Friedrich C G, Demain A L
Appl Environ Microbiol. 1977 Dec;34(6):706-9. doi: 10.1128/aem.34.6.706-709.1977.
Compounds structurally related to lysine were tested against Penicillium chrysogenum Wis. 54-1255 for inhibition of growth, sporulation, and penicillin formation. This strain is relatively resistant to lysine analogs. The compounds that were the more active inhibitors of growth and whose activities were reversed by L-lysine were diaminohexynoic acid, N-epsilon-methyllysine, N-alpha-methyllysine, and diaminopimelic acid. These four compounds also inhibited sporulation, which was more sensitive to inhibition than growth was. Analogs strongly inhibiting benzyl-penicillin formation by resting mycelia were diaminohexynoic acid and N-epsilon-methyllysine. The action of the most active analog (diaminohexynoic acid) on penicillin synthesis was reversed by DL-alpha-aminoadipic acid.
测试了与赖氨酸结构相关的化合物对产黄青霉Wis. 54 - 1255生长、孢子形成和青霉素合成的抑制作用。该菌株对赖氨酸类似物相对耐药。对生长抑制活性更强且其活性可被L - 赖氨酸逆转的化合物有二氨基己炔酸、N - ε - 甲基赖氨酸、N - α - 甲基赖氨酸和二氨基庚二酸。这四种化合物也抑制孢子形成,孢子形成比生长对抑制更敏感。强烈抑制静止菌丝体合成苄青霉素的类似物是二氨基己炔酸和N - ε - 甲基赖氨酸。活性最强的类似物(二氨基己炔酸)对青霉素合成的作用可被DL - α - 氨基己二酸逆转。