Fahrendorf T, Ni W, Shorrosh B S, Dixon R A
Plant Biology Division, Samuel Roberts Noble Foundation, Ardmore, OK 73401, USA.
Plant Mol Biol. 1995 Aug;28(5):885-900. doi: 10.1007/BF00042073.
We have isolated cDNA clones encoding the pentose phosphate pathway enzymes 6-phosphogluconate dehydrogenase (6PGDH, EC 1.1.1.44) and glucose 6-phosphate dehydrogenase (G6PDH, EC 1.1.1.49) from alfalfa (Medicago sativa L.). These exhibit extensive nucleotide and amino acid sequence similarity to the corresponding genes from bacteria, Drosophila and mammals. Transcripts encoding both enzymes are expressed at high levels in roots and nodules. Exposure of alfalfa suspension cells to an elicitor from yeast cell walls results in co-ordinated increases in transcription rates for both genes, followed by increased steady state transcript levels but only slightly increased extractable enzyme activities, at the onset of accumulation of isoflavonoid phytoalexins. Levels of NADPH and NADP remain relatively constant in alfalfa cells following elicitation. The rapid transcriptional activation of 6PGDH and G6PDH does not therefore appear to be a response to altered pyridine nucleotide redox state. These genes appear to respond to early events in elicitor-mediated signalling rather than to subsequent elicitor-induced changes in secondary metabolism. Hydrogen peroxide, a potential signal for elicitation of anti-oxidative genes in biologically stressed plant cells, did not induce 6PGDH or G6PDH transcripts or enzymatic activity.
我们从紫花苜蓿(Medicago sativa L.)中分离出了编码磷酸戊糖途径酶6-磷酸葡萄糖酸脱氢酶(6PGDH,EC 1.1.1.44)和葡萄糖6-磷酸脱氢酶(G6PDH,EC 1.1.1.49)的cDNA克隆。这些克隆与来自细菌、果蝇和哺乳动物的相应基因表现出广泛的核苷酸和氨基酸序列相似性。编码这两种酶的转录本在根和根瘤中高水平表达。将紫花苜蓿悬浮细胞暴露于酵母细胞壁激发子下,会导致这两个基因的转录速率协同增加,随后稳态转录本水平升高,但在异黄酮植保素积累开始时,可提取的酶活性仅略有增加。激发后,紫花苜蓿细胞中的NADPH和NADP水平保持相对恒定。因此,6PGDH和G6PDH的快速转录激活似乎不是对吡啶核苷酸氧化还原状态改变的反应。这些基因似乎对激发子介导的信号传导早期事件有反应,而不是对随后激发子诱导的次生代谢变化有反应。过氧化氢是生物胁迫植物细胞中诱导抗氧化基因的潜在信号,但它不会诱导6PGDH或G6PDH转录本或酶活性。