% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Battling:873929,
author = {Battling, Svenja and Wohlers, Karen and Igwe, Chika and
Kranz, Angela and Pesch, Matthias and Wirtz, Astrid and
Baumgart, Meike and Büchs, Jochen and Bott, Michael},
title = {{N}ovel plasmid-free {G}luconobacter oxydans strains for
production of the natural sweetener 5-ketofructose},
journal = {Microbial cell factories},
volume = {19},
number = {1},
issn = {1475-2859},
address = {London},
publisher = {Biomed Central},
reportid = {FZJ-2020-01102},
pages = {54},
year = {2020},
note = {Biotechnologie 1},
abstract = {5-Ketofructose (5-KF) has recently been identified as a
promising non-nutritive natural sweetener. Gluconobacter
oxydans strains have been developed that allow efficient
production of 5-KF from fructose by plasmid-based expression
of the fructose dehydrogenase For plasmid-free 5-KF
production, we selected four sites in the genome of G.
oxydans IK003.1 and inserted the fdhSCL genes under control
of the strong P264 promoter into each of these sites. All
four recombinant strains expressed fdhSCL and oxidized
fructose to 5-KF, but site-specific differences were
observed suggesting that the genomic vicinity influenced
gene expression. For further improvement, a second copy of
the fdhSCL genes under control of P264 was inserted into the
second-best insertion site to obtain strain
IK003.1::fdhSCL2. The 5-KF production rate and the 5-KF
yield obtained with this double-integration strain were
considerably higher than for the single integration strains
and approached the values of IK003.1 with plasmid-based
fdhSCL expression.We identified four sites in the genome of
G. oxydans suitable for expression of heterologous genes and
constructed a strain with two genomic copies of the fdhSCL
genes enabling efficient plasmid-free 5-KF production. This
strain will serve as basis for further metabolic engineering
strategies aiming at the use of alternative carbon sources
for 5-KF production and for bioprocess optimization.},
cin = {IBG-1},
ddc = {570},
cid = {I:(DE-Juel1)IBG-1-20101118},
pnm = {581 - Biotechnology (POF3-581)},
pid = {G:(DE-HGF)POF3-581},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32131833},
UT = {WOS:000521169100001},
doi = {10.1186/s12934-020-01310-7},
url = {https://juser.fz-juelich.de/record/873929},
}