Preger Valeria, Tango Nunzio, Marchand Christophe, Lemaire Stéphane D, Carbonera Donatella, Di Valentin Marilena, Costa Alex, Pupillo Paolo, Trost Paolo
Laboratory of Molecular Plant Physiology, Department of Experimental Evolutionary Biology, University of Bologna, Bologna 40126, Italy.
Plant Physiol. 2009 Jun;150(2):606-20. doi: 10.1104/pp.109.139170. Epub 2009 Apr 22.
We report here on the identification of the major plasma membrane (PM) ascorbate-reducible b-type cytochrome of bean (Phaseolus vulgaris) and soybean (Glycine max) hypocotyls as orthologs of Arabidopsis (Arabidopsis thaliana) AIR12 (for auxin induced in root cultures). Soybean AIR12, which is glycosylated and glycosylphosphatidylinositol-anchored to the external side of the PM in vivo, was expressed in Pichia pastoris in a recombinant form, lacking the glycosylphosphatidylinositol modification signal and purified from the culture medium. Recombinant AIR12 is a soluble protein predicted to fold into a beta-sandwich domain and belonging to the DOMON (for dopamine beta-monooxygenase N terminus) domain superfamily. It is shown to be a b-type cytochrome with a symmetrical alpha-band at 561 nm, fully reduced by ascorbate, and fully oxidized by monodehydroascorbate radical. AIR12 is a high-potential cytochrome b showing a wide bimodal dependence from the redox potential between +80 mV and +300 mV. Optical absorption and electron paramagnetic resonance analysis indicate that AIR12 binds a single, highly axial low-spin heme, likely coordinated by methionine-91 and histidine-76, which are strongly conserved in AIR12 sequences. Phylogenetic analyses reveal that the auxin-responsive genes AIR12 represent a new family of PM b-type cytochromes specific to flowering plants. Circumstantial evidence suggests that AIR12 may interact with other redox partners within the PM to constitute a redox link between cytoplasm and apoplast.
我们在此报告,已鉴定出菜豆(Phaseolus vulgaris)和大豆(Glycine max)下胚轴中的主要质膜(PM)抗坏血酸可还原b型细胞色素,它们是拟南芥(Arabidopsis thaliana)AIR12(根培养中生长素诱导基因)的直系同源物。大豆AIR12在体内是糖基化的且通过糖基磷脂酰肌醇锚定在质膜外侧,以重组形式在毕赤酵母中表达,缺少糖基磷脂酰肌醇修饰信号,并从培养基中纯化得到。重组AIR12是一种可溶性蛋白,预计折叠成β-三明治结构域,属于DOMON(多巴胺β-单加氧酶N端)结构域超家族。它被证明是一种b型细胞色素,在561 nm处有对称的α带,能被抗坏血酸完全还原,被单脱氢抗坏血酸自由基完全氧化。AIR12是一种高电位细胞色素b,在+80 mV至+300 mV的氧化还原电位范围内呈现出广泛的双峰依赖性。光吸收和电子顺磁共振分析表明,AIR12结合单个高度轴向的低自旋血红素,可能由甲硫氨酸-91和组氨酸-76配位,这两个氨基酸在AIR12序列中高度保守。系统发育分析表明,生长素响应基因AIR12代表了开花植物特有的质膜b型细胞色素新家族。间接证据表明,AIR12可能与质膜内的其他氧化还原伙伴相互作用,在细胞质和质外体之间构成氧化还原联系。