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通过乙二胺四乙酸-三(羟甲基)氨基甲烷从存活的副流感嗜血杆菌中释放膜成分。

Release of membrane components from viable Haemophilus parainfluenzae by ethylenediaminetetraacetic acid-tris(hydroxymethyl)-aminomethane.

作者信息

Tucker A N, White D C

出版信息

J Bacteriol. 1970 May;102(2):498-507. doi: 10.1128/jb.102.2.498-507.1970.

Abstract

Logarithmically growing Haemophilus parainfluenzae lost 15 to 20% of the phospholipids, demethyl vitamin K(2), 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 K(2), 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.

摘要

对数生长期的副流感嗜血杆菌在乙二胺四乙酸(EDTA)-三(羟甲基)氨基甲烷(Tris)中孵育10分钟后,会损失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,以及50%的脂多糖。膜成分的这种损失并未导致活力丧失,损失的成分以膜碎片的形式在周围缓冲液中回收。膜碎片中回收的磷脂比残余物中的磷脂比活性略低。部分细胞的裂解并不能解释膜成分的释放,因为细胞既没有丧失6-磷酸葡萄糖脱氢酶活性,也没有丧失脱氧核糖核酸。处理后的细胞在渗透压方面是稳定的,且所含的各磷脂比例与预处理前的细胞相同。延长EDTA-Tris处理时间不会导致磷脂或去甲基维生素K(2)进一步损失,但会导致活力下降。如果细胞在10分钟后回到生长培养基中,它们会立即以预处理前的速率恢复生长。在恢复期生长过程中,磷脂以预处理前的比例呈对数增加,尽管周转率显著下降,且从使用细胞外脂质前体转变为使用细胞内前体库。

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