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首页> 外文期刊>Journal of bacteriology >Release of Membrane Components from Viable Haemophilus parainfluenzae by Ethylenediaminetetraacetic Acid-Tris(hydroxymethyl)-aminomethane
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Release of Membrane Components from Viable Haemophilus parainfluenzae by Ethylenediaminetetraacetic Acid-Tris(hydroxymethyl)-aminomethane

机译:通过乙二胺四乙酸-TRIS(羟甲基) - 氨基甲烷从可行的血液硫脲慢性氟苯甲酸释放膜组分

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Logarithmically growing Haemophilus parainfluenzae lost 15 to 20% of the phospholipids, demethyl vitamin K2, cytochrome b, and cytochrome c, and 50% of the lipopolysaccharide when incubated in ethylenediaminetetraacetic acid (EDTA)-tris-(hydroxymethyl)aminomethane (Tris) for 10 min. This loss of membrane components occurred without loss in viability, and the lost components were recovered as membrane fragments in the surrounding buffer. The phospholipids recovered in the membrane fragments had a slightly lower specific activity than the phospholipids in the residue. Lysis of a portion of the cells could not account for the release of membrane components, as the cells lost neither glucose-6-phosphate dehydrogenase activity not deoxyribonucleic acid. The treated cells were osmotically stable and contained the same proportions of the individual phospholipids as pretreatment cells. Prolongation of the EDTA-Tris treatment did not induce further loss of phospholipid or demethyl vitamin K2, but caused a decrease in viability. If the cells were returned to the growth medium after 10 min, the cells immediately resumed growth at the pretreatment rate. During growth in the recovery period, the phospholipids increased logarithmically in the pretreatment rate. During growth in the recovery period, the phospholipids increased logarithmically in the pretreatment proportions, although there was a marked decrease in the turnover and a shift from the use of extracellular lipid precursors to the use of intracellular pools of precursors.
机译:对数生长血液血硫磺酸血红素损失15至20%的磷脂,去甲基维生素K 2 ,细胞色素 b ,和细胞色素 C 和50%的脂多糖。这种膜组分的损失发生在没有活力的情况下发生,并且将丢失的组分作为周围缓冲液中的膜片段回收。在膜片段中回收的磷脂具有比残余物中的磷脂略低的比活性。由于细胞缺损葡萄糖-6-磷酸脱氢酶活性而不是脱氧核糖核酸,因此一部分细胞的裂解无法解释膜组分的释放。处理过的细胞渗透稳定并含有与预处理细胞相同的单个磷脂的比例。 EDTA-TRIS治疗的延长没有诱导进一步荧光磷脂或去甲基维生素K 2 ,但导致活力降低。如果在10分钟后将细胞返回到生长培养基,则细胞立即在预处理率下恢复生长。在恢复期生长期间,磷脂以预处理率的对数增加。在恢复期的生长期间,磷脂在预处理比例中对数上增加,尽管周转数明显减少和从使用细胞外脂质前体与细胞内前体的使用的转变。

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