Abstract
The structure of the bacterial photosynthetic reaction center (RC) reveals symmetry-related electron transfer (ET) pathways, but only one path is used in native RCs. Analogous mutations have been made in two Rhodobacter (R.) species. A glutamic acid at position 133 in the M subunit increases transmembrane charge separation via the naturally inactive (B-side) path through impacts on primary ET in mutant R. sphaeroidesRCs. Prior work showed that the analogous substitution in the R. capsulatusRC also increases B-side activity, but mainly affects secondary ET. The overall yields of transmembrane ET are similar, but enabled in fundamentally different ways.
| Original language | English |
|---|---|
| Pages (from-to) | 2515-2526 |
| Number of pages | 12 |
| Journal | FEBS Letters |
| DOIs | |
| State | Published - Aug 1 2016 |
Keywords
- charge separation
- high-throughput mutagenesis
- photosynthetic bacteria
- rapid screening
- time-resolved spectroscopy
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