Boldt Ralf, Edner Christoph, Kolukisaoglu Uner, Hagemann Martin, Weckwerth Wolfram, Wienkoop Stefanie, Morgenthal Katja, Bauwe Hermann
University of Rostock, Bioscience Institute, Plant Physiology Department, D-18051 Rostock, Germany.
Plant Cell. 2005 Aug;17(8):2413-20. doi: 10.1105/tpc.105.033993. Epub 2005 Jun 24.
D-GLYCERATE 3-KINASE (GLYK; EC 2.7.1.31) catalyzes the concluding reaction of the photorespiratory C2 cycle, an indispensable ancillary metabolic pathway to the photosynthetic C3 cycle that enables land plants to grow in an oxygen-containing atmosphere. Except for GLYK, all other enzymes that contribute to the C2 cycle are known by their primary structures, and the encoding genes have been identified. We have purified and partially sequenced this yet missing enzyme from Arabidopsis thaliana and identified it as a putative kinase-annotated single-copy gene At1g80380. The exclusive catalytic properties of the gene product were confirmed after heterologous expression in Escherichia coli. Arabidopsis T-DNA insertional knockout mutants show no GLYK activity and are not viable in normal air; however, they grow under elevated CO2, providing direct evidence of the obligatory nature of the ultimate step of the C2 cycle. The newly identified GLYK is both structurally and phylogenetically distinct from known glycerate kinases from bacteria and animals. Orthologous enzymes are present in other plants, fungi, and some cyanobacteria. The metabolic context of GLYK activity in fungi and cyanobacteria remains to be investigated.
D-甘油酸3-激酶(GLYK;EC 2.7.1.31)催化光呼吸C2循环的最后一步反应,光呼吸C2循环是光合C3循环不可或缺的辅助代谢途径,使陆地植物能够在含氧大气中生长。除了GLYK之外,参与C2循环的所有其他酶的一级结构均已明确,其编码基因也已得到鉴定。我们已从拟南芥中纯化出这种缺失的酶并进行了部分测序,将其鉴定为一个推定的带有激酶注释的单拷贝基因At1g80380。在大肠杆菌中进行异源表达后,证实了该基因产物独特的催化特性。拟南芥T-DNA插入敲除突变体无GLYK活性,在正常空气中无法存活;然而,它们在高浓度二氧化碳条件下能够生长,这为C2循环最后一步的必要性提供了直接证据。新鉴定出的GLYK在结构和系统发育上均与细菌和动物中已知的甘油酸激酶不同。其他植物、真菌和一些蓝细菌中存在直系同源酶。真菌和蓝细菌中GLYK活性的代谢背景仍有待研究。