Department of Plant Pathology, University of California, Davis, CA 95616-8680, USA.
Fungal Genet Biol. 2013 Feb;51:72-83. doi: 10.1016/j.fgb.2012.11.007. Epub 2012 Dec 1.
Gamma-glutamyltransferase (GGT, EC 2.3.2.2) cleaves the γ-glutamyl linkage in glutathione (GSH). Three GGTs in the hemibiotrophic plant pathogen Colletotrichum graminicola were identified in silico. GGT mRNA expression was monitored by quantitative reverse-transcriptase PCR. Expression of all three genes was detected in planta during the biotrophic and necrotrophic stages of infection. Of the three GGTs, CgGGT1 mRNA (from gene GLRG_09590) was the most highly expressed. All three GGT mRNAs were up-regulated in wild type nitrogen-starved germlings in comparison to non-starved germlings. CgGGT1 was insertionally mutagenized in C. graminicola, complemented with the wild type form of the gene, and over-expressed. Enzyme assays of two independent CgGGT1 knockouts and the wild type indicated that CgGGT1 is the major GGT and accounts for 86% and 68% of total GGT activity in conidia and mycelia, respectively. The over-expressing strain had 8-fold and 3-fold more enzyme activity in conidia and mycelia, respectively, than the wild type. In an analysis of the GGT knockout, complemented and over-expressing strains, GGT1 transcript levels are highly correlated (r=0.95) with levels of total GGT enzyme activity. CgGGT1 and CgGGT2 genes in strains that had ectopic copies of CgGGT1 were not up-regulated by nitrogen-starvation, in contrast to the wild type. Deletion or over-expression of CgGGT1 had no effect on mRNA expression of CgGGT2 and CgGGT3. In broth in which 3 and 6mM glutathione (GSH) was the nitrogen source, the CgGGT1 over-expressing strain produced significantly (P<0.0001) more biomass than the wild type and complemented strains, whereas the CgGGT1Δ strains produced significantly (P<0.0001) less biomass than the wild type strain. This suggests that CgGGT1 is involved in utilizing GSH as a nitrogen source. However, deletion and over-expression of CgGGT1 had no effect on either virulence in wounded corn leaf sheaths or GSH levels in conidia and mycelia. Thus, the regulation of GSH concentration is apparently independent of CgGGT1 activity.
γ-谷氨酰转移酶(GGT,EC 2.3.2.2)可切割谷胱甘肽(GSH)中的γ-谷氨酰键。在半活体植物病原体炭疽菌中,通过计算机从生物信息学上鉴定了三种 GGT。通过定量逆转录-PCR 监测 GGT mRNA 的表达。在感染的生物亲和和坏死阶段,所有三种基因均在植物中被检测到。在三种 GGT 中,CgGGT1 mRNA(来自基因 GLRG_09590)的表达量最高。与非饥饿的芽生菌相比,所有三种 GGT mRNA 在野生型氮饥饿芽生菌中均上调。CgGGT1 在炭疽菌中被插入突变,用该基因的野生型进行互补,并过表达。对两个独立的 CgGGT1 敲除突变体和野生型的酶活性测定表明,CgGGT1 是主要的 GGT,分别占孢子和菌丝中总 GGT 活性的 86%和 68%。过表达菌株的孢子和菌丝中的酶活性分别比野生型高 8 倍和 3 倍。在对 GGT 敲除、互补和过表达菌株的分析中,GGT1 转录本水平与总 GGT 酶活性高度相关(r=0.95)。在具有 CgGGT1 异位拷贝的菌株中,CgGGT2 和 CgGGT3 基因不受氮饥饿的上调,与野生型形成对比。CgGGT1 的缺失或过表达对 CgGGT2 和 CgGGT3 的 mRNA 表达没有影响。在含有 3 和 6mM 谷胱甘肽(GSH)作为氮源的肉汤中,CgGGT1 过表达菌株的生物量明显(P<0.0001)高于野生型和互补菌株,而 CgGGT1Δ 菌株的生物量明显(P<0.0001)低于野生型菌株。这表明 CgGGT1 参与利用 GSH 作为氮源。然而,CgGGT1 的缺失和过表达对玉米叶片鞘受伤后的致病性或孢子和菌丝中的 GSH 水平均无影响。因此,GSH 浓度的调节显然与 CgGGT1 活性无关。