Rational design of DAHP synthase and prephenate dehydrogenase for metabolic engineering of Bacillus amyloliquefaciens to produce L-tyrosine
International Journal of Biological Macromolecules,
Год журнала:
2025,
Номер
307, С. 142076 - 142076
Опубликована: Март 15, 2025
Язык: Английский
Functional analysis of tandem glycosyltransferases catalyzing the O-glycosylation of flavonoid 4'-O-glycosyl-6-C-glycosides biosynthesis from Isatis indigotica
Plant Physiology and Biochemistry,
Год журнала:
2025,
Номер
unknown, С. 109920 - 109920
Опубликована: Апрель 1, 2025
Язык: Английский
Advances and Challenges in Biomanufacturing of Glycosylation of Natural Products
Shunyang Hu,
Bangxu Wang,
Liang Pei
и другие.
Fermentation,
Год журнала:
2024,
Номер
10(7), С. 349 - 349
Опубликована: Июль 9, 2024
Glycosylation
is
one
of
the
most
common
and
important
modifications
in
natural
products
(NPs),
which
can
alter
biological
activities
properties
NPs,
effectively
increase
structural
diversity,
improve
pharmacological
activities.
The
biosynthesis
glycosylation
involves
multiple
complex
processes,
are
coordinated
by
many
enzymes.
UDP-glycosyltransferases
(UGTs)
play
a
crucial
role
modification,
have
attracted
long-term
widespread
research
attention.
UGTs
catalyze
O-,
C-,
S-,
N-glycosylation
different
substrates,
producing
variety
glycosides
with
broad
activity,
while
improving
solubility,
stability,
bioavailability,
other
functions
NPs.
In
recent
years,
rapid
development
synthetic
biology
advanced
manufacturing
technologies,
especially
application
artificial
intelligence
field
biology,
has
led
to
series
new
discoveries
NP
UGT.
This
work
summarizes
latest
progress
challenges
glycosylation,
covering
results
potential
applications
glycosylated
derivatives
terpenes,
flavonoids,
polyphenols,
aromatic
compounds,
compounds
terms
biogenesis.
Looking
future,
may
leverage
intelligence-driven
techniques
decipher
genes
related
pathway,
expected
further
promote
large-scale
synthesis
diversity
NPs
pharmaceutical,
functional
food,
cosmetic
industries.
Язык: Английский
Insights into functional divergence, catalytic versatility and specificity of small molecule glycosyltransferases
International Journal of Biological Macromolecules,
Год журнала:
2024,
Номер
unknown, С. 138821 - 138821
Опубликована: Дек. 1, 2024
Язык: Английский
Multi-strategy integration improves 28-O-glucosylation of asiatic acid into asiatic acid monoglucoside
Food Bioscience,
Год журнала:
2024,
Номер
61, С. 104832 - 104832
Опубликована: Июль 27, 2024
Язык: Английский
Mining and Engineering the Di-O-glycosylation Pattern of UGT72B1 for the Highly Efficient O-Glycosylation of Endogenous Quercetin
Journal of Agricultural and Food Chemistry,
Год журнала:
2024,
Номер
72(45), С. 25219 - 25228
Опубликована: Окт. 30, 2024
Compared
with
mono-O-glycosylation,
di-O-glycosylation
endows
the
precursor
better
performance.
However,
mining
and
engineering
of
patterns
glycosyltransferases
are
limited,
hindering
their
synthetic
applications.
Here,
an
Arabidopsis
xenobiotic-transforming
glycosyltransferase,
UGT72B1,
was
found
to
catalyze
glycosylation
endogenous
quercetin
its
monoglycosides,
generating
di-O-glucosides.
Mutating
M17/G18/Y315
into
L/T/Q
in
UGT72B1
altered
regioselectivity
toward
7-O-glucoside,
enzymatically
another
3,7-di-O-glycoside
up
a
100%
conversion
rate,
increased
sugar
donor
preference.
Altering
regiospecificity
likely
required
coordination
between
entrance
active
site,
where
orientations
acceptors
donors
shift
adopt
lower
binding
energy
state.
Moreover,
3,4′-di-O-β-d-glucoside
3,7-di-O-β-d-glucoside
synthesized
were
have
highest
anti-inflammatory
activities.
Overall,
this
work
presents
efficient
strategy
engineer
for
synthesis
di-O-β-d-glucosides
be
used
as
food
additives,
therapeutics,
nutraceuticals.
Язык: Английский
Engineering Escherichia coli for Efficient De Novo Synthesis of Salidroside
Journal of Agricultural and Food Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 12, 2024
Salidroside
is
a
high-value
plant-derived
glycoside
with
diverse
biological
activities,
but
the
main
industrial
salidroside
production
method,
extraction
from
Язык: Английский