Affiliation:
1. Department of Biochemistry, University of Connecticut Health Center, Farmington, Connecticut 06032
Abstract
ABSTRACT
Variants of the wild-type
Bacillus subtilis
α/β-type small, acid-soluble spore protein (SASP) SspC
wt
were designed to evaluate the contribution of C-terminal residues to these proteins' affinity for DNA. SspC variants lacking one to three C-terminal residues were similar to SspC
wt
in DNA binding, but removal of six C-terminal residues greatly decreased DNA binding. In contrast, a C-terminal extension of three residues increased SspC's affinity for DNA 5- to 10-fold. C-terminal and N-terminal changes that independently caused large increases in SspC-DNA binding affinity were combined and produced an additive effect on DNA binding; the affinity of the resulting variant, SspC
ΔN11-D13K-C3
, for DNA was increased ≥20-fold over that of SspC
wt
. For most of the SspC variants tested, lowering the pH from 7 to 6 improved DNA binding two- to sixfold, although the opposite effect was observed with variants having additional C-terminal basic residues. In vitro, the binding of SspC
ΔN11-D13K-C3
to DNA suppressed the formation of cyclobutane-type thymine dimers and promoted the formation of the spore photoproduct upon UV irradiation to the same degree as the binding of SspC
wt
. However,
B. subtilis
spores lacking major α/β-type SASP and overexpressing SspC
ΔN11-D13K-C3
had a 10-fold-lower viability and far less UV and heat resistance than spores overexpressing SspC
wt
. This apparent lack of DNA protection by SspC
ΔN11-D13K-C3
in vivo is likely due to the twofold-lower level of this protein in spores compared to the level of SspC
wt
, perhaps because of effects of SspC
ΔN11-D13K-C3
on gene expression in the forespore during sporulation. The latter results indicate that only moderately strong binding of α/β-type SASP to DNA is important to balance the potentially conflicting requirements for these proteins in DNA transcription and DNA protection during spore formation, spore dormancy, and spore germination and outgrowth.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
12 articles.
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