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性菌毛在十二烷基硫酸钠对大肠杆菌性因子和耐药因子的有效消除作用中的特定作用。

Specific role of sex pili in the effective eliminatory action of sodium dodecyl sulfate on sex and drug resistance factors in Escherichia coli.

作者信息

Adachi H, Nakano M, Inuzuka M, Tomoeda M

出版信息

J Bacteriol. 1972 Mar;109(3):1114-24. doi: 10.1128/jb.109.3.1114-1124.1972.

Abstract

Evidence is presented for the specific role of sex pili in the eliminatory action of sodium dodecyl sulfate (SDS) on sex (F) and drug resistance (R) factors in Escherichia coli K-12 strains leading to their loss. SDS at 0.03% concentration lysed JE3100 F(8) (+) (F-gal)/gal(-)fla(-)pil(-) in Penassay broth after they had grown exponentially and reached maximum growth to the extent that the agent at concentrations higher than 1% did. However, the agent was only effective in eliminating sex factors from JE3100 in high frequencies at concentrations higher than 1%. Increase of osmotic pressure of the culture with SDS at concentrations as low as 0.03 to 0.1% by addition of sucrose led to the substantial increase of elimination efficiency. Reconstruction experiments between F(8) (+) and F(-) cells in the SDS culture revealed the selective growth of F(-) cells as well as a delay of maximum growth of F(-) variants derived from F(8) (+) cells, compared with those of F(8) (+) cells, as well as F(-) cells originally added to the culture. The agent was not very effective in eliminating sex factors from JE3427 F(8)m(+)5/fla(-)pil(-) cells which lack the function of production of F pili. F(8)m(+)5 cells showed a sensitivity toward SDS intermediate between those of F(8) (+) and F(-) cells. SDS was further effective in eliminating R factors from KE132 R(100-1) (+)/fla(-)pil(-) cells in high efficiency; however, the action was not efficient with KE133 F(100) (+) cells possibly with fewer sex pili than R(100-1) (+). Action of acridine orange on these F(+) or R(+) strains was found to be different in some aspects from that of SDS.

摘要

有证据表明,性菌毛在十二烷基硫酸钠(SDS)对大肠杆菌K - 12菌株中性(F)因子和耐药(R)因子的消除作用中具有特定作用,这种作用会导致这些因子的丢失。在检测肉汤中,0.03%浓度的SDS在JE3100 F(8) (+)(F - gal)/gal(-)fla(-)pil(-)菌株指数生长并达到最大生长量后,能像浓度高于1%的该试剂一样使其裂解。然而,该试剂只有在浓度高于1%时,才能高效地从JE3100中消除性因子。通过添加蔗糖将SDS浓度低至0.03%至0.1%的培养液渗透压升高,可使消除效率大幅提高。在SDS培养液中F(8) (+)和F(-)细胞之间的重建实验表明,与F(8) (+)细胞以及最初添加到培养液中的F(-)细胞相比,F(-)细胞选择性生长,并且源自F(8) (+)细胞的F(-)变体的最大生长出现延迟。该试剂对缺乏F菌毛产生功能的JE3427 F(8)m(+)5/fla(-)pil(-)细胞消除性因子的效果不太明显。F(8)m(+)5细胞对SDS的敏感性介于F(8) (+)和F(-)细胞之间。SDS能高效地从KE132 R(100 - 1) (+)/fla(-)pil(-)细胞中消除R因子;然而,对KE133 F(100) (+)细胞的作用效率不高,可能是因为其性菌毛比R(100 - 1) (+)细胞少。发现吖啶橙对这些F(+)或R(+)菌株的作用在某些方面与SDS不同。

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