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地衣芽孢杆菌生长细胞和原生质体分泌青霉素酶的特性。

Characteristics of penicillinase secretion by growing cells and protoplasts of Bacillus licheniformis.

作者信息

Sargent M G, Ghosh B K, Lampen J O

出版信息

J Bacteriol. 1969 Feb;97(2):820-6. doi: 10.1128/jb.97.2.820-826.1969.

Abstract

Cultures of the inducible penicillinase-producing strain 749 of Bacillus licheniformis, induced with small amounts of benzylpenicillin, synthesized penicillinase at a high rate for a short period, after which the rate of synthesis slowly declined. During the period of active synthesis, the rate of secretion, as a fraction of the level of cell-bound penicillinase (which is originally high), gradually decreased to a constant level. Chloramphenicol, at a concentration (40 mug/ml) which completely inhibited synthesis of penicillinase, partially inhibited secretion if added during the period of active synthesis. During the phase of reduced synthesis, chloramphenicol was without effect on secretion. Penicillinase secretion, by actively growing cultures of the constitutive penicillinase-producing mutant 749/C, was inhibited by 75% immediately after addition of chloramphenicol. The secretion of part of the penicillinase released during active growth is probably dependent on synthesis of penicillinase, but part of the secreted penicillinase can be released in the absence of synthesis. Protoplasts were obtained from which periplasmic penicillinase has been removed, and these protoplasts were capable of substantial growth and penicillinase synthesis without lysis. At pH 7.5, there was no net incorporation of penicillinase into the cell membrane; the enzyme released was almost entirely of the exo form and was roughly equivalent to the amount of new enzyme formed. At pH 6.0, there was some incorporation of penicillinase into the plasma membrane, and approximately half of the extracellular penicillinase was in the exo form; the remainder perhaps represented membrane fragments. In the presence of chloramphenicol, a small amount of penicillinase was released at pH 7.5 as the exo form; at pH 6.0, practically none was released. We suggest that, with the removal from protoplasts of the periplasmic penicillinase-containing particles, a restriction on secretion has been lifted.

摘要

用少量苄青霉素诱导地衣芽孢杆菌的诱导型产青霉素酶菌株749,该菌株在短时间内高速合成青霉素酶,之后合成速率缓慢下降。在活跃合成期,分泌速率作为细胞结合青霉素酶水平(最初较高)的一部分,逐渐降至恒定水平。氯霉素浓度为40微克/毫升时可完全抑制青霉素酶的合成,若在活跃合成期添加则会部分抑制分泌。在合成减少阶段,氯霉素对分泌无影响。组成型产青霉素酶突变体749/C的活跃生长培养物分泌青霉素酶,添加氯霉素后立即受到75%的抑制。活跃生长期间释放的部分青霉素酶的分泌可能依赖于青霉素酶的合成,但部分分泌的青霉素酶可在无合成的情况下释放。获得了已去除周质青霉素酶的原生质体,这些原生质体能够大量生长并合成青霉素酶而不裂解。在pH 7.5时,青霉素酶没有净掺入细胞膜;释放的酶几乎完全是外切型,且大致相当于新形成的酶量。在pH 6.0时,有一些青霉素酶掺入质膜,细胞外青霉素酶约一半是外切型;其余部分可能代表膜片段。在氯霉素存在的情况下,在pH 7.5时有少量青霉素酶以外切型释放;在pH 6.0时,几乎没有释放。我们认为,随着含周质青霉素酶颗粒从原生质体中去除,对分泌的限制被解除。

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J Gen Microbiol. 1967 Aug;48(2):261-8. doi: 10.1099/00221287-48-2-261.
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The formation of penicillinase by cysteine-starved auxotrophs of Bacillus licheniformis.
Biochim Biophys Acta. 1965 Oct 11;108(2):297-305. doi: 10.1016/0005-2787(65)90014-6.
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Rapid fixed-time assay for penicillinase.青霉素酶快速定时测定法
J Bacteriol. 1968 Apr;95(4):1493-4. doi: 10.1128/jb.95.4.1493-1494.1968.

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