EFFECTS OF BETA-LACTAM ANTIBIOTICS ON PEPTIDOGLYCAN SYNTHESIS IN GROWING NEISSERIA-GONORRHOEAE, INCLUDING CHANGES IN THE DEGREE OF O-ACETYLATION
EFFECTS OF BETA-LACTAM ANTIBIOTICS ON PEPTIDOGLYCAN SYNTHESIS IN GROWING NEISSERIA-GONORRHOEAE, INCLUDING CHANGES IN THE DEGREE OF O-ACETYLATION
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DOI:
10.1128/jb.147.2.633-641.1981
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发表时间:
1981-01-01
影响因子:
3.2
通讯作者:
PERKINS, HR
中科院分区:
文献类型:
--
作者:
BLUNDELL, JK;PERKINS, HR
Low concentrations of .beta.-lactam antibiotics caused an increased uptake of radioactive glucosamine into the sodium dodecyl sulfate[SDS]-insoluble peptidoglycan of growing N. gonorrhoeae. There was no appreciable change in the (small) amount of SDS-soluble polymer present in the cultures. The SDS-insoluble product in control cells was only partially dissolved by egg white lysozyme (about 40%) but could all be released by the Chalaropsis B muramidase. In cells exposed to .beta.-lactams the proportion of labeled peptidoglycan susceptible to lysozyme increased to 60%. Examination of the Chalaropsis B digests by TLC showed that they contained disaccharide-peptide monomers with and without O-acetylation and bis-disaccharide-peptide dimers with 1 or 2 O-acetyl groups or with none. .beta.-Lactam antibiotics caused a decrease in the degree of O-acetylation but did not greatly affect the amount of peptidoglycan cross-linking. They also had the effect of enlarging the bacteria and conserving and thickening the septa that could be observed in thin sections under the EM. The relationship between these results and the effects of .beta.-lactams on in vitro synthesis of peptidoglycan by ether-treated N. gonorrhoeae is discussed.