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Pycnial nectar of rust fungi induces cap formation on pycniospores of opposite mating type

机译:锈菌的碧萝n花蜜在相反交配型的碧萝ios上诱导帽形成

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Pycnial nectar (including pycniospores) transferred between pycnia of opposite mating type (as indicated by subsequent aecium formation) induced formation of a cap on one end of pycniospores. The polar caps developed with seven species of Puccinia and four of Uromyces, but not with P. helianthi, Tranzschelia pruni-spinosae, or U. vignae. Caps were induced equally in reciprocal transfers of nectar between pycnia of opposite mating type. The caps stained with India ink, or labeled with colloidal gold or wheat germ agglutinin conjugated with fluorescein isothiocyanate (WGA-FITC), but were not visible in unstained preparations. Cap formation started within 10 min of nectar transfer and was completed in 20-60 min. Nectar retained cap-inducing activity after pycniospores were removed by centrifugation, whereas pycniospores washed free of nectar did not induce caps. Pycniospores that were removed from a pycnium and induced to form caps by pycniospore-free nectar of opposite mating type did not induce aecia when returned to the original pycnium, showing that cap formation alone was not sufficient for completion of mating processes. Caps were removed by treatment with proteinase K, sodium dodecyl sulfate (SDS), or 0.01 N HCl, indicating the presence of protein. Labeling by WGA-FITC suggested the presence of polysaccharides or glycoproteins containing N-acetylglucosamine. The cap-inducing activity of nectar was lost if the nectar was boiled or autoclaved. Cap-inducing nectar contained a complex of high molecular weight proteins larger than 100 kDa as shown by native polyacrylamide gel electrophoresis analysis. This protein complex had cap-inducing activity as determined by placing pycniospores directly on gels after electrophoresis. In SDS gels, 6-7 polypeptides ranging in size from 14-70 kDa were observed, but bioassays of these polypeptides for cap induction were negative. The results indicate that pycnial nectar of several rust species contains high molecular weight cap-inducing proteins which are mating type-specific and induce pycniospore cap formation as an early event associated with processes leading to fertilization.
机译:在相反交配类型的脓疱之间转移的脓疱花蜜(包括脓孢子)(如随后的ec形成)表明,在孢子的一端形成了顶盖。极帽的发育有七个物种的Puccinia和四个Uromyces,但没有发育到P. helianthi,Transschelia pruni-spinosae或U. vignae。在相反交配类型的脓菌之间,在花蜜的相互转移中均诱导了帽。瓶盖用印度墨水染色,或用与异硫氰酸荧光素(WGA-FITC)共轭的胶体金或小麦胚芽凝集素标记,但在未染色的制剂中不可见。在花蜜转移后的10分钟内开始盖形成,并在20-60分钟内完成。通过离心除去孢子孢子后,花蜜保留了诱导帽的活性,而从花蜜中洗去的孢子却没有诱导帽。从交配子上移除的交配孢子并被相反交配类型的无交配孢子的花蜜诱导形成瓶盖的孢子在返回到原始的分生孢子时并没有引起盲肠,这表明仅形成瓶盖不足以完成交配过程。通过用蛋白酶K,十二烷基硫酸钠(SDS)或0.01 N HCl处理除去盖子,表明存在蛋白质。 WGA-FITC标记表明存在含有N-乙酰氨基葡萄糖的多糖或糖蛋白。如果将花蜜煮沸或高压灭菌,则会丧失诱导花蜜的帽的活性。如天然聚丙烯酰胺凝胶电泳分析所示,诱导帽的花蜜含有大于100 kDa的高分子量蛋白质复合物。该蛋白复合物具有帽诱导活性,如通过在电泳后将芽孢子孢子直接置于凝胶上所测定的。在SDS凝胶中,观察到6-7个多肽,大小从14-70 kDa不等,但是这些多肽用于帽诱导的生物测定结果是阴性的。结果表明,几种锈菌种的瓶状花蜜都含有高分子量的帽盖诱导蛋白,这些蛋白是交配型特异性的,并诱导了瓶盖孢子帽形成,这是导致受精过程的早期事件。

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