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@ARTICLE{Rebets:858501,
author = {Rebets, Yuriy and Tsolis, Konstantinos C. and
Guðmundsdóttir, Elísabet Eik and Koepff, Joachim and
Wawiernia, Beata and Busche, Tobias and Bleidt, Arne and
Horbal, Liliya and Myronovskyi, Maksym and Ahmed, Yousra and
Wiechert, Wolfgang and Rückert, Christian and Hamed,
Mohamed B. and Bilyk, Bohdan and Anné, Jozef and
Friðjónsson, Ólafur and Kalinowski, Jörn and Oldiges,
Marco and Economou, Anastassios and Luzhetskyy, Andriy},
title = {{C}haracterization of {S}igma {F}actor {G}enes in
{S}treptomyces lividans {TK}24 {U}sing a {G}enomic
{L}ibrary-{B}ased {A}pproach for {M}ultiple {G}ene
{D}eletions},
journal = {Frontiers in microbiology},
volume = {9},
issn = {1664-302X},
address = {Lausanne},
publisher = {Frontiers Media},
reportid = {FZJ-2018-07372},
pages = {3033},
year = {2018},
abstract = {Alternative sigma factors control numerous aspects of
bacterial life, including adaptation to physiological
stresses, morphological development, persistence states and
virulence. This is especially true for the physiologically
complex actinobacteria. Here we report the development of a
robust gene deletions system for Streptomyces lividans TK24
based on a BAC library combined with the λ-Red
recombination technique. The developed system was validated
by systematically deleting the most highly expressed genes
encoding alternative sigma factors and several other
regulatory genes within the chromosome of S. lividans TK24.
To demonstrate the possibility of large scale genomic
manipulations, the major part of the undecylprodigiosin gene
cluster was deleted as well. The resulting mutant strains
were characterized in terms of morphology, growth
parameters, secondary metabolites production and response to
thiol-oxidation and cell-wall stresses. Deletion of
$SLIV_12645$ gene encoding S. coelicolor SigR1 ortholog has
the most prominent phenotypic effect, resulted in
overproduction of actinorhodin and coelichelin P1 and
increased sensitivity to diamide. The secreted proteome
analysis of $SLIV_12645$ mutant revealed SigR1 influence on
trafficking of proteins involved in cell wall biogenesis and
refactoring. The reported here gene deletion system will
further facilitate work on S. lividans strain improvement as
a host for either secondary metabolites or protein
production and will contribute to basic research in
streptomycetes physiology, morphological development,
secondary metabolism. On the other hand, the systematic
deletion of sigma factors encoding genes demonstrates the
complexity and conservation of regulatory processes
conducted by sigma factors in streptomycetes.},
cin = {IBT-1},
ddc = {570},
cid = {I:(DE-Juel1)VDB55},
pnm = {581 - Biotechnology (POF3-581)},
pid = {G:(DE-HGF)POF3-581},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000452616600001},
doi = {10.3389/fmicb.2018.03033},
url = {https://juser.fz-juelich.de/record/858501},
}