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在黄曲霉毒素途径受阻的寄生曲霉突变体共发酵过程中,通过途径中间体的交叉喂养产生黄曲霉毒素。

Aflatoxin production via cross-feeding of pathway intermediates during cofermentation of aflatoxin pathway-blocked Aspergillus parasiticus mutants.

作者信息

Cleveland T E, Bhatnagar D, Brown R L

机构信息

Southern Regional Research Center, U.S. Department of Agriculture, New Orleans, Louisiana 70124.

出版信息

Appl Environ Microbiol. 1991 Oct;57(10):2907-11. doi: 10.1128/aem.57.10.2907-2911.1991.

DOI:10.1128/aem.57.10.2907-2911.1991
PMID:1746952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC183895/
Abstract

Cofermentation of Aspergillus parasiticus strains (SRRC 163 and SRRC 2043) blocked at different steps in the aflatoxin B1 (AFB1) biosynthetic pathway in a synthetic liquid medium or on seeds (cottonseed, corn kernels, and peanuts) resulted in production of AFB1. Strain SRRC 2043 accumulated O-methylsterigmatocystin (OMST), a late precursor in AFB1 biosynthesis, whereas SRRC 163 accumulated averantin, an early precursor in the pathway. Strain SRRC 2043 secreted large amounts of OMST in culture relative to the amounts of several other pathway intermediates secreted into media (by other AFB1 pathway-blocked strains). AFB1 production occurred even when colonies of SRRC 163 and SRRC 2043 strains (producing no detectable AFB1) were grown together on an agar medium while physically separated from each other by a filter membrane (0.22-micron pore size). In addition, when mycelia of strain SRRC 163 were added to culture filtrates (containing no mycelia but containing secreted OMST) of strain SRRC 2043, AFB1 production occurred. The results suggested a chemical (rather than genetic) mechanism of complementation for AFB1 production between AFB1 pathway-blocked strains, since no mycelial contact was required between these strains for AFB1 production. The mechanism for chemical complementation involves secretion of OMST by SRRC 2043 and subsequent absorption and conversion of OMST to AFB1 by mycelia of strain SRRC 163.

摘要

在合成液体培养基中或在种子(棉籽、玉米粒和花生)上,对黄曲霉毒素B1(AFB1)生物合成途径中不同步骤受阻的寄生曲霉菌株(SRRC 163和SRRC 2043)进行共发酵,结果产生了AFB1。菌株SRRC 2043积累了O-甲基柄曲霉素(OMST),它是AFB1生物合成中的晚期前体,而SRRC 163积累了柄曲菌素,它是该途径中的早期前体。相对于分泌到培养基中的其他几种途径中间体的量(由其他AFB1途径受阻菌株分泌),菌株SRRC 2043在培养物中分泌了大量的OMST。即使SRRC 163和SRRC 2043菌株(不产生可检测到的AFB1)的菌落通过滤膜(孔径0.22微米)彼此物理分离地在琼脂培养基上一起生长时,也会产生AFB1。此外,当将菌株SRRC 163的菌丝体添加到菌株SRRC 2043的培养滤液(不含菌丝体但含有分泌的OMST)中时,会产生AFB1。结果表明,AFB1途径受阻菌株之间产生AFB1的互补机制是化学(而非遗传)机制,因为这些菌株之间产生AFB1不需要菌丝体接触。化学互补机制涉及SRRC 2043分泌OMST,随后菌株SRRC 163的菌丝体将OMST吸收并转化为AFB1。

相似文献

1
Aflatoxin production via cross-feeding of pathway intermediates during cofermentation of aflatoxin pathway-blocked Aspergillus parasiticus mutants.在黄曲霉毒素途径受阻的寄生曲霉突变体共发酵过程中,通过途径中间体的交叉喂养产生黄曲霉毒素。
Appl Environ Microbiol. 1991 Oct;57(10):2907-11. doi: 10.1128/aem.57.10.2907-2911.1991.
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Conversion of a new metabolite to aflatoxin B2 by Aspergillus parasiticus.寄生曲霉将一种新的代谢产物转化为黄曲霉毒素B2 。
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Conversion of dihydro-O-methylsterigmatocystin to aflatoxin B2 by Aspergillus parasiticus.寄生曲霉将二氢-O-甲基柄曲霉素转化为黄曲霉毒素B2 。
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Biochemistry. 1991 Apr 30;30(17):4343-50. doi: 10.1021/bi00231a033.
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Characterization of the critical amino acids of an Aspergillus parasiticus cytochrome P-450 monooxygenase encoded by ordA that is involved in the biosynthesis of aflatoxins B1, G1, B2, and G2.寄生曲霉细胞色素P-450单加氧酶(由ordA编码)的关键氨基酸的特性分析,该酶参与黄曲霉毒素B1、G1、B2和G2的生物合成。
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Association of aflatoxin biosynthesis and sclerotial development in Aspergillus parasiticus.寄生曲霉中黄曲霉毒素生物合成与菌核发育的关联
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Enzymes in aflatoxin B1 biosynthesis: strategies for identifying pertinent genes.黄曲霉毒素B1生物合成中的酶:鉴定相关基因的策略
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Nonfunctionality of Aspergillus sojae aflR in a strain of Aspergillus parasiticus with a disrupted aflR gene.在一株寄生曲霉中,米曲霉aflR基因缺失导致其功能丧失,该寄生曲霉的aflR基因已被破坏。
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本文引用的文献

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INCORPORATION OF LABELLED COMPOUNDS INTO AFLATOXINS.标记化合物掺入黄曲霉毒素中。
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New perspectives on aflatoxin biosynthesis.黄曲霉毒素生物合成的新视角。
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Conversion of a new metabolite to aflatoxin B2 by Aspergillus parasiticus.寄生曲霉将一种新的代谢产物转化为黄曲霉毒素B2 。
Appl Environ Microbiol. 1987 Dec;53(12):2804-7. doi: 10.1128/aem.53.12.2804-2807.1987.
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Purification and characterization of a methyltransferase from Aspergillus parasiticus SRRC 163 involved in aflatoxin biosynthetic pathway.寄生曲霉SRRC 163中参与黄曲霉毒素生物合成途径的一种甲基转移酶的纯化与特性分析
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Individual reaction requirements of two enzyme activities, isolated from Aspergillus parasiticus, which together catalyze conversion of sterigmatocystin to aflatoxin B1.从寄生曲霉中分离出的两种酶活性的个体反应需求,它们共同催化柄曲霉素转化为黄曲霉毒素B1。
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Appearance of enzyme activities catalyzing conversion of sterigmatocystin to aflatoxin B1 in late-growth-phase Aspergillus parasiticus cultures.在寄生曲霉培养物生长后期,催化柄曲霉素转化为黄曲霉毒素B1的酶活性的出现。
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9
Identification of O-methylsterigmatocystin as an aflatoxin B1 and G1 precursor in Aspergillus parasiticus.鉴定寄生曲霉中O-甲基柄曲霉素作为黄曲霉毒素B1和G1的前体。
Appl Environ Microbiol. 1987 May;53(5):1028-33. doi: 10.1128/aem.53.5.1028-1033.1987.
10
Averufanin is an aflatoxin B1 precursor between averantin and averufin in the biosynthetic pathway.阿弗菌素是生物合成途径中阿弗拉菌素和阿弗菌素之间的黄曲霉毒素B1前体。
Appl Environ Microbiol. 1987 Jan;53(1):14-6. doi: 10.1128/aem.53.1.14-16.1987.