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L-[αS, 5S]-α-氨基-3-氯-4,5-二氢-5-异恶唑乙酸(NSC-163501):一种具有L-谷氨酰胺拮抗剂特性的新型氨基酸抗生素。

L-[alphaS, 5S]-alpha-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (NSC-163501): a new amino acid antibiotic with the properties of an antagonist of L-glutamine.

作者信息

Jayaram H N, Cooney D A, Ryan J A, Neil G, Dion R L, Bono V H

出版信息

Cancer Chemother Rep. 1975 May-Jun;59(3):481-91.

PMID:1147
Abstract

L-[alphaS,5S]-alpha-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (NSC-163501), an antibiotic elaborated by Streptomyces sviceus, has been shown to be a powerful inhibitor of many mammalian and bacterial reactions involving the transfer of nitrogen from the gamma-carboxamide of L-glutamine. Thus, the utilization of L-glutamine for the synthesis of carbamyl phosphate, L-asparagine, guanosine-5'-monophosphate, cytidine-5'-triphosphate, N-formylglycinamidine ribonucleotide, NAD, glucosamine-6-phosphate, and anthranilic acid is strongly or totally inhibited by a concentration of NSC-163501 of 1 X 10(-3) M. L-Glutamate synthetase of Escherichia coli is only modestly inhibited and 5-phosphoribosylamine synthesis in fetal rat liver is comparatively refractory to inhibition. NSC-163501 treatment of L1210 cells growing in a low L-glutamine culture medium produced arrest in G or early S phase. Of the amino acids tested, only L-glutamine antagonized such growth inhibition.

摘要

L-[-αS,5S]-α-氨基-3-氯-4,5-二氢-5-异恶唑乙酸(NSC-163501)是一种由灰色链霉菌产生的抗生素,已被证明是许多涉及从L-谷氨酰胺的γ-羧酰胺转移氮的哺乳动物和细菌反应的强力抑制剂。因此,1×10⁻³ M浓度的NSC-163501能强烈或完全抑制利用L-谷氨酰胺合成氨甲酰磷酸、L-天冬酰胺、鸟苷-5'-单磷酸、胞苷-5'-三磷酸、N-甲酰甘氨脒核糖核苷酸、NAD、6-磷酸葡糖胺和邻氨基苯甲酸。大肠杆菌的L-谷氨酸合成酶仅受到适度抑制,而胎鼠肝脏中的5-磷酸核糖胺合成相对不易受到抑制。用NSC-163501处理在低L-谷氨酰胺培养基中生长的L1210细胞会导致细胞停滞在G期或早期S期。在测试的氨基酸中,只有L-谷氨酰胺能拮抗这种生长抑制。

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