Pettit G R, Pettit G R, Backhaus R A, Boettner F E
Department of Chemistry, Arizona State University, Tempe 85287-1604.
J Nat Prod. 1995 Jan;58(1):37-43. doi: 10.1021/np50115a004.
By cloning Hymenocallis littoralis, a practical biosynthetic procedure was developed for producing pancratistatin [1]. The plant tissue culture-->greenhouse-->field production sequence was successively utilized for increasing an original 1.5 kg of wild H. littoralis bulbs to some 60,000 bulbs at present. In the central Arizona Sonoran Desert, the tropical H. littoralis was found to reach a maximum pancratistatin content in October and a minimum in May. Generally pancratistatin [1] was accompanied by lesser yields of narciclasine [2], 7-deoxynarciclasine [3], and 7-deoxy-trans-dihydronarcicasine [4]. Improved laboratory and pilot-plant scale techniques were also developed for the isolation of pancratistatin [1] from difficult-to-separate mixtures of narciclasine [2] and 7-deoxynarciclasine [3]occurring in H. littoralis.
通过克隆海滨蜘蛛兰,开发了一种用于生产 pancratistatin 的实用生物合成程序[1]。依次利用植物组织培养→温室→田间生产流程,将最初 1.5 千克野生海滨蜘蛛兰鳞茎增加到目前约 60000 个鳞茎。在亚利桑那州中部的索诺兰沙漠,发现热带海滨蜘蛛兰的 pancratistatin 含量在 10 月达到最高,5 月达到最低。一般来说,pancratistatin[1]伴随着较低产量的水仙环素[2]、7-脱氧水仙环素[3]和 7-脱氧反式二氢水仙环素[4]。还开发了改进的实验室和中试规模技术,用于从海滨蜘蛛兰中难以分离的水仙环素[2]和 7-脱氧水仙环素[3]混合物中分离出 pancratistatin[1]。