Masurekar P S, Fountoulakis J M, Hallada T C, Sosa M S, Kaplan L
Merck Research Laboratories, Merck and Co. Inc., Rahway, NJ 07065-0900.
J Antibiot (Tokyo). 1992 Dec;45(12):1867-74. doi: 10.7164/antibiotics.45.1867.
Zalerion arboricola ATCC 20868 produces pneumocandin A0 (L-671,329), a cyclic hexapeptide with a dimethylmyristic acid side chain. This compound has anti-candida and anti-pneumocystis activities. We were interested in looking for other related compounds produced by this organism. To facilitate this search, a simple medium (S2) composed of D-mannitol, peptonized milk, lactic acid, glycine, KH2PO4 and trace elements, which supported the production of a number of such compounds, was designed. For the isolation of mutants, either spores or growing mycelia were treated with N-nitroso-N-methylurethane or N-methyl-N'-nitro-N-nitrosoguanidine and survivors were screened for changes in the product spectrum. From approximately 1,500 survivors tested, 5 mutants were isolated. Mutants ATCC 20957, 74030, 20958 and 20988 exclusively produce various pneumocandins other than A0. These compounds were active against Candida and Pneumocystis carinii. The yield of A0 was found to be increased 2.5-fold over that of the parent in the fifth mutant, MF5415. Further medium studies indicated that the addition of soybean oil to S2 medium improved the yields. Subsequent development of another series of media containing Pharmamedia as a nitrogen source resulted in increase in production by 10- approximately 20-fold. Overall, these studies resulted in substantial improvement in the production of A0 as well as discovery and/or facile production of 7 other related compounds.
树状枝孢菌ATCC 20868能产生肺炎菌素A0(L-671,329),这是一种带有二甲基肉豆蔻酸侧链的环状六肽。该化合物具有抗念珠菌和抗肺孢子菌活性。我们对寻找该菌株产生的其他相关化合物感兴趣。为便于此项研究,设计了一种由D-甘露醇、胨化乳、乳酸、甘氨酸、KH2PO4和微量元素组成的简单培养基(S2),该培养基能支持多种此类化合物的产生。为分离突变体,用N-亚硝基-N-甲基脲或N-甲基-N'-硝基-N-亚硝基胍处理孢子或生长中的菌丝体,并筛选存活菌株的产物谱变化。在测试的约1500个存活菌株中,分离出5个突变体。突变体ATCC 20957、74030、20958和20988只产生除A0之外的各种肺炎菌素。这些化合物对念珠菌和卡氏肺孢子菌有活性。在第五个突变体MF5415中,发现A0的产量比亲本提高了2.5倍。进一步的培养基研究表明,向S2培养基中添加大豆油可提高产量。随后开发的另一系列以Pharmamedia作为氮源的培养基使产量提高了10至约20倍。总体而言,这些研究使A0的产量大幅提高,同时发现和/或轻松生产了其他7种相关化合物。