1. Functional reconstitution of a bacterial CO2 concentrating mechanism in Escherichia coli
- Author
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David F. Savage, Shira Amram, Cecilia Blikstad, Ron Milo, Arren Bar-Even, Avi I. Flamholz, Eli J Dugan, Shmuel Gleizer, Niv Antonovsky, Sumedha Ravishankar, Elad Noor, and Roee Ben-Nissan
- Subjects
0106 biological sciences ,0301 basic medicine ,QH301-705.5 ,Science ,Chemical biology ,Photosynthesis ,medicine.disease_cause ,carboxysome ,01 natural sciences ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,Synthetic biology ,medicine ,Biology (General) ,Escherichia coli ,photosynthesis ,General Immunology and Microbiology ,biology ,Chemistry ,General Neuroscience ,Carbon fixation ,RuBisCO ,General Medicine ,co2 concentrating mechanism ,biology.organism_classification ,co2 fixation ,Cell biology ,Carboxysome ,030104 developmental biology ,biology.protein ,Medicine ,synthetic biology ,Bacteria ,010606 plant biology & botany - Abstract
Many photosynthetic organisms employ a CO2concentrating mechanism (CCM) to increase the rate of CO2fixation via the Calvin cycle. CCMs catalyze โ50% of global photosynthesis, yet it remains unclear which genes and proteins are required to produce this complex adaptation. We describe the construction of a functional CCM in a non-native host, achieved by expressing genes from an autotrophic bacterium in anEscherichia colistrain engineered to depend on rubisco carboxylation for growth. Expression of 20 CCM genes enabledE. colito grow by fixing CO2from ambient air into biomass, with growth in ambient air depending on the components of the CCM. Bacterial CCMs are therefore genetically compact and readily transplanted, rationalizing their presence in diverse bacteria. Reconstitution enabled genetic experiments refining our understanding of the CCM, thereby laying the groundwork for deeper study and engineering of the cell biology supporting CO2assimilation in diverse organisms.
- Published
- 2020
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