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Brandenburg, F.

Publications and source records attributed to Brandenburg, F..

2 recordsLinked to original sources

Multilevel engineering of cyanobacterial energy metabolism advances photosynthetic hydrogen production while revealing its constraints

Hydrogen (H2) is a promising sustainable energy carrier, and its direct production from photosynthetic water splitting is appealing. Yet long-term photosynthetic hydrogen production by cyanobacteria remains inefficient despite decades of engineering. Here, we systematically dissect the hierarchical and state-dependent constraint architecture governing sustained H2 evolution in Synechocystis sp. PCC 6803. We show that hydrogenase overexpression relieves the primary enzymatic limitation, exposing ATP/NADPH balancing and competing electron sinks as successive metabolic constraints. Inspired by cyanophage strategies, we engineered synthetic CP12-based regulatory proteins that redirect photosynthetic electrons from CO2 fixation toward H2 production. Combining these interventions increases H2 production by over two orders of magnitude relative to the previous benchmark system, demonstrating that sustained H2 production requires coordinated management of metabolism and regulation rather than elimination of a single bottleneck. However, overcoming these constraints also promotes metabolic adaptations and genetic instability, illustrating the trade-off between maximal H2 production and long-term metabolic stability.

bioengineering↗

Hemi Manganese Exporters 1 and 2 enable manganese transport at the plasma membrane in cyanobacteria

Manganese (Mn) is key to oxygenic photosynthesis as it catalyzes the splitting of water in photosystem II and functions as cofactor of multiple enzymes. A single ABC-type transporter, MntCAB, is so far established for the uptake of the metal under limiting conditions in cyanobacteria. It is unknown how Mn is imported under replete conditions. We identified two proteins in the cyanobacterium Synechocystis sp. PCC 6803, which are homologous to the unknown protein family 0016 (UPF0016) member manganese exporter (Mnx). In contrast to Mnx, which consists of six transmembrane domains, the new candidate proteins contain three transmembrane domains. Hence, we named them hemi manganese exchangers (Hmx) 1 and 2. Knock-out mutants in hmx1 and/or hmx2 showed sensitivity toward low Mn supplementation, and reduced intracellular Mn pools. Additional deletion of mntC hindered the cells to thrive unless the medium was supplemented with Mn to compensate for the depletion of their intracellular Mn pool. In accordance with the observed localization of Hmx1 and Hmx2 in the plasma membrane, we postulate a Mn uptake function for heteromeric Hmx1/2 across the plasma membrane under a wide range of Mn concentrations and a supporting role for the MntCAB system under Mn-limiting conditions. On the basis of their phylogenies, we propose that Hmx1 and Hmx2 are the ancestral progenitors of eukaryote-type UPF0016 proteins with six transmembrane domains. The Mn transport function of Hmx1/2 underscores this as a fundamental and ancient feature of the UPF0016 family. Potentially, Hmx1 and Hmx2 coevolved with the internalization of the oxygen-evolving complex.

plant biology↗