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与黄曲霉毒素生物合成相关的nor-1和ver-1基因的调控表达。

Regulated expression of the nor-1 and ver-1 genes associated with aflatoxin biosynthesis.

作者信息

Skory C D, Chang P K, Linz J E

机构信息

Department of Food Science and Human Nutrition, Michigan State University, East Lansing 48824.

出版信息

Appl Environ Microbiol. 1993 May;59(5):1642-6. doi: 10.1128/aem.59.5.1642-1646.1993.

Abstract

RNA transcript accumulation for the ver-1 and nor-1 genes, which are associated with aflatoxin biosynthesis in the fungus Aspergillus parasiticus, was measured before and during aflatoxin production in liquid shake culture. Transcripts were not detected until near the end of trophophase (growth phase) and could still be observed well into stationary phase during batch fermentation in an aflatoxin-supporting growth medium. Maximum accumulation of both transcripts occurred just prior to the onset of stationary phase. Aflatoxin B1 was first detected approximately 8 h after the appearance of the ver-1 and nor-1 transcripts. In contrast, maximum transcript accumulation for the pyrG gene (encoding orotidine monophosphate decarboxylase), which is involved in primary metabolism, was observed at the onset of trophophase when the ver-1 and nor-1 transcripts could not be detected. Accumulation of the ver-1 and nor-1 transcripts was also studied following a nutritional shift from a non-aflatoxin-supporting medium (peptone mineral salts [PMS]) to a glucose-containing medium (glucose mineral salts [GMS]), which does support aflatoxin biosynthesis. Transcripts from ver-1 and nor-1 could not be detected on PMS medium but did accumulate approximately 4 to 7 h following transfer to GMS medium. Additionally, aflatoxins were not detected in PMS medium but were observed to accumulate within 24 h after the shift from PMS to GMS. These data suggest that aflatoxin biosynthesis is in part regulated by the accumulation of the ver-1 and nor-1 transcripts.

摘要

在寄生曲霉液体摇瓶培养中黄曲霉毒素产生之前及期间,对与黄曲霉毒素生物合成相关的ver-1和nor-1基因的RNA转录物积累情况进行了测定。直到营养生长期(生长阶段)接近尾声时才检测到转录物,并且在黄曲霉毒素支持生长培养基中的分批发酵过程中,直到稳定期仍能很好地观察到转录物。两种转录物的最大积累量都发生在稳定期开始之前。黄曲霉毒素B1在ver-1和nor-1转录物出现后约8小时首次被检测到。相比之下,参与初级代谢的pyrG基因(编码乳清苷单磷酸脱羧酶)的转录物最大积累量在营养生长期开始时被观察到,此时ver-1和nor-1转录物无法被检测到。在从非黄曲霉毒素支持培养基(蛋白胨矿物盐[PMS])转变为含葡萄糖培养基(葡萄糖矿物盐[GMS])后,也对ver-1和nor-1转录物的积累情况进行了研究,后者确实支持黄曲霉毒素生物合成。在PMS培养基上未检测到ver-1和nor-1的转录物,但在转移到GMS培养基后约4至7小时确实积累了转录物。此外,在PMS培养基中未检测到黄曲霉毒素,但在从PMS转变为GMS后24小时内观察到其积累。这些数据表明,黄曲霉毒素生物合成部分受ver-1和nor-1转录物积累的调控。

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