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《Chinese Journal of Antibiotics》 1991-01
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A STUDY OF NEW CLAVAM ANTIBIOTICS G0069

Zhang Wei-xi, Qi Chang-jing, Tian Tie, Xie Mei-yu,Chen Wen-jun and Sun Jing- jing (Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences, Beijing 100050)  
Three antibiotics, designated as G0069 A, B and C, were isolated from a strain of Streptomyces hygroscoptcus G0069, in 1983. The strain -was isolated from a soil sample collected in Xishuang banna, a subtropic region in Guangxi Zhuang Nationality Autonomous Region, China. The fermentation, isolation and purification of these antibiotics was reported. Based on the results of mass spectrum, 1H- and 13C-NMR spectra, IR, UV and amino acid analysis, antibiotics G0069 A, B and C were identified to be the clavam antibiotics. Antibiotics G0069 A and C, having a clavam skeleton each, with a serine·valine or a serine · alanine side chain respectively, were considered to be two new clavam antibiotics. The major component G0069 A was studied in detail. Antibiotic G0069 A has weak inhibitory effect against some yeasts and filamentous fungi, but has no antibacterial activity, even with some other βb-lactam antibictics in combination. Antibiotic G0069 A displayed negative results in the concentrations from 62,5μg/ml to l,000μg/ml tested in spermatogonial assay, and exhibited toxic effect at 1,000Mg/ml. But it showed strong growth inhibitory effect on KB cells.On the contrary, other β-lacturu antibiotics showed negative results. The action of antibiotic G0069 A on KB cells was assumed as the compound of the time-dependent type. Forteen culture cell lines were further used to test the growth inhibitory effects of G0069 A. It showed that antibiotic G0069 A has stronger efficacies (ED60 0.1μg/ml) against human neoplastic cell lines derived from solid cancer than the neoplastic cells originated from mouse or rat. But it showed no increase of the life span of BDF1 mice inoculated with p388 leukemia cells in any administration schedules. The negative results of in vivo test might be correlated to the combination of G006.9 A with rat serum protein.
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