Greenberg-Ofrath N, Terespolosky Y, Kahane I, Bar R
Department of Membrane and Ultrastructure Research, Hebrew University, Jerusalem, Israel.
Appl Environ Microbiol. 1993 Feb;59(2):547-51. doi: 10.1128/aem.59.2.547-551.1993.
The design of fully or partly defined media for mycoplasma cultivation involves the need to provide the essential lipids, cholesterol and long-chain fatty acids, in an assimilable and nontoxic form. This study introduces cyclodextrins (CDs) as carriers of these lipids, thus suggesting alternatives to serum or bovine serum albumin (BSA). The effects of beta-CD and two forms of chemically modified beta-CD, dimethyl-beta-CD (Dimeb) and hydroxypropyl-beta-CD (Hyprob), on the growth of Mycoplasma capricolum and Acholeplasma laidlawii were investigated in a basal medium as well as in serum- and BSA-supplemented media. beta-CD was found to inhibit the growth of the sterol-requiring M. capricolum in both serum and BSA media, but it stimulated the growth of the sterol-independent A. laidlawii. Inhibition by beta-CD was explained by its capacity to form a water-insoluble CD-cholesterol complex, thus rendering it unavailable to the cells. Dimeb, despite its strong complexing ability for lipids, was found to be toxic to all mycoplasma species in both liquid cultures and agar diffusion susceptibility tests. In sharp contrast to beta-CD and Dimeb, Hyprob (with a degree of substitution of 4.2) added at 5 and 10 mM to a basal medium supplemented with lipids permitted growth of M. capricolum. Comparison of growth curves in the two conventional serum and BSA media with those in two Hyprob media revealed comparable growth and growth rates.
用于支原体培养的完全或部分限定培养基的设计需要以可同化且无毒的形式提供必需的脂质、胆固醇和长链脂肪酸。本研究引入环糊精(CDs)作为这些脂质的载体,从而提出了血清或牛血清白蛋白(BSA)的替代物。在基础培养基以及补充了血清和BSA的培养基中,研究了β-环糊精以及两种化学修饰形式的β-环糊精,即二甲基-β-环糊精(Dimeb)和羟丙基-β-环糊精(Hyprob)对山羊支原体和莱氏无胆甾原体生长的影响。发现β-环糊精在血清和BSA培养基中均抑制需要甾醇的山羊支原体的生长,但它刺激了不依赖甾醇的莱氏无胆甾原体的生长。β-环糊精的抑制作用是由于其形成水不溶性环糊精-胆固醇复合物的能力,从而使细胞无法利用胆固醇。尽管Dimeb对脂质具有很强的络合能力,但发现在液体培养和琼脂扩散敏感性试验中,它对所有支原体物种均有毒性。与β-环糊精和Dimeb形成鲜明对比的是,在添加了脂质的基础培养基中添加5 mM和10 mM的Hyprob(取代度为4.2)可使山羊支原体生长。比较两种传统血清和BSA培养基与两种Hyprob培养基中的生长曲线,发现生长情况和生长速率相当。