Cloning and characterization of a sucrose synthase-encoding gene from muskmelon

被引:18
|
作者
Wen, Xiaoxia [1 ]
Zhang, Wenqian [1 ]
Feng, Yanqing [1 ]
Yu, Xiyan [1 ]
机构
[1] Shandong Agr Univ, State Key Lab Crop Biol, Coll Hort Sci & Engn, Tai An 271018, Shandong, Peoples R China
关键词
Cucumis melo; CmSS1; Gene expression; Sucrose metabolism; PHOSPHATE SYNTHASE; TOMATO FRUIT; ACID INVERTASE; EXPRESSION; METABOLISM; ACCUMULATION; STARCH; ENZYMES; MAIZE; ARABIDOPSIS;
D O I
10.1007/s11033-009-9539-x
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
A full-length cDNA clone encoding sucrose synthase (SS; EC 2.4.1.13) was isolated from muskmelon (Cucumis melo L.) by RT-PCR and RACE. The clone, designated as CmSS1, contains 2,585 nucleotides with an open reading frame of 2,412 nucleotides. The deduced 804 amino acid sequence showed high identities with other plant sucrose synthase. Real time PCR analysis indicated that CmSS1 expression differed among root, stem, leaf, flower and fruit tissues. The analysis during fruit development indicated that CmSS1 mRNA showed its maximum level at 5 days after pollination (DAP) and decreased gradually during fruit development until its minimum level in mature fruit. The sucrose content was very low in fruit before 20 DAP but increased dramatically between 20 and 30 DAP during fruit development. However, SS activities in both direction of sucrose synthesis and sucrose cleavage were very low and changed little during fruit development, suggesting that SS may play little role in determining sucrose accumulation during muskmelon fruit.
引用
收藏
页码:695 / 702
页数:8
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