Sieg Alex G, Trotter Pamela J
Guehler Biochemistry Laboratory, Department of Chemistry, Augustana College, 639-38th Street, Rock Island, IL 61201, United States.
Guehler Biochemistry Laboratory, Department of Chemistry, Augustana College, 639-38th Street, Rock Island, IL 61201, United States.
Microbiol Res. 2014 Sep-Oct;169(9-10):709-16. doi: 10.1016/j.micres.2014.02.004. Epub 2014 Feb 17.
In Saccharomyces cerevisiae, the glutamate dehydrogenase (GDH) enzymes play a pivotal role in glutamate biosynthesis and nitrogen assimilation. It has been proposed that, in GDH-deficient yeast, either the proline utilization (PUT) or the glutamine synthetase-glutamate synthase (GS/GOGAT) pathway serves as the alternative pathway for glutamate production and nitrogen assimilation to the exclusion of the other. Using a gdh-null mutant (gdh1Δ2Δ3Δ), this ambiguity was addressed using a combination of growth studies and pathway-specific enzyme assays on a variety of nitrogen sources (ammonia, glutamine, proline and urea). The GDH-null mutant was viable on all nitrogen sources tested, confirming that alternate pathways for nitrogen assimilation exist in the gdh-null strain. Enzyme assays point to GS/GOGAT as the primary alternative pathway on the preferred nitrogen sources ammonia and glutamine, whereas growth on proline required both the PUT and GS/GOGAT pathways. In contrast, growth on glucose-urea media elicited a decrease in GOGAT activity along with an increase in activity of the PUT pathway specific enzyme Δ(1)-pyrroline-5-carboxylate dehydrogenase (P5CDH). Together, these results suggest the alternative pathway for nitrogen assimilation in strains lacking the preferred GDH-dependent route is nitrogen source dependent and that neither GS/GOGAT nor PUT serves as the sole compensatory pathway.
在酿酒酵母中,谷氨酸脱氢酶(GDH)在谷氨酸生物合成和氮同化过程中起着关键作用。有人提出,在缺乏GDH的酵母中,脯氨酸利用(PUT)途径或谷氨酰胺合成酶-谷氨酸合酶(GS/GOGAT)途径作为谷氨酸产生和氮同化的替代途径,二者相互排斥。利用gdh基因缺失突变体(gdh1Δ2Δ3Δ),通过对多种氮源(氨、谷氨酰胺、脯氨酸和尿素)进行生长研究和特定途径的酶活性测定相结合的方法,解决了这一模糊问题。GDH基因缺失突变体在所有测试的氮源上均能存活,证实了gdh基因缺失菌株中存在氮同化的替代途径。酶活性测定表明,在首选氮源氨和谷氨酰胺上,GS/GOGAT是主要的替代途径,而在脯氨酸上生长则需要PUT和GS/GOGAT途径。相反,在葡萄糖-尿素培养基上生长会导致GOGAT活性降低,同时PUT途径特异性酶Δ(1)-吡咯啉-5-羧酸脱氢酶(P5CDH)的活性增加。总之,这些结果表明,在缺乏首选的依赖GDH途径的菌株中,氮同化的替代途径是依赖氮源的,并且GS/GOGAT和PUT都不是唯一的补偿途径。