弗氏柠檬酸菌甘油脱水酶基因在大肠杆菌中的克隆和表达
以弗氏柠檬酸菌(Citrobacter freundii)基因组DNA为模板,通过PCR得到甘油脱水酶(glycerol dehydratase)基因dhaB、dhaC、dhaE,克隆到表达载体pSE380上,得到重组质粒pSn-dhaBCE。将此重组质粒转化到E.coli JM109中,重组菌株SDS-PAGE结果显示有明显的61kD、22kD、16kD三条特异性蛋白条带出现。重组菌株经诱导表达,酶活力为11.59U/mL。...
Gespeichert in:
Veröffentlicht in: | Gongye weishengwu 2005, Vol.35 (3), p.10-13 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | chi |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 13 |
---|---|
container_issue | 3 |
container_start_page | 10 |
container_title | Gongye weishengwu |
container_volume | 35 |
creator | 齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波 |
description | 以弗氏柠檬酸菌(Citrobacter freundii)基因组DNA为模板,通过PCR得到甘油脱水酶(glycerol dehydratase)基因dhaB、dhaC、dhaE,克隆到表达载体pSE380上,得到重组质粒pSn-dhaBCE。将此重组质粒转化到E.coli JM109中,重组菌株SDS-PAGE结果显示有明显的61kD、22kD、16kD三条特异性蛋白条带出现。重组菌株经诱导表达,酶活力为11.59U/mL。 |
doi_str_mv | 10.3969/j.issn.1001-6678.2005.03.003 |
format | Article |
fullrecord | <record><control><sourceid>wanfang_jour_chong</sourceid><recordid>TN_cdi_wanfang_journals_gywsw200503003</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>20186471</cqvip_id><wanfj_id>gywsw200503003</wanfj_id><sourcerecordid>gywsw200503003</sourcerecordid><originalsourceid>FETCH-LOGICAL-c583-5b633182331cec063c20d59b918b246a35618366117000672c91692147ac5f383</originalsourceid><addsrcrecordid>eNo9j89LAkEcxedQkFn_RES33b4zszM7cwzpFwldvMvu5JomK7WEdA31kiBEUFihQZBEgUWERfjXNOv6XzRhdHkPHh_e4yG0jMGmksvVsl2KotDGANji3BU2AWA2UBuAzqDUfz6H5qOobELpOCyFdvTXZTxox91e_Pg0aQyTdmt8cRW_fiT1l3jwNmm86-6nvu7pm76-f0hOe_Ft0zDfw-dxp64bZ5NOU5-3krt-MhotoNnAq0SFxT9Po9zGei6zZWV3N7cza1lLMUEt5nNKsSBGVEEBp4rAHpO-xMInDvco41hQzjF2AYC7REnMJcGO6ykWUEHTaGVaW_PCwAuL-XL1-Cg0g_niSS2q_f4Gag4acGkKqv1qWDwsGdT31EFQqhTyBLDgjovpD49FdDY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>弗氏柠檬酸菌甘油脱水酶基因在大肠杆菌中的克隆和表达</title><source>Alma/SFX Local Collection</source><creator>齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波</creator><creatorcontrib>齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波</creatorcontrib><description>以弗氏柠檬酸菌(Citrobacter freundii)基因组DNA为模板,通过PCR得到甘油脱水酶(glycerol dehydratase)基因dhaB、dhaC、dhaE,克隆到表达载体pSE380上,得到重组质粒pSn-dhaBCE。将此重组质粒转化到E.coli JM109中,重组菌株SDS-PAGE结果显示有明显的61kD、22kD、16kD三条特异性蛋白条带出现。重组菌株经诱导表达,酶活力为11.59U/mL。</description><identifier>ISSN: 1001-6678</identifier><identifier>DOI: 10.3969/j.issn.1001-6678.2005.03.003</identifier><language>chi</language><publisher>广西大学广西亚热带生物资源保护利用重点实验室,南宁,530005%南宁中诺生物工程有限公司,南宁,530005</publisher><subject>SDS-PAGE ; 克隆 ; 克隆和表达 ; 基因组DNA ; 大肠杆菌 ; 弗氏柠檬酸菌 ; 柠檬酸 ; 甘油脱水酶 ; 表达 ; 酶基因</subject><ispartof>Gongye weishengwu, 2005, Vol.35 (3), p.10-13</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/92972X/92972X.jpg</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids></links><search><creatorcontrib>齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波</creatorcontrib><title>弗氏柠檬酸菌甘油脱水酶基因在大肠杆菌中的克隆和表达</title><title>Gongye weishengwu</title><addtitle>Industrial Microbiology</addtitle><description>以弗氏柠檬酸菌(Citrobacter freundii)基因组DNA为模板,通过PCR得到甘油脱水酶(glycerol dehydratase)基因dhaB、dhaC、dhaE,克隆到表达载体pSE380上,得到重组质粒pSn-dhaBCE。将此重组质粒转化到E.coli JM109中,重组菌株SDS-PAGE结果显示有明显的61kD、22kD、16kD三条特异性蛋白条带出现。重组菌株经诱导表达,酶活力为11.59U/mL。</description><subject>SDS-PAGE</subject><subject>克隆</subject><subject>克隆和表达</subject><subject>基因组DNA</subject><subject>大肠杆菌</subject><subject>弗氏柠檬酸菌</subject><subject>柠檬酸</subject><subject>甘油脱水酶</subject><subject>表达</subject><subject>酶基因</subject><issn>1001-6678</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNo9j89LAkEcxedQkFn_RES33b4zszM7cwzpFwldvMvu5JomK7WEdA31kiBEUFihQZBEgUWERfjXNOv6XzRhdHkPHh_e4yG0jMGmksvVsl2KotDGANji3BU2AWA2UBuAzqDUfz6H5qOobELpOCyFdvTXZTxox91e_Pg0aQyTdmt8cRW_fiT1l3jwNmm86-6nvu7pm76-f0hOe_Ft0zDfw-dxp64bZ5NOU5-3krt-MhotoNnAq0SFxT9Po9zGei6zZWV3N7cza1lLMUEt5nNKsSBGVEEBp4rAHpO-xMInDvco41hQzjF2AYC7REnMJcGO6ykWUEHTaGVaW_PCwAuL-XL1-Cg0g_niSS2q_f4Gag4acGkKqv1qWDwsGdT31EFQqhTyBLDgjovpD49FdDY</recordid><startdate>2005</startdate><enddate>2005</enddate><creator>齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波</creator><general>广西大学广西亚热带生物资源保护利用重点实验室,南宁,530005%南宁中诺生物工程有限公司,南宁,530005</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>WU4</scope><scope>~WA</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>2005</creationdate><title>弗氏柠檬酸菌甘油脱水酶基因在大肠杆菌中的克隆和表达</title><author>齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c583-5b633182331cec063c20d59b918b246a35618366117000672c91692147ac5f383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi</language><creationdate>2005</creationdate><topic>SDS-PAGE</topic><topic>克隆</topic><topic>克隆和表达</topic><topic>基因组DNA</topic><topic>大肠杆菌</topic><topic>弗氏柠檬酸菌</topic><topic>柠檬酸</topic><topic>甘油脱水酶</topic><topic>表达</topic><topic>酶基因</topic><toplevel>online_resources</toplevel><creatorcontrib>齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-自然科学</collection><collection>中文科技期刊数据库-自然科学-生物科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Gongye weishengwu</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>齐向辉 朱绮霞 韦宇拓 黄鲲 黄日波</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>弗氏柠檬酸菌甘油脱水酶基因在大肠杆菌中的克隆和表达</atitle><jtitle>Gongye weishengwu</jtitle><addtitle>Industrial Microbiology</addtitle><date>2005</date><risdate>2005</risdate><volume>35</volume><issue>3</issue><spage>10</spage><epage>13</epage><pages>10-13</pages><issn>1001-6678</issn><abstract>以弗氏柠檬酸菌(Citrobacter freundii)基因组DNA为模板,通过PCR得到甘油脱水酶(glycerol dehydratase)基因dhaB、dhaC、dhaE,克隆到表达载体pSE380上,得到重组质粒pSn-dhaBCE。将此重组质粒转化到E.coli JM109中,重组菌株SDS-PAGE结果显示有明显的61kD、22kD、16kD三条特异性蛋白条带出现。重组菌株经诱导表达,酶活力为11.59U/mL。</abstract><pub>广西大学广西亚热带生物资源保护利用重点实验室,南宁,530005%南宁中诺生物工程有限公司,南宁,530005</pub><doi>10.3969/j.issn.1001-6678.2005.03.003</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1001-6678 |
ispartof | Gongye weishengwu, 2005, Vol.35 (3), p.10-13 |
issn | 1001-6678 |
language | chi |
recordid | cdi_wanfang_journals_gywsw200503003 |
source | Alma/SFX Local Collection |
subjects | SDS-PAGE 克隆 克隆和表达 基因组DNA 大肠杆菌 弗氏柠檬酸菌 柠檬酸 甘油脱水酶 表达 酶基因 |
title | 弗氏柠檬酸菌甘油脱水酶基因在大肠杆菌中的克隆和表达 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T21%3A05%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wanfang_jour_chong&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=%E5%BC%97%E6%B0%8F%E6%9F%A0%E6%AA%AC%E9%85%B8%E8%8F%8C%E7%94%98%E6%B2%B9%E8%84%B1%E6%B0%B4%E9%85%B6%E5%9F%BA%E5%9B%A0%E5%9C%A8%E5%A4%A7%E8%82%A0%E6%9D%86%E8%8F%8C%E4%B8%AD%E7%9A%84%E5%85%8B%E9%9A%86%E5%92%8C%E8%A1%A8%E8%BE%BE&rft.jtitle=Gongye%20weishengwu&rft.au=%E9%BD%90%E5%90%91%E8%BE%89%20%E6%9C%B1%E7%BB%AE%E9%9C%9E%20%E9%9F%A6%E5%AE%87%E6%8B%93%20%E9%BB%84%E9%B2%B2%20%E9%BB%84%E6%97%A5%E6%B3%A2&rft.date=2005&rft.volume=35&rft.issue=3&rft.spage=10&rft.epage=13&rft.pages=10-13&rft.issn=1001-6678&rft_id=info:doi/10.3969/j.issn.1001-6678.2005.03.003&rft_dat=%3Cwanfang_jour_chong%3Egywsw200503003%3C/wanfang_jour_chong%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_cqvip_id=20186471&rft_wanfj_id=gywsw200503003&rfr_iscdi=true |