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大豆(Glycine max (L.) Merr.)植酸酶基因Sphy1 的鉴定及其分子特征研究

Isolation and Characterization of a Phytase Gene (Sphy1) from Soybean (Glycine max (L.) Merr.)

中文摘要英文摘要

在萌发的大豆(Glycine max (L.) Merr. cv. Kefeng6) 子叶中,克隆了1个新型大豆植酸酶基因Sphy1。Sphy1的The cDNA全长为 1644 bp,编码 547 个氨基酸残基。在氨基酸序列的N-端,含有一个由27 氨基酸残基组成的信号肽序列。系统进化分析表明,Sphy1与源于蒺藜苜蓿(M. truncatula )和水稻的植酸酶基因以及蒺藜苜蓿和拟南芥的酸性磷酸酶基因具有较高的同源性。对Sphy1在原核宿主BL21的表达结果表明,表达蛋白具有降解植酸酶的催化活性。对Sphy1的组织表达特性研究发现,该基因在子叶、幼苗叶、茎和根中均有表达,且转录本的数量多少与苗期上述组织中的植酸酶活性强弱密切相关。Sphy1在5 d至30 d幼苗子叶中的表达具有不断增强特性,暗示该基因可能在幼苗生长前期降解子叶中贮存的含磷有机物植酸盐中具有重要作用。

novel phytase gene Sphy1 was isolated based on screening a cDNA library which was constructed from germinated soybean (Glycine max (L.) Merr. cv. Kefeng6) cotyledon. The full-length cDNA of Sphy1 was 1 644 bp predicated to encode 547 amino acids including an N terminal signal peptide of 27 amino acids. Phylogenetic analysis indicated that Sphy1 had high similarities with the phytase genes from M. truncatula and rice, and acid phosphatase genes from M. truncatula and Arabidopsis. Prokaryotic expression of Sphy1 in BL21 showed that the induced protein had high phytase activities. The transcripts of Sphy1 could be detected in various tissues, such as cotyledons, leaves, stems and roots of seedlings. The phytase activities in the above tissues were accordance with their corresponding Sphy1 transcripts. The transcripts of Sphy1 in cotyledons showed an increasing trend from 5 to 30 days after germination, suggesting that Sphy1 had involved the hydrolyses of the organic phosphorus compounds in seeds from the stages of early seed germination to young seedlings in soybean. Therefore, it is speculated that Sphy1 plays an important role during the seed germination and the growth of the seedlings by releasing inorganic phosphorus (Pi) from phosphorus reserve in seeds.

王娇娇、肖凯、郭丽

分子生物学植物学遗传学

大豆(Glycine max (L.) Merr.)植酸酶基因Sphy1基因表达植酸酶活性

Soybean (Glycine max (L.) Merr.)Phytase geneSphy1Gene expressionPhytase activity

王娇娇,肖凯,郭丽.大豆(Glycine max (L.) Merr.)植酸酶基因Sphy1 的鉴定及其分子特征研究[EB/OL].(2009-12-17)[2025-05-02].http://www.paper.edu.cn/releasepaper/content/200912-547.点此复制

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