Ugalde U O, Virto M D, Pitt D
Departamento de Quimica Aplicada, Universidad del Pais Vasco, San Sebastian, Spain.
Antonie Van Leeuwenhoek. 1990 Jan;57(1):43-9. doi: 10.1007/BF00400335.
Cell wall-free protoplasts of P. cyclopium could regenerate a cell wall and form mycelia in liquid culture with high rates of viability. When calcium was added to the medium, protoplasts displayed biphasic accumulation with an immediate metabolism-independent adsorption phase, followed by slow metabolism-dependent uptake. Exposure of the protoplasts to Ca2+ for periods of 2 min, followed by incubation in calcium-free medium for 24 hours, was sufficient to induce conidiation with morphogenetic events parallel to those found in cultures containing calcium throughout the incubation period, and similar to those reported in cultures inoculated from conidia. The conidiation event caused by short exposure to calcium could be reversed, within 2 hours of Ca2+ addition, by a brief treatment with the specific calcium chelating agent BAPTA (100 microM), which removed 65 to 75% of the total cell calcium. The results implicate the membrane-bound calcium fraction in the process of conidiation induction.
环纹梨孢菌的无细胞壁原生质体能够再生细胞壁,并在液体培养中形成菌丝体,且具有较高的活力。当向培养基中添加钙时,原生质体呈现双相积累,先是一个与代谢无关的快速吸附阶段,随后是缓慢的依赖代谢的摄取阶段。将原生质体暴露于Ca2+ 2分钟,然后在无钙培养基中孵育24小时,足以诱导产孢,其形态发生事件与在整个孵育期含钙培养物中发现的事件平行,且与从分生孢子接种的培养物中报道的事件相似。短时间暴露于钙引起的产孢事件,在添加Ca2+后2小时内,可通过用特定的钙螯合剂BAPTA(100微摩尔)进行短暂处理而逆转,该处理去除了总细胞钙的65%至75%。结果表明膜结合钙组分参与了产孢诱导过程。