School of Botany, The University of Melbourne, Victoria 3010 Australia.
Mol Plant Pathol. 2007 Nov;8(6):791-802. doi: 10.1111/j.1364-3703.2007.00433.x.
SUMMARY Sirodesmin PL is a non-host-selective phytotoxin produced by Leptosphaeria maculans, which causes blackleg disease of canola (Brassica napus). Previous studies have shown that sirodesmin PL biosynthesis involves a cluster of 18 co-regulated genes and that disruption of the two-module non-ribosomal peptide synthetase gene (sirP) in this cluster prevents the production of sirodesmin PL. Loss of sirodesmin PL did not affect the growth or fertility of the sirP mutant in vitro, but this mutant had less antibacterial and antifungal activity than the wild-type. When the sirP mutant was inoculated on to cotyledons of B. napus, it caused similar-sized lesions on cotyledons as the wild-type isolate, but subsequently caused fewer lesions and was half as effective as the wild-type in colonizing stems, as shown by quantitative PCR analyses. However, no significant difference was observed in size of lesions when either wild-type or mutant isolates were injected directly into the stem. The expression of two cluster genes, sirP and an ABC transporter, sirA, was studied in planta. Fungal isolates containing fusions of the green fluorescent protein gene with the promoters of these genes fluoresced after 10 days post-inoculation (dpi). Transcripts of sirP and sirA were detected after 11 dpi in cotyledons by reverse transcriptase PCR, and expression of both genes increased dramatically in stem tissue. This expression pattern was consistent with the distribution of sirodesmin PL in planta as revealed by mass spectrometry experiments.
摘要 丝氨酸 PL 是菜黑粉菌产生的一种非宿主选择性植物毒素,可引起油菜黑胫病。先前的研究表明,丝氨酸 PL 的生物合成涉及一个由 18 个共同调节基因组成的簇,而该簇中的两个模块非核糖体肽合酶基因(sirP)的破坏阻止了丝氨酸 PL 的产生。在体外,丝氨酸 PL 的缺失并不影响 sirP 突变体的生长或育性,但与野生型相比,该突变体的抗菌和抗真菌活性较低。当 sirP 突变体接种到油菜子叶上时,它在子叶上引起的病变与野生型分离株相似,但随后引起的病变较少,在定殖茎部方面的效果是野生型的一半,这通过定量 PCR 分析得到证实。然而,当直接将野生型或突变型分离物注入茎部时,病变的大小没有明显差异。研究了两种簇基因 sirP 和 ABC 转运蛋白 sirA 在体内的表达。含有这些基因启动子与绿色荧光蛋白基因融合的真菌分离物在接种后 10 天(dpi)开始发出荧光。反转录 PCR 检测到 11 dpi 时在子叶中检测到 sirP 和 sirA 的转录本,并且这两个基因在茎组织中的表达显著增加。这种表达模式与质谱实验揭示的丝氨酸 PL 在体内的分布一致。