Flechner A, Dressen U, Westhoff P, Henze K, Schnarrenberger C, Martin W
Institut für Pflanzenphysiologie, Berlin, Germany.
Plant Mol Biol. 1996 Nov;32(3):475-84. doi: 10.1007/BF00019099.
A cDNA encoding the Calvin cycle enzyme transketolase (TKL; EC 2.2.1.1) was isolated from Sorghum bicolor via subtractive differential hybridization, and used to isolate several full-length cDNA clones for this enzyme from spinach. Functional identity of the encoded mature subunit was shown by an 8.6-fold increase of TKL activity upon induction of Escherichia coli cells that overexpress the spinach TKL subunit under the control of the bacteriophage T7 promoter. Chloroplast localization of the cloned enzyme is shown by processing of the in vitro synthesized precursor upon uptake by isolated chloroplasts. Southern blot-analysis suggests that TKL is encoded by a single gene in the spinach genome. TKL proteins of both higher-plant chloroplasts and the cytosol of non-photosynthetic eukaryotes are found to be unexpectedly similar to eubacterial homologues, suggesting a possible eubacterial origin of these nuclear genes. Chloroplast TKL is the last of the demonstrably chloroplast-localized Calvin cycle enzymes to have been cloned and thus completes the isolation of gene probes for all enzymes of the pathway in higher plants.
通过消减差异杂交从高粱中分离出编码卡尔文循环酶转酮醇酶(TKL;EC 2.2.1.1)的cDNA,并用于从菠菜中分离该酶的几个全长cDNA克隆。在噬菌体T7启动子控制下过表达菠菜TKL亚基的大肠杆菌细胞诱导后,TKL活性增加8.6倍,证明了编码的成熟亚基的功能同一性。分离的叶绿体摄取体外合成的前体后对其进行加工,显示了克隆酶的叶绿体定位。Southern印迹分析表明,TKL由菠菜基因组中的单个基因编码。发现高等植物叶绿体和非光合真核生物细胞质中的TKL蛋白与真细菌同源物意外相似,表明这些核基因可能起源于真细菌。叶绿体TKL是最后一个被克隆的明显定位于叶绿体的卡尔文循环酶,从而完成了高等植物该途径所有酶的基因探针的分离。