Computational modeling and evolutionary implications of biochemical reactions in bacterial microcompartments

被引:4
|
作者
Huffine, Clair A. [1 ,2 ,3 ,4 ]
Wheeler, Lucas C. [5 ]
Wing, Boswell [6 ]
Cameron, Jeffrey C. [2 ,3 ,7 ]
机构
[1] Univ Colorado Boulder, BioFrontiers Inst, 3415 Colorado Ave, Boulder, CO 80309 USA
[2] Univ Colorado, Dept Biochem, Boulder, CO 80309 USA
[3] Univ Colorado, Renewable & Sustainable Energy Inst, Boulder, CO 80309 USA
[4] Univ Colorado, BioFrontiers Inst, Interdisciplinary Quantitat Biol Program IQ Biol, Boulder, CO 80309 USA
[5] Univ Colorado, Dept Ecol & Evolutionary Biol, Boulder, CO 80309 USA
[6] Dept Geol Sci, Boulder, CO 80309 USA
[7] Natl Renewable Energy Lab, Golden, CO 80401 USA
基金
美国国家科学基金会;
关键词
INORGANIC CARBON FLUXES; SYNECHOCOCCUS PCC7942; CARBOXYSOME SHELL; ANHYDRASE; PHOTOSYNTHESIS; CO2; DIOXIDE; RUBISCO; BICARBONATE; DIVERSITY;
D O I
10.1016/j.mib.2021.10.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacterial microcompartments (BMCs) are proteinencapsulated compartments found across at least 23 bacterial phyla. BMCs contain a variety of metabolic processes that share the commonality of toxic or volatile intermediates, oxygen-sensitive enzymes and cofactors, or increased substrate concentration for magnified reaction rates. These compartmentalized reactions have been computationally modeled to explore the encapsulated dynamics, ask evolutionary-based questions, and develop a more systematic understanding required for the engineering of novel BMCs. Many crucial aspects of these systems remain unknown or unmeasured, such as substrate permeabilities across the protein shell, feasibility of pH gradients, and transport rates of associated substrates into the cell. This review explores existing BMC models, dominated in the literature by cyanobacterial carboxysomes, and highlights potentially important areas for exploration.
引用
收藏
页码:15 / 23
页数:9
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