Hitchcock M J, Katz E
Antimicrob Agents Chemother. 1978 Jan;13(1):104-14. doi: 10.1128/AAC.13.1.104.
Conditions are described for the formation of protoplasts from Streptomyces parvulus that are able to synthesize actinomycin D de novo. Antibiotic synthesis by protoplasts, in contrast to that by mycelium, was sensitive to inhibition by actinomycin D and to a decrease in sucrose concentration. On the other hand, synthesis by mycelium was much more sensitive to inhibition by amino acid analogs (d-valine, cis-3-methylproline, and alpha-methyl-dl-tryptophan). In addition, the uptake of amino acids (l-methionine, sarcosine, and l- and d-valine) by protoplasts was significantly lower than that by mycelium. The advantages and limitations of using protoplasts for studying in vivo actinomycin synthesis are discussed.
描述了从小链霉菌形成原生质体的条件,这些原生质体能够从头合成放线菌素D。与菌丝体相比,原生质体的抗生素合成对放线菌素D的抑制和蔗糖浓度的降低敏感。另一方面,菌丝体的合成对氨基酸类似物(D-缬氨酸、顺式-3-甲基脯氨酸和α-甲基-DL-色氨酸)的抑制更为敏感。此外,原生质体对氨基酸(L-甲硫氨酸、肌氨酸以及L-和D-缬氨酸)的摄取明显低于菌丝体。讨论了使用原生质体研究体内放线菌素合成的优点和局限性。