Exploring the proton pump and exit pathway for pumped protons in cytochrome ba3 from Thermus thermophilus.

Abstract:

:The heme-copper oxygen reductases are redox-driven proton pumps. In the current work, the effects of mutations in a proposed exit pathway for pumped protons are examined in the ba(3)-type oxygen reductase from Thermus thermophilus, leading from the propionates of heme a(3) to the interface between subunits I and II. Recent studies have proposed important roles for His376 and Asp372, both of which are hydrogen-bonded to propionate-A of heme a(3), and for Glu126(II) (subunit II), which is hydrogen-bonded to His376. Based on the current results, His376, Glu126(II), and Asp372 are not essential for either oxidase activity or proton pumping. In addition, Tyr133, which is hydrogen-bonded to propionate-D of heme a(3), was also shown not to be essential for function. However, two mutations of the residues hydrogen-bonded to propionate-A, Asp372Ile and His376Asn, retain high electron transfer activity and normal spectral features but, in different preparations, either do not pump protons or exhibit substantially diminished proton pumping. It is concluded that either propionate-A of heme a(3) or possibly the cluster of groups centered about the conserved water molecule that hydrogen-bonds to both propionates-A and -D of heme a(3) is a good candidate to be the proton loading site.

authors

Chang HY,Choi SK,Vakkasoglu AS,Chen Y,Hemp J,Fee JA,Gennis RB

doi

10.1073/pnas.1107345109

subject

Has Abstract

pub_date

2012-04-03 00:00:00

pages

5259-64

issue

14

eissn

0027-8424

issn

1091-6490

pii

1107345109

journal_volume

109

pub_type

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