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107杨次生木质部PAL基因的RT-PCR扩增及其鉴定
Cloning and Identification of PAL Gene Amplified by RT-PCR from Populus×euramericana cv.“74/76” Second Xylem mRNA
【Abstract】 A fragment of PAL (phenylalanine ammonia_lyase) gene was amplified by RT_PCR from poplar (Populus×euramericana cv. “74/76”) developing second xylem mRNA. It was cloned into pGEM-T Easy vector and identified by restriction enzyme, PCR amplification and sequencing. The sequence of the amplified DNA fragment was 565 base pairs. Alignment with the P. kitakamiensis PAL cDNA sequence retrieved from EMBL nucleotide acid database (accession number D30656) showed that the first 400 base pairs in both sequences were almost identical. Therefore the fragment was part of PAL gene. And both of sense and anti-sense expressional vectors were constructed.
【关键词】 欧美杨107;
苯丙氨酸解氨酶(PAL);
RT-PCR;
载体构建;
【Key words】 Populus×euramericana cv.“74/76"; Phenylalanine ammonia-lyase(PAL); RT-PCR; Vector construction;
【Key words】 Populus×euramericana cv.“74/76"; Phenylalanine ammonia-lyase(PAL); RT-PCR; Vector construction;
【基金】 国家林业局 948项目———控制林木木质素合成酶基因的引进及其转化技术研究 ( 94-4 -2 1)
- 【文献出处】 林业科学 ,Scientia Silvae Sinicae , 编辑部邮箱 ,2004年04期
- 【分类号】Q946
- 【被引频次】32
- 【下载频次】218