Genome-Wide Identification, 3D Modeling, Expression and Enzymatic Activity Analysis of Cell Wall Invertase Gene Family from Cassava (Manihot esculenta Crantz)

被引:37
作者
Yao, Yuan [1 ]
Geng, Meng-Ting [1 ]
Wu, Xiao-Hui [2 ]
Liu, Jiao [1 ]
Li, Rui-Mei [1 ]
Hu, Xin-Wen [2 ]
Guo, Jian-Chun [1 ]
机构
[1] Chinese Acad Trop Agr Sci, Inst Trop Biosci & Biotechnol, Key Lab Biol & Genet Resources Trop Crops, Minist Agr, Haikou 571101, Peoples R China
[2] Hainan Univ, Coll Agr, Haikou 571104, Peoples R China
基金
中国国家自然科学基金;
关键词
molecular cloning; cell wall invertase; cassava; gene expression analysis; 3D modeling; enzyme activities; MONOSACCHARIDE TRANSPORTER; ARABIDOPSIS-THALIANA; VACUOLAR INVERTASE; SUCROSE; TOMATO; STRESS; POTATO; GROWTH; MAIZE; INHIBITION;
D O I
10.3390/ijms15057313
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cell wall invertases play a crucial role on the sucrose metabolism in plant source and sink organs. In this research, six cell wall invertase genes (MeCWINV1-6) were cloned from cassava. All the MeCWINVs contain a putative signal peptide with a predicted extracellular location. The overall predicted structures of the MeCWINV1-6 are similar to AtcwINV1. Their N-terminus domain forms a beta-propeller module and three conserved sequence domains (NDPNG, RDP and WECP(V)D), in which the catalytic residues are situated in these domains; while the C-terminus domain consists of a beta-sandwich module. The predicted structure of Pro residue from the WECPD (MeCWINV1, 2, 5, and 6), and Val residue from the WECVD (MeCWINV3 and 4) are different. The activity of MeCWINV1 and 3 were higher than other MeCWINVs in leaves and tubers, which suggested that sucrose was mainly catalyzed by the MeCWINV1 and 3 in the apoplastic space of cassava source and sink organs. The transcriptional levels of all the MeCWINVs and their enzymatic activity were lower in tubers than in leaves at all the stages during the cassava tuber development. It suggested that the major role of the MeCWINVs was on the regulation of carbon exportation from source leaves, and the ratio of sucrose to hexose in the apoplasts; the role of these enzymes on the sucrose unloading to tuber was weaker.
引用
收藏
页码:7313 / 7331
页数:19
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