Collaborative Research: EDGE FGT: Development of a Comprehensive Selection Library to Reconcile Core Metabolic Knowledge Gaps

合作研究:EDGE FGT:开发综合选择库以弥合核心代谢知识差距

基本信息

  • 批准号:
    2319733
  • 负责人:
  • 金额:
    $ 38.27万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Standard Grant
  • 财政年份:
    2023
  • 资助国家:
    美国
  • 起止时间:
    2023-08-15 至 2026-07-31
  • 项目状态:
    未结题

项目摘要

This project is motivated by the large number of genes of unknown function found in sequenced genomes. Genome sequencing and bioinformatics has transformed understanding of the capabilities of living organisms, leading to broad impacts on biotechnology, agriculture, health, and the environment. Despite these advances, the functions of many genes remain unknown, even for well-studied model organisms such as Escherichia coli. In non-model organisms, most functional assignments are not based on direct experimental evidence, but instead are based on sequence homology and/or shared patterns with known genes across datasets. Automated bioinformatics algorithms have increased the rate of genome annotation, but unfortunately fail to assign functions to 40-60% of all new gene sequences, and worse, exhibit a high rate of mis-annotation. These omissions and propagated errors complicate efforts to computationally model, understand, and engineer organisms and higher living systems. For this reason, it is critical to develop tools for rapidly identifying functions of genes in non-model organisms to better understand their genotype-phenotype relationships. This project will generate such tools and resources (algorithms, strains, and plasmids), share them with the broader scientific community, and provide related training to help reduce these gaps in knowledge and accelerate linking genotypes to phenotypes on a large scale. The project will also create systems and synthetic biology research opportunities for undergraduate and graduate students, and involve outreach efforts to engage K-12 students and the general public.This project will address the fundamental problem described above for all biological systems by developing a gene annotation pipeline (GAP) toolbox to identify genotypes and media conditions that select for genes encoding enzymes and transporters that catalyze a metabolic reaction of interest. Synthetic biology methods will then be employed to assemble a library of microbial strains that can select for key metabolic reactions using a small set of non-permissive conditions. Together these tools will be used to close the metabolic knowledge gaps in two important rhizosphere microbes as test cases for the GAP toolbox. The resulting links between genes and reactions will deepen understanding of metabolism in the rhizosphere and enable future basic research on soil as well as novel agricultural biotechnologies. More broadly, improved annotations resulting from this work will be propagated to other sequenced genomes where homologs exist, increasing global understanding of metabolism in other biological systems as well.This project is co-funded by the Genetic Mechanisms program of the Molecular and Cellular Biosciences Division in the Biological Sciences Directorate.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.
该项目的动机是在测序的基因组中发现了大量功能未知的基因。基因组测序和生物信息学改变了对生物体能力的理解,对生物技术、农业、健康和环境产生了广泛的影响。尽管取得了这些进展,许多基因的功能仍然未知,即使是对大肠杆菌等研究充分的模式生物也是如此。在非模式生物中,大多数功能分配不是基于直接的实验证据,而是基于序列同源性和/或跨数据集与已知基因的共享模式。自动化生物信息学算法提高了基因组注释的速度,但不幸的是,未能将功能分配给所有新基因序列的40-60%,更糟糕的是,表现出很高的错误注释率。这些遗漏和传播的错误使计算建模、理解和工程生物体和高等生命系统的努力变得复杂。因此,开发快速鉴定非模式生物中基因功能的工具以更好地了解其基因型-表型关系至关重要。该项目将产生这些工具和资源(算法,菌株和质粒),与更广泛的科学界分享,并提供相关培训,以帮助缩小这些知识差距,并加速大规模地将基因型与表型联系起来。该项目还将为本科生和研究生创造系统和合成生物学研究机会,该项目将通过开发一个基因注释管道(GAP)来解决上述所有生物系统的基本问题。工具箱,以鉴定基因型和培养基条件,其选择编码催化感兴趣的代谢反应的酶和转运蛋白的基因。然后,将采用合成生物学方法来组装微生物菌株库,这些菌株可以使用一小组非许可条件来选择关键的代谢反应。这些工具将一起用于缩小两种重要根际微生物的代谢知识差距,作为GAP工具箱的测试案例。由此产生的基因和反应之间的联系将加深对根际代谢的理解,并使未来对土壤的基础研究以及新的农业生物技术成为可能。更广泛地说,这项工作产生的改进的注释将传播到存在同源物的其他测序基因组,增加全球对其他生物系统代谢的了解。该项目是共同的,该奖项由生物科学理事会分子和细胞生物科学部的遗传机制计划资助。该奖项反映了NSF的法定使命,并通过使用基金会的学术价值和更广泛的影响审查标准。

项目成果

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Costas Maranas其他文献

Biomimetic Membrane Design Principles for Angstrom Scale Separation
  • DOI:
    10.1016/j.bpj.2017.11.2005
  • 发表时间:
    2018-02-02
  • 期刊:
  • 影响因子:
  • 作者:
    Tingwei Ren;Ratul Chowdhury;Peter Butler;Costas Maranas;Manish Kumar
  • 通讯作者:
    Manish Kumar
Data-driven and physics informed modeling of Chinese Hamster Ovary cell bioreactors
  • DOI:
    10.1016/j.compchemeng.2024.108594
  • 发表时间:
    2024-04-01
  • 期刊:
  • 影响因子:
  • 作者:
    Tianqi Cui;Tom Bertalan;Nelson Ndahiro;Pratik Khare;Michael Betenbaugh;Costas Maranas;Ioannis G. Kevrekidis
  • 通讯作者:
    Ioannis G. Kevrekidis

Costas Maranas的其他文献

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{{ truncateString('Costas Maranas', 18)}}的其他基金

Collaborative Research: Designing a Minimized Genome Cyanobacterial Chassis for Efficient Bioproduction
合作研究:设计最小化基因组蓝藻底盘以实现高效生物生产
  • 批准号:
    2037829
  • 财政年份:
    2021
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
Collaborative Research: Systems analysis of the interplay between oxygenic photosynthesis and nitrogen fixation in a unicellular cyanobacterium
合作研究:单细胞蓝藻含氧光合作用与固氮之间相互作用的系统分析
  • 批准号:
    1933793
  • 财政年份:
    2019
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
Collaborative Research: SusChEM: Unlocking the fundamental mechanisms that underlie selectivity in oleochemical producing enzymes
合作研究:SusChEM:解锁油脂化学生产酶选择性的基本机制
  • 批准号:
    1703274
  • 财政年份:
    2017
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
Collaborative Research: From genotype to fluxome to a comprehensive kinetic model of Escherichia coli
合作研究:从基因型到通量组再到大肠杆菌的综合动力学模型
  • 批准号:
    1615646
  • 财政年份:
    2016
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
An Integrated Approach for Computationally Designing and Experimentally Characterizing Fully-Human Antibodies
计算设计和实验表征全人类抗体的综合方法
  • 批准号:
    1133040
  • 财政年份:
    2012
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Continuing Grant
Conference: International Conference on Biochemical and Molecular Engineering, Seattle, WA, June 26-29, 2011
会议:国际生物化学和分子工程会议,华盛顿州西雅图,2011 年 6 月 26-29 日
  • 批准号:
    1102475
  • 财政年份:
    2011
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
Computational Modeling and Design of Cytochrome P450 Reactivity and Substrate Specificity
细胞色素 P450 反应性和底物特异性的计算建模和设计
  • 批准号:
    0967062
  • 财政年份:
    2010
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
Development of Computational Tools and Experimental Verifications for Protein Design
蛋白质设计计算工具的开发和实验验证
  • 批准号:
    0639962
  • 财政年份:
    2007
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
An Integrated Computational Framework for Optimally Allocating Diversity in Directed Evolution Studies
在定向进化研究中优化分配多样性的综合计算框架
  • 批准号:
    0331047
  • 财政年份:
    2003
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant
QSB: Discrete Optimization Techniques for Probing the Performance Limits of Metabolic Networks
QSB:用于探索代谢网络性能极限的离散优化技术
  • 批准号:
    0120277
  • 财政年份:
    2001
  • 资助金额:
    $ 38.27万
  • 项目类别:
    Standard Grant

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