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生长培养基对大肠杆菌细胞组成及头孢他啶敏感性的影响

Influence of growth media on Escherichia coli cell composition and ceftazidime susceptibility.

作者信息

Malouin F, Chamberland S, Brochu N, Parr T R

机构信息

Laboratoire et Service d'Infectiologie, Université Laval, Quebec, Canada.

出版信息

Antimicrob Agents Chemother. 1991 Mar;35(3):477-83. doi: 10.1128/AAC.35.3.477.

Abstract

Cell composition and surface properties of Escherichia coli were modified by using various growth media to investigate the role of yet uncharacterized components in ceftazidime susceptibility. An eightfold dilution of Luria broth was used as the basic growth medium and was supplemented with up to 4% phosphate, 5% glucose, or 12% L-glutamate. Decreases in cephaloridine and ceftazidime susceptibility, of two- and eightfold, respectively, were observed only in the glucose-enriched medium. The outer membrane permeability to ceftazidime and cephaloridine was evaluated by crypticity indices. Indices were unchanged under all growth conditions. Fluorometry of whole cells with 1-N-phenylnaphthylamine showed that glucose does not affect the interaction of this hydrophobic probe with the membranes but showed that elevated concentrations of phosphate or glutamate cause a marked increase in cell hydrophobicity, which, in turn, correlates with an increase in the susceptibility of E. coli to nalidixic acid. Growth in phosphate- or glutamate-enriched media caused an augmentation in major phospholipid species and may explain the increased hydrophobicity and susceptibility of E. coli to nalidixic acid. These data showed that E. coli susceptibility to ceftazidime is not influenced by cell surface hydrophobicity and suggested that the contribution of a nonspecific lipophilic diffusion route for entry of ceftazidime into cells is not likely to occur or is distinct from that of more hydrophobic molecules such as nalidixic acid. Finally, the penicillin-binding proteins of the E. coli cells were also investigated. Penicillin-binding protein 8 was only markedly labeled with 125I-penicillin V in inner membranes extracted from cells grown with glucose. Results of this study suggest that the unexpected change in penicillin-binding protein 8 observed in the presence of glucose may be responsible for the increase in MICs of cephaloridine and ceftazidime.

摘要

通过使用各种生长培养基来修饰大肠杆菌的细胞组成和表面性质,以研究尚未明确的成分在头孢他啶敏感性中的作用。将八倍稀释的Luria肉汤用作基本生长培养基,并补充高达4%的磷酸盐、5%的葡萄糖或12%的L-谷氨酸。仅在富含葡萄糖的培养基中观察到头孢菌素和头孢他啶敏感性分别降低了两倍和八倍。通过隐蔽性指数评估外膜对头孢他啶和头孢菌素的通透性。在所有生长条件下,指数均未改变。用1-N-苯基萘胺对全细胞进行荧光测定表明,葡萄糖不影响这种疏水探针与膜的相互作用,但表明磷酸盐或谷氨酸浓度升高会导致细胞疏水性显著增加,这反过来又与大肠杆菌对萘啶酸敏感性的增加相关。在富含磷酸盐或谷氨酸的培养基中生长会导致主要磷脂种类增加,这可能解释了大肠杆菌对萘啶酸疏水性和敏感性的增加。这些数据表明,大肠杆菌对头孢他啶的敏感性不受细胞表面疏水性的影响,并表明头孢他啶进入细胞的非特异性亲脂性扩散途径的作用不太可能发生,或者与萘啶酸等疏水性更强的分子不同。最后,还研究了大肠杆菌细胞的青霉素结合蛋白。仅在用葡萄糖培养的细胞提取的内膜中,青霉素结合蛋白8被125I-青霉素V显著标记。本研究结果表明,在葡萄糖存在下观察到的青霉素结合蛋白8的意外变化可能是头孢菌素和头孢他啶最低抑菌浓度增加的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a98b/245035/d613b17e2b37/aac00048-0125-a.jpg

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