Cyclization diversity of meroditerpenoids from endophytic fungi of medicinal plants driven by synthetic biology strategies
Science of Traditional Chinese Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 24, 2025
Abstract
Background
Medicinal
plants
rich
in
endophytic
fungi
are
a
significant
source
of
natural
lead
compounds.
Meroterpenoids,
which
hybrid
products
originating
from
partially
terpenoid
pathways,
exhibit
impressive
structural
complexity
and
substantial
potential
as
drug
candidates.
The
diversity
meroterpenoids
is
largely
attributed
to
the
functional
cyclases,
generate
variety
compounds
with
different
ring
systems.
This
enzymatic
versatility
underscores
biochemical
their
invaluable
role
discovery.
Objective
aim
study
was
investigate
Paris
polyphylla
var.
yunnanensis
facilitating
diverse
cyclization
modifications
meroditerpenoids
through
four
terpene
cyclases
(TCs)
Pyr4
family.
Methods
utilized
recombinant
strategy
successfully
reconstruct
distinct
TCs
heterologous
host,
Aspergillus
oryzae
NSAR1.
characterization
resulting
secondary
metabolites
performed
using
mass
spectrometry
NMR
techniques.
Results
substitution
endophytes
felis
0260
Fusarium
graminearum
1962
hydrophobic
intermediates
1
2
,
led
production
sartorypyrone
C
(
3
)
new
compound,
4′-methylchevalone
E
4
),
respectively.
demonstrates
critical
enhancing
diversity.
Conclusions
These
findings
provide
valuable
insights
into
compatibility
pathway
combinations
interchangeability
derived
medicinal
plants,
advanced
understanding
meroditerpenoid
biosynthesis
highlighted
importance
Language: Английский
Formation of N-Hydroxyethylisoindolinone Derivatives in Fungi Requires Highly Coordinated Consecutive Oxidation Steps
LI Zhang-hai,
No information about this author
Yu Dai,
No information about this author
Jing Zhou
No information about this author
et al.
Organic Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Gene
duplication
significantly
contributes
to
the
diversification
of
biosynthetic
potential
and
increases
structural
diversity
secondary
metabolites.
Here,
we
report
second
alkyl
salicylaldehyde
derivative
gene
cluster
in
Penicillium
roqueforti,
being
responsible
for
formation
ethanolamine-containing
derivatives.
Heterologous
expression
feeding
experiments
provided
evidence
their
via
collaboration
modification
with
one
cytochrome
P450
two
flavin-containing
monooxygenases
a
highly
ordered
manner
before
after
ethanolamine
incorporation.
Language: Английский
DMSO enhances the biosynthesis of epoxyquinols in Pestalotiopsis sp. (strain IQ-011) and yields new [4 + 2] cycloaddition dimers
Organic & Biomolecular Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
DMSO-induced
epigenetic
modulation
of
Pestalotiopsis
sp.
IQ-011,
and
combined
with
metabolomic
analysis,
led
to
the
discovery
four
novel
metabolites,
including
three
dimeric
epoxyquinols
generated
via
[4
+
2]
cycloaddition.
Language: Английский
Cupin-domain containing protein is not essential for the alkyl salicylaldehyde formation in Aspergillus ustus
Marlies Peter,
No information about this author
Shu‐Ming Li
No information about this author
Chemical Communications,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
Previous
studies
demonstrated
the
requirement
of
four
enzymes
including
a
cupin-domain
containing
protein
for
formation
alkyl
salicylaldehydes
and
derivatives.
Heterologous
expression
three
biosynthetic
genes
from
Language: Английский