Polyethylene and related hydrocarbon polymers (“plastics”) are not biodegradable
New Biotechnology,
Journal Year:
2024,
Volume and Issue:
83, P. 231 - 238
Published: Aug. 24, 2024
Research
on
the
biodegradation
of
polyethylene
(PE),
polystyrene
(PS)
and
related
polymers
has
become
popular
number
publications
this
topic
is
rapidly
increasing.
However,
there
no
convincing
evidence
that
frequently
claimed
biodegradability
these
so-called
"plastics"
really
exists.
Rather,
a
diffuse
definition
term
"biodegradability"
led
to
publication
reports
showing
either
marginal
weight
losses
hydrocarbon
by
action
isolated
bacterial
strains
or
mechanical
disintegration
polymer
surface
modification
in
case
polymer-consuming
insect
larvae.
Most
data
can
be
alternatively
explained
utilization
impurities/additives,
low
molecular
oligomers,
and/or
physical
fragmentation
subsequent
loss
small
fragments.
Evidence
for
(partial)
biotic
abiotic
oxidation
amorphous
fraction
surface-exposed
side
chains
not
sufficient
claim
PE
biodegradable.
To
best
my
knowledge,
report
been
so
far
published
which
substantial
mineralization
(long
chain
length)
carbon
dioxide
convincingly
demonstrated
determination
fate
atoms
isotope-labeled
polymers.
It
disappointing
with
critical
view
are
cited
most
reports.
The
possibility
should
considered
expanding
research
field
chasing
rainbows.
Language: Английский
Nature-Inspired Strategies for Sustainable Degradation of Synthetic Plastics
JACS Au,
Journal Year:
2024,
Volume and Issue:
4(9), P. 3323 - 3339
Published: Aug. 27, 2024
Synthetic
plastics
have
become
integral
to
our
daily
lives,
yet
their
escalating
production,
limited
biodegradability,
and
inadequate
waste
management
contribute
environmental
contamination.
Biological
plastic
degradation
is
one
promising
strategy
address
this
pollution.
The
inherent
chemical
physical
properties
of
synthetic
plastics,
however,
pose
challenges
for
microbial
enzymes,
hindering
the
effective
development
a
sustainable
biological
recycling
process.
This
Perspective
explores
alternative,
nature-inspired
strategies
designed
overcome
some
key
limitations
in
currently
available
plastic-degrading
enzymes.
Nature's
refined
pathways
natural
polymers,
such
as
cellulose,
present
compelling
framework
efficient
technologies
enzymatic
degradation.
By
drawing
insights
from
nature,
we
propose
general
employing
substrate
binding
domains
improve
targeting
multienzyme
scaffolds
efficiency
limitations.
As
potential
application,
outline
pathway
upcycle
polyethylene
into
alkenes.
Employing
can
path
toward
solution
impact
plastics.
Language: Английский
Design of Plastic Binding Lytic Polysaccharide Monooxygenases via Modular Engineering
Alessia Munzone,
No information about this author
Manon Pujol,
No information about this author
Majda Badjoudj
No information about this author
et al.
Chem & Bio Engineering,
Journal Year:
2024,
Volume and Issue:
1(10), P. 863 - 875
Published: Sept. 27, 2024
The
worldwide
accumulation
of
plastic
waste
in
the
environment,
along
with
its
lifespan
hundreds
years,
represents
a
serious
threat
to
ecosystems.
Enzymatic
recycling
offers
promising
solution,
but
high
chemical
inertness
and
hydrophobicity
plastics
pose
several
challenges
enzymes.
In
nature,
lytic
polysaccharide
monooxygenases
(LPMOs)
can
act
at
surface
recalcitrant
biopolymers,
taking
advantage
their
solvent-exposed
active
sites
appended
carbohydrate-binding
modules
(CBMs).
LPMOs
disrupt
densely
packed
chains
polysaccharides
(e.g.,
cellulose)
by
oxidation
C-H
bonds.
Given
similarities
between
these
natural
artificial
polymers,
we
aimed
here
promoting
plastic-binding
properties
LPMOs,
swapping
CBM
three
natural,
surface-active
accessory
displaying
different
amphipathic
properties.
polymer
binding
capacity
resulting
LPMO
chimeras
was
assessed
on
library
synthetic
including
polyester,
polyamide,
polyolefin
substrates.
We
demonstrated
that
engineered
are
polymer-dependent
be
tuned
playing
nature
module
reaction
conditions.
Remarkably,
gained
full
for
some
chimera
striking
results
polyhydroxyalkanoates
(PHA).
long
term
perspective
harnessing
unique
copper
chemistry
degrade
plastics,
also
provided
first
evidence
LPMO-dependent
modification
PHA
polymer,
as
supported
enzyme
assays,
gel
permeation
chromatography,
scanning
electron
microscopy.
Altogether,
our
study
provides
roadmap
engineering
ability
constituting
crucial
step
evolutionary
path
toward
efficient
interfacial
catalysis
plastic-active
Language: Английский