Dalessandro G, Northcote D H
Biochem J. 1977 Feb 15;162(2):281-8. doi: 10.1042/bj1620281.
A protein fraction [precipitate obtained between 40 and 65% (NH4)2SO4 satn.] prepared from cambial cells, differentiating xylem cells and differentiated xylem cells of pine and fir trees contained all the enzymes required for the nucleoside diphosphate sugar interconversions. By using UDP-D-[U-14C]glucose or UDP-D-[U-14C]galactose, UDP-D-[U-14C-]glucuronic acid and UDP-D-[U-14C]xylose as substrates, the activities of UDP-D-galactose 4-epimerase (DC 5.1.3.2), UDP-D-xylose 4-epimerase(EC 5.1.3.5), UDP-D-glucose dehydrogenase (EC 1.1.1.22) and UDP-D-glucuronate 4-epimerase (EC5.1.3.6), UDP-d-glucuronate decarboxylase (EC 4.1.1.35) were measured at different stages of cell-wall development. The specific activities and the activities per cell of these enzymes varied during differentiation of cambium to xylem according to the type polysaccharide synthesized. Variations were also found between the two species investigated. These data, compared with those obtained in out previous work on angiosperms [see the preceding paper, Dalessandro & Northcote (1977) Biochem. J. 162, 267-279], suggest that some control of polysaccharide synthesis operates at the level of the formation of the precursors of pectin and hemicellulose syntheses.
从松树和冷杉树的形成层细胞、正在分化的木质部细胞以及已分化的木质部细胞中制备的一种蛋白质组分(在40%至65%饱和度的硫酸铵中获得的沉淀)含有核苷二磷酸糖相互转化所需的所有酶。以UDP-D-[U-¹⁴C]葡萄糖、UDP-D-[U-¹⁴C]半乳糖、UDP-D-[U-¹⁴C-]葡萄糖醛酸和UDP-D-[U-¹⁴C]木糖为底物,在细胞壁发育的不同阶段测定了UDP-D-半乳糖4-表异构酶(DC 5.1.3.2)、UDP-D-木糖4-表异构酶(EC 5.1.3.5)、UDP-D-葡萄糖脱氢酶(EC 1.1.1.22)、UDP-D-葡萄糖醛酸4-表异构酶(EC5.1.3.6)和UDP-D-葡萄糖醛酸脱羧酶(EC 4.1.1.35)的活性。这些酶的比活性和每个细胞的活性在形成层向木质部分化过程中,根据合成的多糖类型而有所不同。在所研究的两个物种之间也发现了差异。这些数据与我们之前关于被子植物的研究结果[见前文,Dalessandro & Northcote(1977)Biochem. J. 162, 267 - 279]相比,表明在果胶和半纤维素合成前体的形成水平上存在对多糖合成的某种控制。