Hampp R, Outlaw W H, Tarczynski M C
Department of Biological Science (Unit I), Florida State University, Tallahassee, Florida 32306.
Plant Physiol. 1982 Dec;70(6):1582-5. doi: 10.1104/pp.70.6.1582.
Guard cells and three other cell types from Vicia faba L. ;Longpod' leaflets were assayed for enzymes that catalyze one step in each of five major carbon pathways in green plants: the photosynthetic carbon reduction pathway (ribulose-bisphosphate carboxylase, EC 4.1.1.39), the photosynthetic carbon oxidation pathway (hydroxypyruvate reductase, EC 1.1.1.81), glycolysis ([NAD] glyceraldehyde-P dehydrogenase, EC 1.2.1.12), the oxidative pentose-P pathway (6-P-gluconate dehydrogenase, EC 1.1.1.44), and the tricarboxylic acid pathway (fumarase, EC 4.2.1.2). Neither ribulose-bisphosphate carboxylase nor hydroxypyruvate reductase could be detected in guard cells or epidermal cells; high levels of these activities were present in mesophyll cells. The specific activity of fumarase (protein basis) was about 4-fold higher in guard cells than in epidermal, palisade parenchyma or spongy parenchyma cells. (NAD) glyceraldehyde-P and 6-P-gluconate dehydrogenases also were present at high protein specific activities in guard cells (2- to 4-fold that in meosphyll cells).It was concluded that the capacity for metabolite flux through the catabolic pathways is high in guard cells. In addition, other support is provided for the view that photoreduction of CO(2) by these guard cells is absent.
对蚕豆“长荚”小叶中的保卫细胞和其他三种细胞类型进行了检测,以确定催化绿色植物五种主要碳途径中每一步骤的酶:光合碳还原途径(核酮糖-1,5-二磷酸羧化酶,EC 4.1.1.39)、光合碳氧化途径(羟基丙酮酸还原酶,EC 1.1.1.81)、糖酵解([NAD]甘油醛-P脱氢酶,EC 1.2.1.12)、氧化戊糖-P途径(6-P-葡萄糖酸脱氢酶,EC 1.1.1.44)和三羧酸途径(延胡索酸酶,EC 4.2.1.2)。在保卫细胞或表皮细胞中均未检测到核酮糖-1,5-二磷酸羧化酶或羟基丙酮酸还原酶;这些活性在叶肉细胞中含量很高。延胡索酸酶的比活性(以蛋白质计)在保卫细胞中比在表皮、栅栏薄壁组织或海绵薄壁组织细胞中高约4倍。(NAD)甘油醛-P脱氢酶和6-P-葡萄糖酸脱氢酶在保卫细胞中的蛋白质比活性也很高(是叶肉细胞中的2至4倍)。得出的结论是,保卫细胞中通过分解代谢途径的代谢物通量能力很高。此外,为这些保卫细胞不存在CO₂光还原的观点提供了其他支持。