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在黑暗中生长的大豆幼苗茎中含有丰富的与叶糖蛋白同源的蛋白质。蛋白质和 cDNA 的分析。

Proteins homologous to leaf glycoproteins are abundant in stems of dark-grown soybean seedlings. Analysis of proteins and cDNAs.

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, 77843, College Station, TX, USA.

出版信息

Plant Mol Biol. 1988 Nov;11(6):845-56. doi: 10.1007/BF00019524.

Abstract

We report here the cloning and sequence analysis of cDNAs for a pair of closely related proteins from soybean (Glycine max [L.] Merr. cv. Williams 82) stems. Both proteins are abundant in soluble extracts of seedling stems but not of roots. One of these proteins (M r=28 kDa) is also foundd in the cell wall fraction of stems and actumulates there when seedlings are exposed to mild water deficit for 48 h. The mRNA for these proteins is most abundant in the stem region which contains dividing cells, less abundant in elongating and mature stem cells, and rare in roots. Using antiserum against the 28 kDa protein, we isolated cDNA clones encoding it and an antigenically related 31 kDa protein. The two cDNAs are 80% homologous in nucleotide and amino acid coding sequence. The predicted proteins have similar hydropathy profiles, and contain putative NH2-terminal signal sequences and a single putative N-linked glycosylation site. The two proteins differ significantly in calculated pI (28 kDa=8.6; 31 kDa=5.8), and the charge difference is demonstrated on two-dimensional gels. The proteins described here may function as somatic storage proteins during early seedling development, and are closely related to glycoproteins which accumulate in vacuoles of paraveinal mesophyll cells of fully expanded soybean leaves when plants are depodded.

摘要

我们在这里报告了一对来自大豆(Glycine max [L.] Merr. cv. Williams 82)茎的密切相关的蛋白质的 cDNA 的克隆和序列分析。这两种蛋白质在幼苗茎的可溶性提取物中含量丰富,但在根中不丰富。其中一种蛋白质(Mr=28 kDa)也存在于茎的细胞壁部分,当幼苗暴露在轻度水分亏缺 48 小时时,它会在那里积累。这些蛋白质的 mRNA 在含有分裂细胞的茎区最为丰富,在伸长和成熟的茎细胞中较少,在根中很少。使用针对 28 kDa 蛋白的抗血清,我们分离出编码它和一种抗原相关的 31 kDa 蛋白的 cDNA 克隆。这两个 cDNA 在核苷酸和氨基酸编码序列上有 80%的同源性。预测的蛋白质具有相似的疏水性图谱,并且含有推定的 NH2-末端信号序列和一个单一的推定的 N-连接糖基化位点。这两种蛋白质在计算的 pI(28 kDa=8.6;31 kDa=5.8)上有显著差异,并且在二维凝胶上显示出电荷差异。这里描述的蛋白质可能在早期幼苗发育期间作为体细胞储存蛋白发挥作用,并且与当植物去荚时完全展开的大豆叶片的侧脉间叶肉细胞的液泡中积累的糖蛋白密切相关。

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