Allantofuranone Biosynthesis and Precursor-Directed Mutasynthesis of Hydroxylated Analogues
Carsten Wieder,
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Claudia Simon-Sánchez,
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Johannes C. Liermann
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et al.
Journal of Natural Products,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 18, 2025
Genome
mining
and
heterologous
reconstitution
of
biosynthetic
genes
in
Aspergillus
oryzae
enabled
elucidation
the
hitherto
elusive
route
that
produces
allantofuranone
(1),
a
bioactive
natural
product
originally
isolated
from
Allantophomopsis
lycopodina.
The
core
non-ribosomal
peptide
synthetase
(NRPS)-like
enzyme
AlfA
alf
BGC
polyporic
acid
(2)
phenylpyruvic
acid.
In
subsequent
reactions,
compound
2
is
reductively
dehydrated
by
bifunctional
AlfC
methylated
AlfD
to
produce
terferol
(6).
final
step,
quinol
moiety
6
oxidatively
cleaved
contracted
aromatic
ring
cleavage
dioxygenase
AlfB.
Using
combinatorial
biosynthesis,
we
were
able
manipulate
yield
hydroxylated
pathway
congeners,
most
notably
new
products
deoxyascocorynin
(10),
hydroxyterferol
(11),
hydroxyallantofuranone
(12).
Language: Английский
Hot off the Press
Natural Product Reports,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
A
personal
selection
of
32
recent
papers
is
presented
covering
various
aspects
current
developments
in
bioorganic
chemistry
and
novel
natural
products
such
as
melichuniione
from
Melicope
chunii.
Language: Английский