Characterization, Expression Profiling, and Functional Analyses of a 4CL-Like Gene of Populus trichocarpa

被引:3
作者
Wei, Hui [1 ]
Xu, Chen [1 ]
Movahedi, Ali [1 ]
Sun, Weibo [1 ]
Qiang Zhuge [1 ]
机构
[1] Nanjing Forestry Univ, Coll Biol & Environm, Minist Educ,Key Lab Forest Genet & Biotechnol, Coinnovat Ctr Sustainable Forestry Southern China, Nanjing 210037, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
ACS; CL; 4CL-like; PTS; box I domain; box II domain; Populus trichocarpa; COENZYME-A SYNTHETASE; ACETYL-COA SYNTHETASE; SUBSTRATE-SPECIFICITY; ARABIDOPSIS-THALIANA; LIGASE; BIOSYNTHESIS; IDENTIFICATION; PURIFICATION; 4-COUMARATE; LIGNIN;
D O I
10.3390/pr7010045
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Adenosine 5 '-monophosphate (AMP) (adenylate)-forming acetyl-CoA synthetase (ACS) catalyzes the formation of acetyl-coenzyme A (CoA), and the ACS family is closely related to the 4-coumarate CoA ligase (4CL) family. In this study, a 4CL-like gene was cloned from Populus trichocarpa and named Pt4CL-like. Characterization of Pt4CL-like, using bioinformatics, showed that it contained box I and box II domains at the end of the C-terminal sequence, and there is a characteristic sequence of ACS, namely, peroxisome-targeting sequence (PTS). Real-time PCR results showed that the 4CL-like gene was expressed in all tissues tested, and was highly expressed in the stems. A denaturation and renaturation process was conducted, and the recombinant Pt4CL-like protein was purified through HisTrap(TM) high performance affinity chromatography. It showed Pt4CL-like protein did not catalyze substrates of 4CL, but could significantly catalyzed sodium acetate. These results indicate that Pt4CL-like protein belongs to the ACS family, providing a theoretical basis for further analysis and comparison of the functions of adenylate-forming enzymes and 4CL family.
引用
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页数:15
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