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绿竹(Bambusa oldhamii)转化酶同工酶的分子克隆与功能鉴定

Molecular cloning and functional identification of invertase isozymes from green bamboo Bambusa oldhamii.

作者信息

Hsieh Chang-Wen, Liu Li-Ka, Yeh Sheng-Hsiung, Chen Chi-Fu, Lin Hsin-I, Sung Hsien-Yi, Wang Ai-Yu

机构信息

Institute of Microbiology and Biochemistry, National Taiwan University, Taipei 106, Taiwan.

出版信息

J Agric Food Chem. 2006 Apr 19;54(8):3101-7. doi: 10.1021/jf052711s.

Abstract

Three Bo beta fruct cDNAs encoding acid invertases were cloned from shoots of the green bamboo Bambusa oldhamii. On the basis of the amino acid sequences of their products and phylogenetic analyses, Bo beta fruct1 and Bo beta fruct2 were determined to encode cell wall invertases, whereas Bo beta fruct3encodes a vacuolar invertase. The recombinant proteins encoded by Bo beta fruct2 and Bo beta fruct3 were produced in Pichia pastoris and purified to near homogeneity using ammonium sulfate fractionation and immobilized metal affinity chromatography. The pH optima, pI values, and substrate specificities of the isolated enzymes were consistent with those of plant cell wall or vacuolar invertases. The growth-dependent expression of Bo beta fruct1 and Bo beta fruct2 in the base regions of shoots underscores their roles in sucrose unloading and providing substrates for shoot growth. Its high sucrose affinity suggests that the Bo beta fruct2-encoded enzyme is important for maintaining the sucrose gradient between source and sink organs, while the predominant expression of Bo beta fruct3 in regions of active cell differentiation and expansion suggests functions in osmoregulation and cell enlargement.

摘要

从绿竹(Bambusa oldhamii)的嫩枝中克隆出了三个编码酸性转化酶的Bo beta fruct cDNA。根据其产物的氨基酸序列和系统发育分析,确定Bo beta fruct1和Bo beta fruct2编码细胞壁转化酶,而Bo beta fruct3编码液泡转化酶。由Bo beta fruct2和Bo beta fruct3编码的重组蛋白在毕赤酵母中产生,并通过硫酸铵分级分离和固定化金属亲和色谱法纯化至接近均一。分离出的酶的最适pH值、pI值和底物特异性与植物细胞壁或液泡转化酶的一致。Bo beta fruct1和Bo beta fruct2在嫩枝基部区域的生长依赖性表达突出了它们在蔗糖卸载以及为嫩枝生长提供底物方面的作用。其高蔗糖亲和力表明,由Bo beta fruct2编码的酶对于维持源器官和库器官之间的蔗糖梯度很重要,而Bo beta fruct3在活跃细胞分化和扩展区域的主要表达表明其在渗透调节和细胞扩大方面的功能。

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