Multidisciplinary Institute for Environmental Studies (MIES) Ramón Margalef, Department of Marine Sciences and Applied Biology, University of Alicante, Aptdo. 99, 03080 Alicante, Spain.
Fungal Genet Biol. 2010 Apr;47(4):342-51. doi: 10.1016/j.fgb.2010.01.004. Epub 2010 Jan 25.
Nematophagous fungi Pochonia chlamydosporia and P. rubescens colonize endophytically barley roots. During nematode infection, serine proteases are secreted. We have investigated whether such proteases are also produced during root colonization. Polyclonal antibodies against serine protease P32 of P. rubescens cross-reacted with a related protease (VCP1) of P. chlamydosporia, but not with barley proteases. These antibodies also detected an unknown ca. 65-kDa protein, labeled hyphae and appressoria of P. chlamydosporia and strongly reduced proteolytic activity of extracts from fungus-colonized roots. Mass spectrometry (MS) of 32-kDa protein bands detected peptides homologous to VCP1 only in Pochonia-colonized roots. Peptides homologous to barley serine carboxypeptidases were found in 65kDa bands of all roots. RT-PCR detected expression of VCP1 and a new P. chlamydosporia serine carboxypeptidase (SCP1) genes only in fungus-colonized roots. SCP1 shared limited sequence homology with VCP1 and P32. Expression in roots of proteases from nematophagous fungi could be greatly relevant for nematode biocontrol.
食线虫真菌厚垣轮枝菌和玫烟色棒束孢定殖于大麦的根内。在感染线虫的过程中,会分泌丝氨酸蛋白酶。我们研究了在根定殖过程中是否也会产生这种蛋白酶。针对玫烟色棒束孢丝氨酸蛋白酶 P32 的多克隆抗体与亲缘关系密切的另一种蛋白酶(VCP1)发生交叉反应,但与大麦蛋白酶没有反应。这些抗体还检测到一种未知的约 65 kDa 蛋白,标记了厚垣轮枝孢的菌丝和附着胞,并强烈降低了定殖于根的真菌提取物的蛋白水解活性。对 32 kDa 蛋白条带的质谱(MS)分析仅在厚垣轮枝孢定殖的根中检测到与 VCP1 同源的肽。在所有根的 65 kDa 条带中都发现了与大麦丝氨酸羧肽酶同源的肽。RT-PCR 仅在真菌定殖的根中检测到 VCP1 和新的厚垣轮枝孢丝氨酸羧肽酶(SCP1)基因的表达。SCP1 与 VCP1 和 P32 仅有有限的序列同源性。食线虫真菌蛋白酶在根中的表达可能对线虫的生物防治有很大的相关性。