Bacon C W
Toxicology & Mycotoxins Research Unit, U.S. Department of Agriculture, Athens, Georgia 30613.
Appl Environ Microbiol. 1988 Nov;54(11):2615-8. doi: 10.1128/aem.54.11.2615-2618.1988.
A procedure was developed to isolate and determine ergot alkaloid production by Acremonium coenophialum, the endophytic fungus of tall fescue. The procedure established that macerated leaf sheath or pith from inflorescence stem placed either in a liquid medium or on a corn meal-malt extract agar medium produced isolated mycelium and characteristic conidia within a 3- to 3.5-week period. Once isolated, each fungus was placed in another liquid medium, M104T, where competent strains produced total ergot alkaloids ranging from 38 to 797 mg/liter. Several isolates were negative for ergot alkaloid synthesis. The production of ergot alkaloids by individual isolates was unstable; isolates rapidly degenerated in their ability to produce ergot alkaloids during subculture. However, the procedure as presented allows the assessment of an isolate for ergot alkaloid synthesis during its initial isolation.
开发了一种用于分离和测定高羊茅内生真菌——共生顶孢霉产生麦角生物碱的方法。该方法确定,将来自花序茎的浸软叶鞘或髓置于液体培养基或玉米粉-麦芽提取物琼脂培养基中,在3至3.5周内可产生分离的菌丝体和特征性分生孢子。一旦分离出来,将每种真菌置于另一种液体培养基M104T中,有能力的菌株产生的总麦角生物碱范围为38至797毫克/升。有几种分离株麦角生物碱合成呈阴性。单个分离株产生麦角生物碱的情况不稳定;在继代培养过程中,分离株产生麦角生物碱的能力迅速退化。然而,所介绍的方法允许在最初分离期间评估分离株的麦角生物碱合成情况。