Abstract

Cyanobacteria are versatile unicellular phototrophic microorganisms that are highly abundant in many environments. Owing to their capability to utilize solar energy and atmospheric carbon dioxide for growth, cyanobacteria are increasingly recognized as a prolific resource for the synthesis of valuable chemicals and various biofuels. To fully harness the metabolic capabilities of cyanobacteria necessitates an in-depth understanding of the metabolic interconversions taking place during phototrophic growth, as provided by genome-scale reconstructions of microbial organisms. Here we present an extended reconstruction and analysis of the metabolic network of the unicellular cyanobacterium Synechocystis sp. PCC 6803. Building upon several recent reconstructions of cyanobacterial metabolism, unclear reaction steps are experimentally validated and the functional consequences of unknown or dissenting pathway topologies are discussed. The updated model integrates novel results with respect to the cyanobacterial TCA cycle, an alleged glyoxylate shunt, and the role of photorespiration in cellular growth. Going beyond conventional flux-balance analysis, we extend the computational analysis to diurnal light/dark cycles of cyanobacterial metabolism.

Highlights

  • Almost all life on Earth depends on oxygenic photosynthesis to capture solar energy and convert atmospheric carbon into organic compounds that serve as nutrients for heterotrophic organisms

  • To harness solar energy using cyanobacteria often requires targeted modifications of the metabolic network – a task that would greatly benefit from an indepth understanding of metabolic interconversions taking place during phototrophic growth

  • The manuscript is organized as follows: First, we provide a brief overview on the current status of our reconstruction of the metabolic network of the cyanobacterium Synechocystis sp

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Summary

Introduction

Almost all life on Earth depends on oxygenic photosynthesis to capture solar energy and convert atmospheric carbon into organic compounds that serve as nutrients for heterotrophic organisms. A first step towards such an increased understanding is often provided by detailed and validated genomescale reconstructions of the metabolic networks of the respective organisms. PCC 6803, became available [10,11,12,13,14,15,16,17,18] While these reconstructions differ significantly in reliability, size and scope, each led too useful insight into the metabolic organization of the model organism. Analysis of different reconstructions allows us to pinpoint open questions in the representation of the metabolic network of Synechocystis sp. The updated model integrates novel results with respect to the cyanobacterial TCA cycle, an alleged glyoxylate shunt, the role of photorespiration in cellular growth, as well peculiarities of photosynthetic reactions such as light-dependent oxidative stress. We seek to improve the applicability of FBA on phototrophic conditions by implementing a full diurnal

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