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黄曲霉毒素生物合成的调控:葡萄糖对各种糖酵解酶活性的影响。

Regulation of aflatoxin biosynthesis: effect of glucose on activities of various glycolytic enzymes.

作者信息

Buchanan R L, Lewis D F

出版信息

Appl Environ Microbiol. 1984 Aug;48(2):306-10. doi: 10.1128/aem.48.2.306-310.1984.

DOI:10.1128/aem.48.2.306-310.1984
PMID:6091545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC241508/
Abstract

Catabolism of carbohydrates has been implicated in the regulation of aflatoxin synthesis. To characterize this effect further, the activities of various enzymes associated with glucose catabolism were determined in Aspergillus parasiticus organisms that were initially cultured in peptone-mineral salts medium and then transferred to glucose-mineral salts and peptone-mineral salts media. After an initial increase in activity, the levels of glucose 6-phosphate dehydrogenase, mannitol dehydrogenase, and malate dehydrogenase were lowered in the presence of glucose. Phosphofructokinase activity was greater in the peptone-grown mycelium, but fructose diphosphatase was largely unaffected by carbon source. Likewise, carbon source had relatively little effect on the activities of pyruvate kinase, malic enzyme, isocitrate-NADP dehydrogenase, and isocitrate-NAD dehydrogenase. The results suggest that glucose may, in part, regulate aflatoxin synthesis via a carbon catabolite repression of NADPH-generating and tricarboxylic acid cycle enzymes.

摘要

碳水化合物的分解代谢与黄曲霉毒素合成的调控有关。为了进一步表征这种效应,在最初在蛋白胨 - 矿物盐培养基中培养,然后转移到葡萄糖 - 矿物盐和蛋白胨 - 矿物盐培养基中的寄生曲霉生物体中,测定了与葡萄糖分解代谢相关的各种酶的活性。在活性最初增加之后,在葡萄糖存在下,6 - 磷酸葡萄糖脱氢酶、甘露醇脱氢酶和苹果酸脱氢酶的水平降低。磷酸果糖激酶活性在蛋白胨生长的菌丝体中更高,但果糖二磷酸酶在很大程度上不受碳源的影响。同样,碳源对丙酮酸激酶、苹果酸酶、异柠檬酸 - NADP脱氢酶和异柠檬酸 - NAD脱氢酶的活性影响相对较小。结果表明,葡萄糖可能部分地通过对产生NADPH的酶和三羧酸循环酶的碳分解代谢物阻遏来调节黄曲霉毒素的合成。

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本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
PRODUCTION OF AFLATOXINS IN SUBMERGED CULTURE.深层培养中产黄曲霉毒素的情况。
Appl Microbiol. 1965 Mar;13(2):208-11. doi: 10.1128/am.13.2.208-211.1965.
3
Purification and characterization of mannitol dehydrogenase from Aspergillus parasiticus.寄生曲霉中甘露醇脱氢酶的纯化与特性分析
J Bacteriol. 1982 Jul;151(1):243-50. doi: 10.1128/jb.151.1.243-250.1982.
4
Influence of tricarboxylic acid cycle intermediates and related metabolites on the biosynthesis of aflatoxin by resting cells of Aspergillus flavus.三羧酸循环中间体及相关代谢产物对黄曲霉静止细胞合成黄曲霉毒素的影响。
Appl Environ Microbiol. 1981 Nov;42(5):758-61. doi: 10.1128/aem.42.5.758-761.1981.
5
New perspectives on aflatoxin biosynthesis.黄曲霉毒素生物合成的新视角。
Adv Appl Microbiol. 1983;29:53-92. doi: 10.1016/s0065-2164(08)70354-x.
6
Caffeine inhibition of aflatoxin synthesis: probable site of action.咖啡因对黄曲霉毒素合成的抑制作用:可能的作用位点。
Appl Environ Microbiol. 1984 Jun;47(6):1216-20. doi: 10.1128/aem.47.6.1216-1220.1984.
7
Caffeine inhibition of aflatoxin production: mode of action.咖啡因对黄曲霉毒素产生的抑制作用:作用模式。
Appl Environ Microbiol. 1983 Nov;46(5):1193-200. doi: 10.1128/aem.46.5.1193-1200.1983.
8
The regulation of NADP-linked isocitrate dehydrogenase in Aspergillus nidulans.构巢曲霉中烟酰胺腺嘌呤二核苷酸磷酸(NADP)连接的异柠檬酸脱氢酶的调控
J Gen Microbiol. 1982 Jan;128(1):23-8. doi: 10.1099/00221287-128-1-23.
9
Production of aflatoxins B1 and G1 by Aspergillus flavus in a semisynthetic medium.黄曲霉在半合成培养基中产生黄曲霉毒素B1和G1 。
Appl Microbiol. 1966 May;14(3):378-80. doi: 10.1128/am.14.3.378-380.1966.
10
The relative contribution of acetate and glucose to aflatoxin biosynthesis.乙酸盐和葡萄糖对黄曲霉毒素生物合成的相对贡献。
Biochim Biophys Acta. 1970 Jun;208(3):482-6. doi: 10.1016/0304-4165(70)90222-9.