FEBS Letters
Volume 582, Issue 9 , Pages 1330-1334, 16 April 2008

Promoted evolution of a shortened variant of heme A synthase in the membrane of Bacillus subtilis

Edited by Peter Brzezinski

Department of Cell and Organism Biology, Lund University, Sölvegatan 35, SE 22362 Lund, Sweden

Received 15 February 2008; received in revised form 10 March 2008; accepted 11 March 2008. published online 20 March 2008.

Abstract 

Bacillus subtilis heme A synthase is a membrane protein with 8 transmembrane segments. By using a two-step mutagenesis approach we have generated and selected a fully functional enzyme protein variant with a seven residue internal deletion. The biochemical properties of the shortened variant are similar to those of the normal enzyme. This could indicate that residue H209 in the mutant protein substitutes for the missing H216 as an axial ligand to the heme iron. Our results provide insight in routes of membrane protein evolution and the structure of heme A synthases.

Keywords: CtaA, Heme A synthesis, Membrane protein evolution, Cytochrome a, Bacillus subtilis

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PII: S0014-5793(08)00244-5

doi:10.1016/j.febslet.2008.03.015

FEBS Letters
Volume 582, Issue 9 , Pages 1330-1334, 16 April 2008