Pinkerton F, Strobel G
Department of Plant Pathology, Montana State University, Bozeman, Mont. 59715.
Proc Natl Acad Sci U S A. 1976 Nov;73(11):4007-11. doi: 10.1073/pnas.73.11.4007.
Successive transfer in synthetic medium of spores and mycelial fragments from original toxin-producing cultures of Helminthosporium sacchari results in attenuated cultures which do not produce the host-specific toxin helminthosporoside. When attenuated cultures are grown on material obtained from the water wash of sugarcane leaves susceptible to this fungus, the production of heminthosporoside resumes. Compounds that activate toxin production in the fungus are present on the leaf surface and presumably arise via plant metabolism. One activator was identified as a novel free amine, serinol (2-amino-1,3-propanediol). It activates toxin production in attenuated cultures at 1 muM. Several experiments described in this report argue against the selection theory for the attenuation of cultures. The biological significance and some possible mechanisms for the activation of toxin biosynthesis are discussed.
将来自甘蔗长蠕孢菌原始产毒素培养物的孢子和菌丝体片段在合成培养基中连续传代,会产生减毒培养物,这些培养物不再产生宿主特异性毒素甘蔗长蠕孢菌素。当减毒培养物在从易受这种真菌侵染的甘蔗叶水洗物中获得的材料上生长时,甘蔗长蠕孢菌素的产生又会恢复。激活真菌毒素产生的化合物存在于叶片表面,推测是通过植物代谢产生的。一种激活剂被鉴定为一种新型游离胺,丝氨醇(2-氨基-1,3-丙二醇)。它在1μM浓度下可激活减毒培养物中的毒素产生。本报告中描述的几个实验反驳了培养物减毒的选择理论。讨论了毒素生物合成激活的生物学意义和一些可能机制。