Species differences in unlocking B-side electron transfer in bacterial reaction centers

  • Nicholas P. Dylla
  • , Kaitlyn M. Faries
  • , Ryan M. Wyllie
  • , Angela M. Swenson
  • , Deborah K. Hanson
  • , Dewey Holten
  • , Christine Kirmaier
  • , Philip D. Laible

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)2515-2526
Number of pages12
JournalFEBS Letters
DOIs
StatePublished - Aug 1 2016

Keywords

  • charge separation
  • high-throughput mutagenesis
  • photosynthetic bacteria
  • rapid screening
  • time-resolved spectroscopy

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