RUI: Methanogenesis from quaternary amines

RUI:季胺产甲烷

基本信息

  • 批准号:
    1818178
  • 负责人:
  • 金额:
    $ 34.3万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Standard Grant
  • 财政年份:
    2018
  • 资助国家:
    美国
  • 起止时间:
    2018-08-01 至 2023-07-31
  • 项目状态:
    已结题

项目摘要

This project will investigate mechanisms by which methane-producing microorganisms can utilize an important and understudied class of compounds to produce methane. Methane, the key component of natural gas, plays an important role in global carbon cycling and atmospheric processes. Some methane-producing microbes (methanogens) have recently been shown to convert a group of compounds called quaternary amines (QAs) to methane. QAs are abundant compounds in many different environments, and methanogenesis in the human gut has been linked to the development of heart disease. Current knowledge of how methanogens can convert QAs to methane and how prevalent this process is in the environment is distinctly lacking. This gap in knowledge leads to potential inaccuracies in computer-generated models predicting the role of methanogenesis on Earth's atmosphere. This research project will address this gap in knowledge by 1) investigating the physiological mechanisms of methanogenesis via QAs and 2) identifying and quantifying the microorganisms responsible for this process in different environments. This research will also benefit students at the Miami University Hamilton, part of a community-based division of Miami University that serves students from first-generation, lower socioeconomic status, and under-represented minority groups. These students will contribute to the research project through classroom activities and undergraduate research.Quaternary amines (QAs) are abundant natural compounds that have recently emerged as important substrates for microbes in anoxic environments, including methanogens. The breakdown of QAs has direct implications for diverse processes from global biogeochemical cycling to atherosclerosis in humans. Understanding of the mechanisms of anaerobic catabolism of QAs by methanogenic archaea, namely QA demethylation, is lacking. Early data suggest that pyrrolysine-lacking (non-pyl) methyltransferases from the COG5598 protein family are involved in QA-dependent methanogenesis along with cognate corrinoid binding proteins, but these pathways have not been elucidated. Determining the function of multiple enzymes from this family will facilitate better identification of the role of members of COG5598 in methane production. The central hypothesis of this proposal is that non-pyl COG5598 enzymes are responsible for QA demethylation and initiation of QA-dependent methanogenesis as part of a three-component corrinoid-dependent methyl transfer pathway, and that organisms encoding these pathways can be identified within the environment. In this work the investigators will: 1) identify pathways for QA-dependent methanogenesis from glycine betaine and tetramethylammonium using comparative proteomics and biochemistry techniques, and 2) determine the identities and relative abundance of predicted QA-utilizing methanogens in different environments.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
该项目将研究产甲烷微生物利用一类重要且未被充分研究的化合物来生产甲烷的机制。甲烷是天然气的关键成分,在全球碳循环和大气过程中发挥着重要作用。一些产甲烷微生物(产甲烷菌)最近被证明可以将一组名为季胺(QA)的化合物转化为甲烷。QA在许多不同的环境中都是丰富的化合物,人类肠道中的甲烷生成与心脏病的发展有关。目前对产甲烷菌如何将QAS转化为甲烷,以及这一过程在环境中的普遍程度的了解显然是缺乏的。这种知识上的差距导致计算机生成的模型在预测甲烷生成在地球大气中的作用时存在潜在的不准确。这项研究项目将通过1)通过QAS调查产甲烷的生理机制和2)识别和量化在不同环境中负责这一过程的微生物来解决这一知识差距。这项研究也将使迈阿密大学汉密尔顿分校的学生受益,该分校是迈阿密大学以社区为基础的部门的一部分,为来自第一代、社会经济地位较低和代表性不足的少数群体的学生提供服务。这些学生将通过课堂活动和本科生研究为研究项目做出贡献。季胺(QAS)是一种丰富的天然化合物,最近成为缺氧环境中微生物的重要底物,包括产甲烷菌。QAS的崩溃对从全球生物地球化学循环到人类动脉粥样硬化的各种过程都有直接的影响。产甲烷古菌对QA的厌氧分解代谢机制,即QA去甲基化,目前还缺乏了解。早期的数据表明,COG5598蛋白家族中缺乏吡咯赖氨酸(非pyl)的甲基转移酶与同源皮质激素结合蛋白一起参与了依赖QA的甲烷化作用,但这些途径尚未阐明。确定该家族中多个酶的功能将有助于更好地识别COG5598成员在甲烷产生中的作用。这一提议的中心假设是,作为依赖皮质醇的三组分甲基转移途径的一部分,非pyl COG5598酶负责QA去甲基化和启动QA依赖的甲烷化,并且编码这些途径的生物可以在环境中被识别。在这项工作中,研究人员将:1)使用比较蛋白质组学和生物化学技术确定甘氨酸甜菜碱和四甲基铵生成依赖QA的甲烷的途径,2)确定预测的利用QA的甲烷菌在不同环境中的身份和相对丰度。该奖项反映了NSF的法定使命,并通过使用基金会的智力优势和更广泛的影响审查标准进行评估,被认为值得支持。

项目成果

期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Examination of the Glycine Betaine-Dependent Methylotrophic Methanogenesis Pathway: Insights Into Anaerobic Quaternary Amine Methylotrophy
  • DOI:
    10.3389/fmicb.2019.02572
  • 发表时间:
    2019-11-07
  • 期刊:
  • 影响因子:
    5.2
  • 作者:
    Creighbaum, Adam J.;Ticak, Tomislav;Ferguson, Donald J., Jr.
  • 通讯作者:
    Ferguson, Donald J., Jr.
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Donald Ferguson其他文献

Ethnic dental analysis of shovel and Carabelli's traits in a Chinese population.
中国人群铲子和卡拉贝利特征的民族牙科分析。
  • DOI:
    10.1111/j.1834-7819.1999.tb00534.x
  • 发表时间:
    1999
  • 期刊:
  • 影响因子:
    2.1
  • 作者:
    John W. Hsu;P. Tsai;T. Hsiao;Hong;Li M. Lin;Keh‐Min Liu;Hsin S. Yu;Donald Ferguson
  • 通讯作者:
    Donald Ferguson
143 Race and clinical outcome in breast cancer: A 40-year follow-up
  • DOI:
    10.1016/0360-3016(95)97806-c
  • 发表时间:
    1995-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Ruth Heimann;Donald Ferguson;Claire Powers;Wendy Recant;Ralph R. Weichselbaum;Samuel Hellman
  • 通讯作者:
    Samuel Hellman
Assessing the impact of the COVID-19 pandemic on the quality of evidence reported in the leading orthodontic journals
评估 COVID-19 大流行对领先正畸期刊中报告的证据质量的影响
  • DOI:
    10.25259/apos_43_2024
  • 发表时间:
    2024
  • 期刊:
  • 影响因子:
    0.4
  • 作者:
    Khadijah Magaji Abubakar;Nada E. Tashkandi;Donald Ferguson;Maha Fouad;Eman Allam
  • 通讯作者:
    Eman Allam
Foreword special issue on cloud computing and services science
  • DOI:
    10.1007/s00607-016-0519-4
  • 发表时间:
    2016-10-13
  • 期刊:
  • 影响因子:
    2.800
  • 作者:
    Markus Helfert;Donald Ferguson;Víctor Méndez Muñoz
  • 通讯作者:
    Víctor Méndez Muñoz
Potassium carbonate decomposition modeling within rotating detonation engines for direct power extraction applications
  • DOI:
    10.1016/j.combustflame.2022.112263
  • 发表时间:
    2022-10-01
  • 期刊:
  • 影响因子:
  • 作者:
    Clinton R. Bedick;Charlotte Albunio;Peter Strakey;Donald Ferguson;Rigel Woodside
  • 通讯作者:
    Rigel Woodside

Donald Ferguson的其他文献

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