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通过15N核磁共振光谱法测定产甲烷菌中游离氨基酸的周转情况。

Free amino acid turnover in methanogens measured by 15N NMR spectroscopy.

作者信息

Roberts M F, Choi B S, Robertson D E, Lesage S

机构信息

Department of Chemistry, Boston College, Chestnut Hill, Massachusetts 02167.

出版信息

J Biol Chem. 1990 Oct 25;265(30):18207-12.

PMID:2211697
Abstract

Turnover of the nitrogen moiety from free amino acid pools in two thermophilic methanogens, Methanobacterium thermautotrophicum delta H and Methanococcus thermolithotrophicus SN1, has been monitored with 15N NMR spectroscopy. In cells growing exponentially on 15NH4Cl, glutamate was the major soluble 15N-labeled species in both organisms. When the Mb. thermoautotrophicum cells were harvested, washed, and resuspended into medium containing 14NH4Cl, the resonance for [15N]glutamate decreased with a half-life of 0.5 h. This is considerably faster than the turnover rate for the carbon side chain of glutamate (7 h) obtained when a 13CO2 pulse followed by a 12CO2 chase was incorporated into the 15N/14N-labeling experiment. Such behavior is consistent with recycling of the glutamate carbon skeleton via alpha-ketoglutarate after transamination reactions remove the 15N for biosynthesis of other amino acids, nucleic acids, etc. When the cells were in stationary phase, 15N turnover was considerably slower indicating that transaminase activity had also decreased. Mc. thermolithotrophicus has a much more fragile cell wall and easily lyses. To avoid cell loss in the 15N/14N experiment, 15NH+4 growth followed by 14NH4+ dilution was used. In this organism the glutamate-labeled nitrogen turns over quite rapidly (t1/2 approximately 9 min), at a rate comparable to that for the carbon skeleton (t1/2 approximately 10 min). Beta-Glutamate, the second major carbon and nitrogen pool in this organism, turns over its 15N label very slowly. Therefore, this beta-amino acid does not appear to serve as a nitrogen donor in Mc. thermolithotrophicus.

摘要

利用15N核磁共振光谱监测了两种嗜热产甲烷菌——嗜热自养甲烷杆菌δH和嗜热嗜石甲烷球菌SN1中游离氨基酸池中氮部分的周转情况。在以15NH4Cl为氮源指数生长的细胞中,谷氨酸是这两种生物体中主要的可溶性15N标记物质。当收获嗜热自养甲烷杆菌细胞,洗涤后重悬于含有14NH4Cl的培养基中时,[15N]谷氨酸的共振峰以0.5小时的半衰期下降。这比在15N/14N标记实验中,在13CO2脉冲后接着12CO2追踪时谷氨酸碳链的周转速率(7小时)要快得多。这种行为与转氨反应将15N去除用于其他氨基酸、核酸等生物合成后,谷氨酸碳骨架通过α-酮戊二酸的循环利用是一致的。当细胞处于稳定期时,15N周转明显变慢,表明转氨酶活性也降低了。嗜热嗜石甲烷球菌的细胞壁更脆弱,容易裂解。为了避免在15N/14N实验中细胞损失,采用了15NH4+生长后进行14NH4+稀释的方法。在这种生物体中,谷氨酸标记的氮周转相当快(半衰期约为9分钟),速率与碳骨架的周转速率相当(半衰期约为10分钟)。β-谷氨酸是这种生物体中第二大碳和氮库,其15N标记周转非常缓慢。因此,这种β-氨基酸似乎在嗜热嗜石甲烷球菌中不作为氮供体。

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