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热激可保护粗糙脉孢菌的萌发分生孢子免受冻害。

Heat shock protects germinating conidiospores of Neurospora crassa against freezing injury.

作者信息

Guy C L, Plesofsky-Vig N, Brambl R

出版信息

J Bacteriol. 1986 Jul;167(1):124-9. doi: 10.1128/jb.167.1.124-129.1986.

Abstract

Germinating conidiospores of Neurospora crassa that were exposed to 45 degrees C, a temperature that induces a heat shock response, were protected from injury caused by freezing in liquid nitrogen and subsequent thawing at 0 degrees C. Whereas up to 90% of the control spores were killed by this freezing and slow thawing, a prior heat shock increased cell survival four- to fivefold. Survival was determined by three assays: the extent of spore germination in liquid medium, the number of colonies that grew on solid medium, and dry-weight accumulation during exponential growth in liquid culture. The heat shock-induced protection against freezing injury was transient. Spores transferred to normal growth temperature after exposure to heat shock and before freezing lost the heat shock-induced protection within 30 min. Spores subjected to freezing and thawing stress synthesized small amounts of the heat shock proteins that are synthesized in large quantities by cells exposed to 45 degrees C. Pulse-labeling studies demonstrated that neither chilling the spores to 10 degrees C or 0 degrees C in the absence of freezing nor warming the spores from 0 degrees C to 30 degrees C induced heat shock protein synthesis. The presence of the protein synthesis inhibitor cycloheximide during spore exposure to 45 degrees C did not abolish the protection against freezing injury induced by heat shock. Treatment of the cells with cycloheximide before freezing, without exposure to heat shock, itself increased spore survival.

摘要

将粗糙脉孢菌的分生孢子置于45摄氏度(该温度可诱导热休克反应)下使其萌发,这些孢子可免受液氮冷冻及随后在0摄氏度解冻所造成的损伤。在这种冷冻和缓慢解冻过程中,高达90%的对照孢子会死亡,而预先进行热休克可使细胞存活率提高四到五倍。通过三种测定方法来确定存活率:液体培养基中孢子的萌发程度、固体培养基上生长的菌落数量以及液体培养指数增长期间的干重积累。热休克诱导的抗冷冻损伤保护作用是短暂的。在热休克后、冷冻前转移到正常生长温度的孢子在30分钟内失去了热休克诱导的保护作用。遭受冷冻和解冻应激的孢子合成少量热休克蛋白,而暴露于45摄氏度的细胞会大量合成这些蛋白。脉冲标记研究表明,在不存在冷冻的情况下将孢子冷却至10摄氏度或0摄氏度,或者将孢子从0摄氏度加热至30摄氏度,均不会诱导热休克蛋白合成。在孢子暴露于45摄氏度期间存在蛋白质合成抑制剂环己酰亚胺并不会消除热休克诱导的抗冷冻损伤保护作用。在冷冻前用环己酰亚胺处理细胞(未进行热休克)本身会提高孢子存活率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9237/212850/a0514167b5bf/jbacter00206-0136-a.jpg

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