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油菜叶绿体乙酰辅酶A羧化酶单交换表达载体的构建(PDF)

《广西植物》[ISSN:1000-3142/CN:45-1134/Q]

期数:
2015年04期
页码:
609-617
栏目:
植物生理与分子生物学
出版日期:
2015-07-20

文章信息/Info

Title:
Costruction of single-cross expression vector for chloroplast acetyl coenzyme A carboxylase in Brassica napus
文章编号:
1000-3142(2015)04-0609-09
作者:
武玉永1 谭秀华1 马立新2*
1. 滨州医学院 医学遗传学教研室, 山东 烟台 264003; 2. 湖北大学 生命科学学院 分子微生物学与基因工程实验室, 武汉 430062
Author(s):
WU Yu-Yong1 TAN Xiu-Hua1 MA Li-Xin2*
1. Department of Medical Genetics, Binzhou Medical University, Yantai 264003, China; 2. College of Life Sciences, Hubei University, Molecular Microbiology and Genetic Engineering Laboratory, Wuhan 430062, China
关键词:
油菜 叶绿体 乙酰辅酶A羧化酶 单交换 表达载体 构建
Keywords:
Brassica napus chloroplast acetyl coenzyme A carboxylase single-cross expression vector construction
分类号:
Q943.2; S565.4
DOI:
10.11931/guihaia.gxzw201405026
文献标识码:
A
摘要:
根据已知序列设计引物,通过PCR扩增获得质体定位的乙酰辅酶A羧化酶的4个亚基的基因序列。先将该酶4个亚基的基因进行拼接,然后将这4个拼接好的片段,克隆到pMD18-T载体上,得到质粒pHBM714。再以质粒pHBM714 DNA为模板,用分别带有Cpo I和Asc I酶切位点的引物进行PCR扩增,PCR产物在dTTP的保护下经T4 DNA聚合酶处理,与将质粒pHBM720 DNA纯化后经Cpo I和Asc I双酶切后得到的大片段连接,连接产物转化大肠杆菌Xl10-gold,得到正确的重组子命名为pHBM726。此质粒pHBM726,即为带有壮观霉素抗性基因(aadA)筛选标记的质体定位的乙酰辅酶A羧化酶基因油菜叶绿体单交换表达载体; 在此载体中壮观霉素抗性基因(aadA)、乙酰辅酶A羧化酶的4个亚基的基因(ACC)和绿色荧光蛋白基因(gfp)共6个基因串联在一起,共用一个启动子序列,一起来进行表达; 通过酶切检测、PCR验证和测序验证,均表明该表达载体构建成功。最后此载体在大肠杆菌中表达时,发现重组菌能够在含壮观霉素的培养基上生长,且在可见光下,能看到绿色荧光,表明壮观霉素抗性基因和绿色荧光蛋白基因均在大肠杆菌中成功表达; 表达产物通过Western印迹验证表明组成乙酰辅酶A羧化酶的4个亚基的基因在大肠杆菌中成功表达。以上结果表明,该表达载体中串联排列的这6个基因均在大肠杆菌中成功表达。该研究结果可为质体定位的乙酰辅酶A羧化酶转叶绿体的研究奠定基础,为油菜油脂代谢研究提供参考。
Abstract:
This study aimed to construct Brassica napus chloroplast acetyl coenzyme A carboxylase single cross-over expression vector,to lay the foundation for chloroplast transformation research of B. napus acetyl coenzyme A carboxylase,at the same time,to provide a good reference for the research of oilrape lipid metabolism. According to the known sequences form GenBank,the corresponding primers were designed,the gene sequences of four subunits for plastid acetyl coenzyme A carboxylase were amplified by Polymerase chain reaction. The form of acetyl coenzyme A carboxylase of Escherichia coli and the form of acetyl coenzyme A carboxylase of plastid were similar,therefore the gene sequences of four subunits of plastid acetyl coenzyme A carboxylase were spliced according to the form of acetyl coenzyme A carboxylase of Escherichia coli. And the plasmid pHBM714 was obtained by cloned the gene fragments of chloroplast acetyl coenzyme A carboxylase into pMD18-T vector. Then the DNA sequence of plasmid pHBM714 was taken as the templaste,and the front of primers were added to the gene sequence of restriction enzyme sites of Cpo I and the gene sequence of restriction enzyme sites of Asc I respectively. At last,the sequence of chloroplast acetyl coenzyme A carboxylase was amplified by Polymerase chain reaction. These products of Polymerase chain reaction were processed by T4 DNA polymerase in the protection of dTTP,and which was jointed with the larget fragment that was got by the plasmid of pHBM720 DNA digested by restriction enzyme of Cpo I and restriction enzyme of Asc I. The ligation products was transformed into Escherichia coli Xl10-gold. The recombinant that was verified by amplification of Polymerase chain reaction and restriction enzymes digested correctly was named the plasmid of pHBM726. The recombinant plasmid of pHBM726 was the single cross-over expression vector for chloroplast acetyl coenzyme A carboxylase in Brassica napus which was obtained with selection marker of spectinomycin resistance gene(aadA)(-Prrn-SD-aadA-ACC-gfp-psbA3’-RbcL-Ampr+Ori -ACCD-). And it consisted of spectinomycin resistance gene(aadA),biotin carboxylase gene(BC),biotin carboxyl carrier protein gene(BP4),carboxyltransferase beta subunit gene(β-CT),carboxyl transferase alpha subunit gene(α-CT)and green fluorescent protein gene(gfp),furthermore,the six genes that were connected in series,and these genes which were expressed together with a common promoter sequence in Escherichia coli. The plasmid of pHBM726 was constructed successfully that were verified by restriction enzyme digestion,Polymerase chain reaction and sequencing. Finally,the recombinant plasmid of pHBM726 was expressed in Escherichia coli,with the recombinant plasmid pHBM726 of Escherichia coli could grow well on the medium plate containing spectinomycin,and the single colony was able to emit green fluorescence under visible light excitation,which indicated that spectinomycin resistance gene and green fluorescent protein gene were expressed successfully in Escherichia coli; the expression products of four subunits of plastid targeted acetyl coenzyme A carboxylase gene were all detected by Western blotting,it showed that four subunits of plastid targeted acetyl coenzyme A carboxylase gene were expressed successfully in Escherichia coli. All the results showed that four subunits of plastid targeted acetyl coenzyme A carboxylase gene,spectinomycin resistance gene and green fluorescent protein gene which were successfully expressed in Escherichia coli. This study constructed single cross-over expression vector for Brassica napus chloroplast acetyl coenzyme A carboxylase,and will lay the solid foundation for the chloroplast transformation research of Brassica napus.

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备注/Memo

备注/Memo:
收稿日期: 2014-09-30修回日期: 2014-12-15
基金项目: 国家“973”重大科学研究计划项目(2013CB910801); 山东省自然科学基金(ZR2010HQ054); 烟台市科技发展计划项目(2013ZH097)。
作者简介: 武玉永(1975-),男,山东沂水人,硕士,讲师,主要从事分子微生物学及植物分子生物学研究,(E-mail)wuyuyong_820@126.com。
*通讯作者: 马立新,教授,主要从事合成生物学与工业生物技术的研究,(E-mail)malixin@hubu.edu.cn。
更新日期/Last Update: 2015-08-27