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Kosmützky, D.

Publications and source records attributed to Kosmützky, D..

3 recordsLinked to original sources

Dissecting a biological electron transport network with electrochemistry

Photosynthetic membranes contain complex networks of redox proteins and molecules which direct electrons along various energy-to-chemical interconversion reactions important for sustaining life on Earth. Analysing and disentangling the mechanisms, regulation and interdependencies of these electron transfer pathways is extremely difficult, owing to the large number of interacting components in the native membrane environment. Whilst electrochemistry is well established for studying electron transfer in purified proteins, it has proven difficult to directly wire into proteins within their native membrane environments, and even harder to probe on a systems-level the electron transfer networks they are entangled within. Here, we show how photosynthetic membranes from cyanobacteria can be directly wired to electrodes to access their complex electron transfer networks. Measurements of native membranes with structured electrodes revealed distinctive electrochemical signatures, enabling analysis from the scale of individual proteins to entire biochemical pathways, as well as their interplay. This includes measurements of overlapping photosynthetic and respiratory pathways, the redox activities of membrane-bound quinones, along with validation using in operando spectroscopic measurements. Importantly, we further demonstrated direct extraction of electrons from native membrane-bound Photosystem I at -600 mV, which is [~]1 V more negative than from purified photosystems. This finding opens up opportunities for biotechnologies for solar electricity, fuel and chemical generation. We foresee this electrochemical method being adapted to analyze other photosynthetic and non-photosynthetic membranes, as well as aiding the development of new biocatalytic, biohybrid and biomimetic systems.

biochemistry↗

Establishment of a novel set of vectors for transformation of the dinoflagellate Amphidinium carterae

Peridinin-containing dinoflagellate algae have a chloroplast genome formed from plasmid-like minicircles. This fragmented genome has allowed us to develop a genetic modification methodology involving the use of biolistics to introduce artificial minicircles in Amphidinium carterae (Nimmo et al., 2019). The previously reported artificial minicircles were based on native minicircles containing either the psbA or atpB gene. Each artificial minicircle allowed expression of a single selectable marker instead of psbA or atpB. Here, we present two further artificial minicircles for use in transformation of A. carterae. One is based on the petD minicircle, allowing the expression of a single selectable marker. The second is based on the two-gene minicircle originally containing atpA and petB, and allows the dual expression of a selectable marker and a gene of interest. Our research suggest that all of the 20 or so minicircles in A. carterae are suitable for adaptation as artificial minicircles, allowing for the simultaneous introduction of multiple genes.

plant biology↗

The evolution of the cytochrome c6 family of photosynthetic electron transfer proteins

During photosynthesis, electrons are transferred between the cytochrome b6f complex and photosystem I. This is carried out by the protein plastocyanin in plant chloroplasts. In contrast, electron transfer can be carried out by either plastocyanin or cytochrome c6 in many cyanobacteria and eukaryotic algal species. There are three further cytochrome c6 homologues: cytochrome c6A in plants and green algae, and cytochromes c6B and c6C in cyanobacteria. The function of these proteins is unknown. Here, we present a comprehensive analysis of the evolutionary relationship between the members of the cytochrome c6 family in photosynthetic organisms. Our phylogenetic analyses show that cytochrome c6B and cytochrome c6C are likely to be orthologues that arose from a duplication of cytochrome c6, but that there is no evidence for separate origins for cytochrome c6B and c6C. We therefore propose re-naming cytochrome c6C as cytochrome c6B. We show that cytochrome c6A is likely to have arisen from cytochrome c6B rather than by an independent duplication of cytochrome c6, and present evidence for an independent origin of a protein with some of the features of cytochrome c6A in peridinin dinoflagellates. We conclude with a new comprehensive model of the evolution of the cytochrome c6 family which is an integral part of understanding the function of the enigmatic cytochrome c6 homologues.

evolutionary biology↗