Abstract
The strong advances in synthetic biology enable the engineering of novel functions and complex biological features in unprecedented ways, such as implementing synthetic autotrophic metabolism into heterotrophic hosts. A key challenge for the sustainable production of fuels and chemicals entails the engineering of synthetic autotrophic organisms that can effectively and efficiently fix carbon dioxide by using sustainable energy sources. This challenge involves the integration of carbon fixation and energy uptake systems. A variety of carbon fixation pathways and several types of photosystems and other energy uptake systems can be chosen and, potentially, modularly combined to design synthetic autotrophic metabolism. Prior to implementation, these designs can be evaluated by the combination of several computational pathway analysis techniques. Here we present a systematic, integrated in silico analysis of photo-electro-autotrophic pathway designs, consisting of natural and synthetic carbon fixation pathways, a proton-pumping rhodopsin photosystem for ATP regeneration and an electron uptake pathway. We integrated Flux Balance Analysis of the heterotrophic chassis Escherichia coli with kinetic pathway analysis and thermodynamic pathway analysis (Max-min Driving Force). The photo-electro-autotrophic designs are predicted to have a limited potential for anaerobic, autotrophic growth of E. coli, given the relatively low ATP regenerating capacity of the proton pumping rhodopsin photosystems and the high ATP maintenance of E. coli. If these factors can be tackled, our analysis indicates the highest growth potential for the natural reductive tricarboxylic acid cycle and the synthetic pyruvate synthase–pyruvate carboxylate -glyoxylate bicycle. Both carbon fixation cycles are very ATP efficient, while maintaining fast kinetics, which also results in relatively low estimated protein costs for these pathways. Furthermore, the synthetic bicycles are highly thermodynamic favorable under conditions analysed. However, the most important challenge identified for improving photo-electro-autotrophic growth is increasing the proton-pumping rate of the rhodopsin photosystems, allowing for higher ATP regeneration. Alternatively, other designs of autotrophy may be considered, therefore the herein presented integrated modeling approach allows synthetic biologists to evaluate and compare complex pathway designs before experimental implementation.
Highlights
One of the current grand societal and technological challenges is to establish sustainable production processes for chemicals and fuels
Major advances in synthetic biology start to allow engineering of complex features related to autotrophy into heterotrophic chassis microorganisms, such as Escherichia coli
We propose the Pathway Protein Burden (PPB) (g protein/gCDW) as a method to estimate the fraction of cellular dry weight that needs to be dedicated to carbon fixation enzymes to produce pyruvate from CO2 for the growth rate predicted by Flux Balance Analysis (FBA)
Summary
One of the current grand societal and technological challenges is to establish sustainable production processes for chemicals and fuels. Autotrophic, synthetic microorganisms require integration of subsystems for both carbon fixation and energy uptake to regenerate electron donors and ATP Those subsystems need to be integrated into properly evaluated designs before going into the challenging, time-consuming and expensive process of experimental implementation. We present an in silico analysis of different designs for so called anaerobic photo-electro-autotrophy in E. coli These designs consist of both uptake pathways for electron donors and photosystems to harvest light energy (Fig 1). Contrary to reaction-center photosystems, proton-pumping rhodopsins cannot regenerate electron donors, so for autotrophic growth they need to be complemented with electron donor uptake mechanisms These electron uptake mechanisms and photosystems could be integrated with a carbon fixation pathway that can be chosen from a variety of (anaerobic) synthetic and natural pathways [20]. The presented, integrated in silico approach allows synthetic biologists and metabolic engineers to better evaluate and compare complex designs for e.g. autotrophy before experimental implementation
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