Biosynthetic Pathways of Glycerol Accumulation under Salt Stress in Aspergillus nidulans

Rajendra J. Redkar, Robert D. Locy, Narendra K. Singh
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引用次数: 39

Abstract

Redkar, R. J., Locy. R. D., and Singh, N. K. 1995. Biosynthetic pathways of glycerol accumulation under salt stress in Aspergillus nidulans. Experimental Mycology 19, 241-246. A culture of Aspergillus nidulans (FGSC 359) was gradually adapted for growth in media containing up to 2 M NaCl or was exposed to a salt shock with 2 M NaCl. The intracellular glycerol level increased by about 7.9-fold in salt-adapted and 2.4-fold in salt-shocked cultures when compared to the unadapted culture. The biosynthetic pathway involved in the accumulation of glycerol was investigated under long-term salt adaptation and short-term salt shock. Glycerol 3-phosphate dehydrogenase (EC 1.1.1.8) was induced 1.4-fold in salt-shocked but not in salt-adapted cultures. An alternate enzymatic pathway involving glycerol dehydrogenase (NADP+-dependent) utilizing dihydroxyacetone (DHA) and/or DL-glyceraldehyde (DL-GAD) was induced by NaCl. DHA-dependent glycerol dehydrogenase activity was induced about 6.3-fold in salt adapted and 1.35-fold in salt-shocked cultures, while DL-GAD-dependent activity was induced about 6.1-fold in salt-adapted and 1.2-fold in salt shocked cultures. However, the level of glycerol dehydrogenase activity with DL-GAD as substrate was 7% of the DHA-dependent activity. We conclude that a salt-inducible NADP+-dependent glycerol dehydrogenase activity electrophoretically indistinguishable from previously described glycerol dehydrogenase I results in glycerol accumulation in salt-stressed A. nidulans.

盐胁迫下中性曲霉甘油积累的生物合成途径
瑞德卡,r.j.,洛伊。r.d.和Singh, n.k. 1995。中性曲霉在盐胁迫下甘油积累的生物合成途径。真菌学学报,19,241-246。细粒曲霉(Aspergillus nidulans, FGSC 359)培养物逐渐适应在含高达2 M NaCl的培养基中生长或暴露于2 M NaCl的盐冲击中。与未适应的培养相比,盐适应培养的细胞内甘油水平增加了约7.9倍,盐冲击培养的细胞内甘油水平增加了2.4倍。研究了长期盐适应和短期盐休克下参与甘油积累的生物合成途径。甘油3-磷酸脱氢酶(EC 1.1.1.8)在盐休克培养中被诱导1.4倍,而在盐适应培养中没有。NaCl诱导了甘油脱氢酶(NADP+依赖)利用二羟基丙酮(DHA)和/或dl -甘油醛(DL-GAD)的替代酶途径。dha依赖的甘油脱氢酶活性在盐适应培养中诱导为6.3倍,在盐冲击培养中诱导为1.35倍,而dl - gad依赖的甘油脱氢酶活性在盐适应培养中诱导为6.1倍,在盐冲击培养中诱导为1.2倍。然而,以DL-GAD为底物的甘油脱氢酶活性水平是dha依赖活性的7%。我们得出结论,盐诱导的NADP+依赖的甘油脱氢酶活性在电泳上与先前描述的甘油脱氢酶I难以区分,导致盐胁迫下a . nidulans的甘油积累。
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