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构巢曲霉中硝酸还原酶调控的体内和体外研究。

In vivo and in vitro studies of nitrate reductase regulation in Asperillus nidulans.

作者信息

Dunn-Coleman N S, Pateman J A

出版信息

Mol Gen Genet. 1977 Apr 29;152(3):285-93. doi: 10.1007/BF00693082.

Abstract

Induced wildtype cells of A. nidulans rapidly lost NADPH--linked nitrate reductase activity when subjected to carbon and or nitrogen starvation. A constitutive mutant at the regulatory gene for nitrate reductase, nir Ac 1, rapidly lost nitrate reductase activity upon carbon starvation. This loss of activity is thought to be due to a decrease in the NADPH concentration in the cells. Cell free extracts from wildtype cells grown in the presence of nitrate, rapidly lost their nitrate reductase activity when incubated at 25 degrees C. NADPH prevented this loss of activity. Wildtype cells grown in the presence of nitrate and urea have a higher initial NADPH:NADP+ ratio and cell free extracts from such cells lost their nitrate reductase activity slower than extracts of cells grown with nitrate alone. The Pentose Phosphate Pathway mutant, pppB-1, had a lower NADPH concentration compared with the wildtype grown under the same conditions and cell free extracts lost their nitrate reductase activity more rapidly than the wildtype. Cell free extracts of nirAc-1 and a non-inducible mutant for nitrate reductase, nirA- -14, upon incubation lost little of their nitrate reductase activity.

摘要

构巢曲霉的诱导型野生型细胞在碳饥饿和/或氮饥饿时会迅速丧失与NADPH相关的硝酸还原酶活性。硝酸还原酶调节基因的组成型突变体nir Ac 1在碳饥饿时会迅速丧失硝酸还原酶活性。这种活性丧失被认为是由于细胞中NADPH浓度降低所致。在硝酸盐存在下生长的野生型细胞的无细胞提取物在25℃孵育时会迅速丧失其硝酸还原酶活性。NADPH可防止这种活性丧失。在硝酸盐和尿素存在下生长的野生型细胞具有较高的初始NADPH:NADP + 比率,并且来自此类细胞的无细胞提取物比仅用硝酸盐生长的细胞提取物更慢地丧失其硝酸还原酶活性。戊糖磷酸途径突变体pppB - 1与在相同条件下生长的野生型相比,NADPH浓度较低,并且无细胞提取物比野生型更快地丧失其硝酸还原酶活性。nirAc - 1和硝酸还原酶的非诱导型突变体nirA - - 14的无细胞提取物在孵育时几乎不丧失其硝酸还原酶活性。

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