGSI1bxB7UpxjQUnFCaJPH9zPihc5bxCqacv58-KMMsZEI_h5sV8YG3rXOQ29i6GEYEoXquy807HUN5BA9za5X6dy7MoefoJxNlT1n99V9NV1Bdr2B98nCLmzCbItL1efrlbvy7UNdqSV85gOfsgl7K33EKBcviyedeCzfTWdF8X3L59X82_V8vrrYn61rHRNeF9phRplBIO6ZdAKhARYzEEgwxDTGEFNRMeBUMw1AaEbQbkSVmijsTKqoxfF2xN352OWk2VZjm7VowOE4VGxOClMhI3cJbeFdJARnDw-xLSWkHqnvZVIIc20UljxhnGhFDFdzXTTtla0mJOR9XH6bVBba_TobAL_CPq4EtyNXMe9bKngDW5GwOUESPHHYHMvty7ro2k2Dse5OaICEzpK3_0j_f927KTSKeacbHc_DEbyNkZ3XfI2RnKK0dj25uEi9013uaF_AYhXx8M</recordid><startdate>20210827</startdate><enddate>20210827</enddate><creator>Raeispour Shirazi, Mona</creator><creator>Rahpeyma, Sara Alsadat</creator><creator>Rashidi Monfared, Sajad</creator><creator>Zolala, Jafar</creator><creator>Lohrasbi-Nejad, Azadeh</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>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>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5518-3703</orcidid></search><sort><creationdate>20210827</creationdate><title>Identification and in-silico characterization of taxadien-5α-ol-O-acetyltransferase (TDAT) gene in Corylus avellana L</title><author>Raeispour Shirazi, Mona ; Rahpeyma, Sara Alsadat ; Rashidi Monfared, Sajad ; Zolala, Jafar ; Lohrasbi-Nejad, Azadeh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-cb07bd94a584a89009ae16a90d404c10a529f6a2316c2a9c7936b9e9cdc1bdbf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acetyltransferase</topic><topic>Acetyltransferases - chemistry</topic><topic>Acetyltransferases - genetics</topic><topic>Acetyltransferases - therapeutic use</topic><topic>Agricultural biotechnology</topic><topic>Amino Acid Sequence - genetics</topic><topic>Amino acids</topic><topic>Anticancer properties</topic><topic>Antitumor agents</topic><topic>Aspartic acid</topic><topic>Bioinformatics</topic><topic>Biological Products - chemistry</topic><topic>Biology and Life Sciences</topic><topic>Biosynthesis</topic><topic>Cancer</topic><topic>Cell culture</topic><topic>Cell cycle</topic><topic>Computer and Information Sciences</topic><topic>Computer programs</topic><topic>Corylus - chemistry</topic><topic>Corylus avellana</topic><topic>Cytoplasm</topic><topic>Engineering</topic><topic>Engineering and Technology</topic><topic>Enzymes</topic><topic>Ethanol</topic><topic>Gene banks</topic><topic>Genes</topic><topic>Hazelnuts</topic><topic>Histidine</topic><topic>Homology</topic><topic>Humans</topic><topic>Hydrophobicity</topic><topic>Jasmonic acid</topic><topic>Leucine</topic><topic>Lysine</topic><topic>Medicinal plants</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Methyl jasmonate</topic><topic>Neoplasms - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raeispour Shirazi, Mona</au><au>Rahpeyma, Sara Alsadat</au><au>Rashidi Monfared, Sajad</au><au>Zolala, Jafar</au><au>Lohrasbi-Nejad, Azadeh</au><au>Srinivasan, Balamurugan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and in-silico characterization of taxadien-5α-ol-O-acetyltransferase (TDAT) gene in Corylus avellana L</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2021-08-27</date><risdate>2021</risdate><volume>16</volume><issue>8</issue><spage>e0256704</spage><epage>e0256704</epage><pages>e0256704-e0256704</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Paclitaxel® (PC) is one of the most effective and profitable anti-cancer drugs. The most promising sources of this compound are natural materials such as tissue cultures of Taxus species and, more recently, hazelnut (Corylus avellana L.). A large part of the PC biosynthetic pathway in the yew tree and a few steps in the hazelnut have been identified. Since understanding the biosynthetic pathway of plant-based medicinal metabolites is an effective step toward their development and engineering, this paper aimed to identify taxadiene-5α-ol-O-acetyltransferase (TDAT) in hazelnut. TDAT is one of the key genes involved in the third step of the PC biosynthetic pathway. In this study, the TDAT gene was isolated using the nested-PCR method and then characterized. The cotyledon-derived cell mass induced with 150 μM of methyl jasmonate (MeJA) was utilized to isolate RNA and synthesize the first-strand cDNA. The full-length cDNA of TDAT is 1423 bp long and contains a 1302 bp ORF encoding 433 amino acids. The phylogenetic analysis of this gene revealed high homology with its ortholog genes in Quercus suber and Juglans regia. Bioinformatics analyses were used to predict the secondary and tertiary structures of the protein. Due to the lack of signal peptide, protein structure prediction suggested that this protein may operate at the cytoplasm. The homologous superfamily of the T5AT protein, encoded by TDAT, has two domains. The highest and lowest hydrophobicity of amino acids were found in proline 142 and lysine 56, respectively. T5AT protein fragment had 24 hydrophobic regions. The tertiary structure of this protein was designed using Modeler software (V.9.20), and its structure was verified based on the results of the Verify3D (89.46%) and ERRAT (90.3061) programs. The T5AT enzyme belongs to the superfamily of the transferase, and the amino acids histidine 164, cysteine 165, leucine 166, histidine 167, and Aspartic acid 168 resided at its active site. More characteristics of TDAT, which would aid PC engineering programs and maximize its production in hazelnut, were discussed.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>34449796</pmid><doi>10.1371/journal.pone.0256704</doi><orcidid>https://orcid.org/0000-0001-5518-3703</orcidid><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2021-08, Vol.16 (8), p.e0256704-e0256704 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2565449241 |
source | Publicly Available Content (ProQuest); PubMed Central |
subjects | Acetyltransferase Acetyltransferases - chemistry Acetyltransferases - genetics Acetyltransferases - therapeutic use Agricultural biotechnology Amino Acid Sequence - genetics Amino acids Anticancer properties Antitumor agents Aspartic acid Bioinformatics Biological Products - chemistry Biology and Life Sciences Biosynthesis Cancer Cell culture Cell cycle Computer and Information Sciences Computer programs Corylus - chemistry Corylus avellana Cytoplasm Engineering Engineering and Technology Enzymes Ethanol Gene banks Genes Hazelnuts Histidine Homology Humans Hydrophobicity Jasmonic acid Leucine Lysine Medicinal plants Metabolism Metabolites Methyl jasmonate Neoplasms - drug therapy Open reading frames Paclitaxel Paclitaxel - chemistry Paclitaxel - therapeutic use Phylogeny Plants, Medicinal - chemistry Proline Protein structure Proteins Research and Analysis Methods Seeds Taxus - chemistry Tertiary structure |
title | Identification and in-silico characterization of taxadien-5α-ol-O-acetyltransferase (TDAT) gene in Corylus avellana L |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T20%3A27%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Identification%20and%20in-silico%20characterization%20of%20taxadien-5%CE%B1-ol-O-acetyltransferase%20(TDAT)%20gene%20in%20Corylus%20avellana%20L&rft.jtitle=PloS%20one&rft.au=Raeispour%20Shirazi,%20Mona&rft.date=2021-08-27&rft.volume=16&rft.issue=8&rft.spage=e0256704&rft.epage=e0256704&rft.pages=e0256704-e0256704&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0256704&rft_dat=%3Cproquest_plos_%3E2566039123%3C/proquest_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c526t-cb07bd94a584a89009ae16a90d404c10a529f6a2316c2a9c7936b9e9cdc1bdbf3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2565449241&rft_id=info:pmid/34449796&rfr_iscdi=true |