Department of Biological Science (Unit I), Florida State University, Tallahassee, Florida 32306.
Plant Physiol. 1982 Oct;70(4):1218-20. doi: 10.1104/pp.70.4.1218.
Guard cell pairs were dissected from freeze-dried leaves of plants representing 15 families, including monocots, dicots, and pteridophytes. All three major photosynthetic carbon pathways (C(2), C(4), and Crassulacean acid metabolism) were represented. These individual guard cell pairs were assayed quantitatively for ribulose-1,5-bisphosphate carboxylase specific activity. Assay sensitivity averaged 0.08 picomoles of ribulose-P(2) dependent P-glycerate formation (i.e. 100-fold more sensitive than required to detect the activity present in a single Vicia faba mesophyll cell). The calculated specific activities for guard cells and mesophyll cells averaged 4 and 472 millimoles per kilogram dry weight per hour, respectively. For all species surveyed, (a) the enzyme activity calculated for guard cells was below the detection limit of the assay, or (b) the specific activity (weight or cell basis) calculated for guard cells was less than 1% of the specific activity calculated for adjacent mesophyll cells. Based on this survey, the generalization is made that the photosynthetic carbon reduction pathway is absent, or virtually so, in guard cell chloroplasts.
从代表 15 个科的植物的冻干叶片中分离出保卫细胞对,包括单子叶植物、双子叶植物和蕨类植物。所有三种主要的光合作用碳代谢途径(C(2)、C(4)和景天酸代谢)都有代表。对这些单个的保卫细胞对进行定量测定,以测定核酮糖-1,5-二磷酸羧化酶的比活。测定的平均灵敏度为 0.08 皮摩尔核酮糖-P(2)依赖性 P-甘油酸形成(即比检测单个蚕豆叶片细胞中存在的活性所需的灵敏度高 100 倍)。计算出的保卫细胞和叶肉细胞的比活分别为每公斤干重每小时 4 和 472 毫摩尔。对于所有调查的物种,(a)计算出的保卫细胞的酶活性低于测定的检测限,或者(b)计算出的保卫细胞的比活(重量或细胞基础)低于计算出的相邻叶肉细胞的比活的 1%。基于这项调查,可以得出这样的结论,即光合作用碳还原途径在保卫细胞的叶绿体中不存在,或者几乎不存在。