Nagaoka K, Demain A L
J Antibiot (Tokyo). 1975 Sep;28(9):627-35. doi: 10.7164/antibiotics.28.627.
Microorganisms producing antibiotics have been genetically converted by earlier workers to mutants which cannot produce antibiotic without supplementation with a moiety of the antibiotic. These antibiotics include neomycin, kanamycin, paromomycin, butirosin, sisomicin, ribostamycin and novobiocin. Success has not been reported for organisms producing guanidinocyclitol antibiotics such as streptomycin. We mutagenized conidia of the streptomycin-producing Streptomyces griseus strain 7-455F3 with nitrosoguanidine at pH 7.0. Non-producers of streptomycin were visually selected by the agar-plug technique using Bacillus subtilis. We successfully isolated mutant MIT-A5 which produces no streptomycin unless streptidine is added to the agar medium. The streptidine-dependent phenotype was confirmed in submerged culture in flasks. Attempts to produce new antibiotics by feeding aminocyclitols to mutant MIT-A5 failed. However a new antibiotic (streptomutin A) was produced by supplementation with the guanidinocyclitol, 2-deoxystreptidine. We propose the term "mutational biosynthesis" for the production of new metabolites by the use of mutants blocked in the biosynthetic pathway to the secondary metabolite. We further propose the term "idiotroph" to properly describe such mutants.
早期的研究人员已将产生抗生素的微生物基因转化为突变体,这些突变体在不添加抗生素部分的情况下无法产生抗生素。这些抗生素包括新霉素、卡那霉素、巴龙霉素、丁胺卡那霉素、西索米星、核糖霉素和新生霉素。对于产生胍基环醇类抗生素(如链霉素)的微生物,尚未有成功的报道。我们用亚硝基胍在pH 7.0条件下诱变产生链霉素的灰色链霉菌菌株7-455F3的分生孢子。通过使用枯草芽孢杆菌的琼脂块技术,肉眼筛选出不产生链霉素的菌株。我们成功分离出突变体MIT-A5,该突变体除非在琼脂培养基中添加链霉胍,否则不产生链霉素。在摇瓶中的深层培养中证实了链霉胍依赖性表型。通过向突变体MIT-A5添加氨基环醇来生产新抗生素的尝试失败了。然而,通过添加胍基环醇2-脱氧链霉胍产生了一种新抗生素(链霉素A)。我们提出“突变生物合成”这一术语,用于描述通过利用在次生代谢物生物合成途径中受阻的突变体来生产新代谢物的过程。我们进一步提出“专性营养突变体”这一术语来恰当地描述此类突变体。