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Genome-wide identification, 3D modeling, expression and enzymatic activity analysis of cell wall invertase gene family from cassava (Manihot esculenta Crantz).
Yao, Yuan; Geng, Meng-Ting; Wu, Xiao-Hui; Liu, Jiao; Li, Rui-Mei; Hu, Xin-Wen; Guo, Jian-Chun.
  • Yao Y; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China. yaofaraway1@163.com.
  • Geng MT; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China. mengtinggeng8908@163.com.
  • Wu XH; Agricultural College of Hainan University, Haikou 571104, China. ficz@163.com.
  • Liu J; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China. liujiao@itbb.org.cn.
  • Li RM; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China. liruimei@itbb.org.cn.
  • Hu XW; Agricultural College of Hainan University, Haikou 571104, China. huxinwen@hainu.edu.cn.
  • Guo JC; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China. jianchunguoh@163.com.
Int J Mol Sci ; 15(5): 7313-31, 2014 Apr 28.
Article en En | MEDLINE | ID: mdl-24786092
ABSTRACT
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 ß-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 ß-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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Manihot / Regulación Enzimológica de la Expresión Génica / Pared Celular / Regulación de la Expresión Génica de las Plantas / Beta-Fructofuranosidasa Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Manihot / Regulación Enzimológica de la Expresión Génica / Pared Celular / Regulación de la Expresión Génica de las Plantas / Beta-Fructofuranosidasa Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Año: 2014 Tipo del documento: Article