Identification of a Bis-molybdopterin Intermediate in Molybdenum Cofactor Biosynthesis in Escherichia coli

钼辅因子 大肠杆菌 辅因子 生物合成 化学 生物化学 生物 基因 无机化学
作者
Stefan Reschke,Kajsa G. V. Sigfridsson Clauss,Paul Kaufmann,Nils Leidel,Sebastian Horn,Klaus Gast,Carola Schulzke,Michael Haumann,Silke Leimkühler
出处
期刊:Journal of Biological Chemistry [Elsevier BV]
卷期号:288 (41): 29736-29745 被引量:48
标识
DOI:10.1074/jbc.m113.497453
摘要

The molybdenum cofactor is an important cofactor, and its biosynthesis is essential for many organisms, including humans. Its basic form comprises a single molybdopterin (MPT) unit, which binds a molybdenum ion bearing three oxygen ligands via a dithiolene function, thus forming Mo-MPT. In bacteria, this form is modified to form the bis-MPT guanine dinucleotide cofactor with two MPT units coordinated at one molybdenum atom, which additionally contains GMPs bound to the terminal phosphate group of the MPTs (bis-MGD). The MobA protein catalyzes the nucleotide addition to MPT, but the mechanism of the biosynthesis of the bis-MGD cofactor has remained enigmatic. We have established an in vitro system for studying bis-MGD assembly using purified compounds. Quantification of the MPT/molybdenum and molybdenum/phosphorus ratios, time-dependent assays for MPT and MGD detection, and determination of the numbers and lengths of Mo–S and Mo–O bonds by X-ray absorption spectroscopy enabled identification of a novel bis-Mo-MPT intermediate on MobA prior to nucleotide attachment. The addition of Mg-GTP to MobA loaded with bis-Mo-MPT resulted in formation and release of the final bis-MGD product. This cofactor was fully functional and reconstituted the catalytic activity of apo-TMAO reductase (TorA). We propose a reaction sequence for bis-MGD formation, which involves 1) the formation of bis-Mo-MPT, 2) the addition of two GMP units to form bis-MGD on MobA, and 3) the release and transfer of the mature cofactor to the target protein TorA, in a reaction that is supported by the specific chaperone TorD, resulting in an active molybdoenzyme. Background: Some molybdoenzymes in prokaryotes contain the bis-molybdopterin guanine dinucleotide cofactor. Results: The bis-Mo-MPT cofactor is a novel intermediate in Moco biosynthesis in E. coli. Conclusion: Bis-MGD formed by MobA is fully functional and restores the catalytic activity in apoTorA. Significance: Bis-Mo-MPT assembles spontaneously on MobA prior to forming bis-MGD.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
livefei完成签到,获得积分10
刚刚
M先生发布了新的文献求助10
1秒前
2秒前
科研通AI6.4应助景天采纳,获得10
2秒前
3秒前
3秒前
悦耳静枫完成签到,获得积分10
3秒前
4秒前
4秒前
5秒前
博学为农发布了新的文献求助10
5秒前
5秒前
5秒前
5秒前
6秒前
renbiyun完成签到 ,获得积分10
7秒前
我是老大应助天天采纳,获得10
8秒前
科研黑洞完成签到,获得积分10
8秒前
壮观听芹完成签到,获得积分10
8秒前
cdercder应助thomas采纳,获得10
9秒前
kukupapa完成签到,获得积分10
9秒前
狂野梦菲发布了新的文献求助10
9秒前
YUMI发布了新的文献求助10
9秒前
9秒前
曲ququ发布了新的文献求助10
10秒前
科研通AI6.4应助xwwx采纳,获得10
10秒前
11秒前
bkagyin应助褪色采纳,获得10
12秒前
12秒前
molihuakai应助梦888采纳,获得10
13秒前
小蘑菇应助夏蓉采纳,获得10
15秒前
狂野梦菲完成签到,获得积分20
15秒前
毛77发布了新的文献求助10
15秒前
洪伟华发布了新的文献求助10
16秒前
zzdd发布了新的文献求助10
16秒前
好心情发布了新的文献求助10
16秒前
赘婿应助AA采纳,获得200
17秒前
丘比特应助桃花岛主采纳,获得10
18秒前
18秒前
天天快乐应助大肥子采纳,获得10
18秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7295060
求助须知:如何正确求助?哪些是违规求助? 8913551
关于积分的说明 18873038
捐赠科研通 6961420
什么是DOI,文献DOI怎么找? 3210143
关于科研通互助平台的介绍 2379484
邀请新用户注册赠送积分活动 2186424