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溶菌酶在体外对粗球孢子菌球形体期生长的抑制作用。

Inhibition by lysozyme of growth of the spherule phase of Coccidioides immitis in vitro.

作者信息

Collins M S, Pappagianis D

出版信息

Infect Immun. 1974 Sep;10(3):616-23. doi: 10.1128/iai.10.3.616-623.1974.

DOI:10.1128/iai.10.3.616-623.1974
PMID:4426701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC422996/
Abstract

Development of mature endosporulating spherules from an endospore inoculum was markedly inhibited by human or hen egg-white (HEW) lysozyme at 5 mug/ml. Mature spherules formed in medium containing 5 mug per lysozyme per ml (3.3 x 10(-7) M) were approximately 50% smaller than control spherules. In addition, lysozyme induced a large portion of the endospore inoculum to revert to the mycelial growth phase. Increasing lysozyme concentrations to 10 or 20 mug/ml prompted a nearly complete reversion of the inoculum to the mycelial phase. Mature endosporulating spherules removed from growth medium and resuspended in a solution of human or HEW lysozyme at 18 mug/ml in distilled water prompted leakage of four to five times as much of materials absorbing maximally at 260 nm into the supernatant as untreated control spherules during 90 min of incubation. This four- to fivefold increase in nucleotide loss was evident at 4, 25, and 37 C. The permeability of 1-day-old immature spherules and 8-day-old endospores was considerably altered by lysozyme treatment of cells suspended in distilled water. Large amounts of potassium and nucleotides were rapidly lost by each type of cell when treated with 20 mug of lysozyme per ml. After 270 min of exposure to lysozyme, 98% of the immature spherules and 25% of the endospores were nonviable. Lysozyme adsorption by formalin-killed spherules in the presence of varying concentrations of calcium ion and the rapid alteration of permeability seen after lysozyme treatment suggested that the cell membrane was damaged as a result of binding lysozyme.

摘要

人或鸡蛋清(HEW)溶菌酶在5微克/毫升时,能显著抑制由内生孢子接种体发育成成熟的产内生孢子小球。在每毫升含5微克溶菌酶(3.3×10⁻⁷M)的培养基中形成的成熟小球比对照小球小约50%。此外,溶菌酶还能诱导大部分内生孢子接种体回复到菌丝生长阶段。将溶菌酶浓度提高到10或20微克/毫升,会促使接种体几乎完全回复到菌丝阶段。从生长培养基中取出成熟的产内生孢子小球,重悬于蒸馏水中含18微克/毫升人或HEW溶菌酶的溶液中,在90分钟的孵育过程中,与未处理的对照小球相比,会有四到五倍之多的在260纳米处有最大吸收的物质泄漏到上清液中。在4℃、25℃和37℃时,核苷酸损失增加四到五倍是明显的。用溶菌酶处理悬浮在蒸馏水中的细胞后,1日龄未成熟小球和8日龄内生孢子的通透性发生了显著改变。当用每毫升20微克溶菌酶处理时,每种类型的细胞都会迅速损失大量的钾和核苷酸。在接触溶菌酶270分钟后,98%的未成熟小球和25%的内生孢子失去活力。在不同浓度钙离子存在下,福尔马林灭活小球对溶菌酶的吸附以及溶菌酶处理后迅速出现的通透性改变表明,细胞膜因结合溶菌酶而受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/c191f9b9d1db/iai00249-0211-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/d87e3fa95123/iai00249-0209-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/d84590df55bd/iai00249-0209-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/7be7099c4f75/iai00249-0210-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/f0cae1e16dc3/iai00249-0211-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/c191f9b9d1db/iai00249-0211-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/d87e3fa95123/iai00249-0209-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/d84590df55bd/iai00249-0209-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/7be7099c4f75/iai00249-0210-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/f0cae1e16dc3/iai00249-0211-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0db/422996/c191f9b9d1db/iai00249-0211-b.jpg

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本文引用的文献

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