Preger Valeria, Scagliarini Sandra, Pupillo Paolo, Trost Paolo
Laboratory of Molecular Plant Physiology, Department of Biology, University of Bologna, Via Irnerio 42, 40126 Bologna, Italy.
Planta. 2005 Jan;220(3):365-75. doi: 10.1007/s00425-004-1360-0. Epub 2004 Sep 9.
Two membrane-bound, ascorbate-dependent b-type cytochromes were identified in etiolated bean (Phaseolus vulgaris L.) hypocotyls. Following solubilization of microsomal membranes and anion-exchange chromatography at pH 8.0, two major cytochrome peaks (P-I and P-II) were separated. Both cytochromes were reduced by ascorbate and re-oxidized by monodehydroascorbate, but P-I reduction by ascorbate was higher and saturated at far lower concentrations of ascorbate with respect to P-II. The alpha-band was symmetrically centered at 561 nm in P-I, but it was asymmetric in P-II with a maximum at 562 nm and shoulder at 557 nm. Ascorbate reduction of P-II, but not P-I, was inhibited by diethyl pyrocarbonate. Reduced P-II but not P-I was readily oxidized by certain ferric chelates, including FeEDTA and Fe-nitrilotriacetic acid. Purified P-I, associated with the plasma membrane, showed up as a 63-kDa glycosylated protein during sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and behaved as a monomer of about 70 kDa during size-exclusion chromatography. P-I identified with a previously purified ascorbate-dependent b-type cytochrome of bean hypocotyl plasma membranes. Partially purified P-II, on the other hand, correlated with a heme-protein of 27 kDa in SDS-PAGE gels, was dimeric (60 kDa) during size-exclusion chromatography, and was associated with the tonoplast marker V-ATPase in sucrose gradients. The sequence of a peptide of 11 residues obtained by tryptic digestion of P-II was found to be identical to a segment of a putative cytochrome b561 of Zea mays and highly conserved in other related plant sequences, including that of Arabidopsis thaliana cytochrome b561-1 (CAA18169). The biochemical features fully support the assignment of P-II cytochrome to the family of cytochrome b561, ascorbate-dependent (CYBASC) cytochromes, which also includes cytochrome b561 of animal chromaffin granules. The presence of a cytochrome reducing ferric chelates on the tonoplast is consistent with the role of plant vacuoles in iron homeostasis.
在黄化菜豆(菜豆)下胚轴中鉴定出两种膜结合的、依赖抗坏血酸的b型细胞色素。微粒体膜溶解后,在pH 8.0条件下进行阴离子交换色谱分析,分离出两个主要的细胞色素峰(P-I和P-II)。两种细胞色素都能被抗坏血酸还原,并被单脱氢抗坏血酸重新氧化,但相对于P-II,抗坏血酸对P-I的还原作用更强,且在低得多的抗坏血酸浓度下就达到饱和。P-I的α带在561 nm处对称居中,而P-II的α带不对称,最大值在562 nm,肩峰在557 nm。焦碳酸二乙酯抑制抗坏血酸对P-II的还原,但不抑制对P-I的还原。还原态的P-II能被某些铁螯合物(包括FeEDTA和Fe-次氮基三乙酸)迅速氧化,而还原态的P-I则不能。与质膜相关的纯化P-I在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)中显示为一种63 kDa的糖基化蛋白,在尺寸排阻色谱中表现为约70 kDa的单体。P-I与先前纯化的菜豆下胚质膜抗坏血酸依赖性b型细胞色素一致。另一方面,部分纯化的P-II在SDS-PAGE凝胶中与一种27 kDa的血红素蛋白相关,在尺寸排阻色谱中为二聚体(60 kDa),并在蔗糖梯度中与液泡膜标记物V-ATPase相关。通过胰蛋白酶消化P-II获得的一个11个残基的肽段序列与玉米假定的细胞色素b561的一个片段相同,并且在其他相关植物序列(包括拟南芥细胞色素b561-1(CAA18169))中高度保守。这些生化特征充分支持将P-II细胞色素归为细胞色素b561家族,即依赖抗坏血酸的(CYBASC)细胞色素,该家族还包括动物嗜铬粒的细胞色素b561。液泡膜上存在还原铁螯合物的细胞色素与植物液泡在铁稳态中的作用一致。