Sr. No. |
Title of the paper |
Type of the polythene used |
Techniques used to
assess polythene
degradation |
Source of the
microbes used |
Major findings/
conclusions/inferences |
Level of
Identification |
Name of the microbes /
enzymes responsible |
Reference |
1. |
Assessment of the
biodegradation of
polythene |
Polythene carry
bags |
Percentage of
weight, surface
corrosion, tensile
strength |
Plastic dumping
sites |
After 3 months of regular
shaking the polythene
discs were corroded on
the surface and tensile
strength decreases and
maximum 12.5% weight
loss was recorded. |
Morphological
keys and
Biochemical
tests |
Bacillius cerues and
Psedomonas sp. |
[56] |
2. |
Biodegradation of
degradable plastic
polyethylene by
Phanerochaete
and Streptomyces
species |
degradable
plastic contained
pro-oxidant and
6% starch |
Weight loss,
changes in tensile
strength, percent
elongation and
molecular weight
distribution |
The lignocellulose
degrading
microorganisms
(not specified the
site of collection) |
50% reduction
in tensile strength (S.
viridosporus T7A). |
Not specified |
Streptomyces viridosporus
T7A, S. badius 252, and
S. setonii 75Vi2 (bacteria)
and Phanerochaete
chrysosporium
(fungus) |
[4] |
3. |
Biodegradability
of polythene and
plastic by the help
of microorganism:
a way for brighter
future |
Polythene bags
and plastic cups |
Weight loss |
Five sources:
Medicinal Garden
soil, (B) Sewage
Water Soil, (C)
Energy Park
soil, (D) Sludge
Area soil, (E)
Agricultural
Soil |
After one month of
incubation in both
bacterial and fungal
isolates the maximum
degradation by fungi
(Aspergillus niger) and
bacteria (Streptococcus
lactis) was found as
12.25% and 12.5 %
respectively |
Morphological
keys and
biochemical
tests |
B1(Pseudomonas),
B2(Bacillus subtilis),
B3(Staphylococcus
aureus), B4(Streptococcus
lactis), B5(Proteus
vulgaris),B6 (Micrococcus
luteus), F1(Aspergillus
niger), F2(Aspergillus
nidulance),
F3(Aspergillus
flavus), F4 (Aspergillus
glaucus), F5(Penicillium) |
[57] |
4. |
Biodegradation of
polyethylene by
the thermophilic
bacterium
Brevibacillus
borstelensis. |
Branched
low-density
(0.92 g cm−3)
polyethylene |
Gravimetric and
molecular weight
loss, FTIR |
Soil |
11% (gravimetric) and
30% (molecular) weights
loss was reported at 50°C
after 30 days |
Molecular level
(Using 16S
rDNA) |
Brevibaccillus borstelensis
strain 707 |
[58] |
5. |
Biodegradability
of polyethylene
starch blends
in sea water |
Pure
polyethylene
(5% starch)
and modified
polyethylene
films (8% starch)
and polyethylene
with prodegradant
additives (master
batch in amount
of 20%) |
Changes in weight,
tensile strength
and morphology of
polymer |
Microbes of the
Baltic sea as the
incubation of
polymer samples
was carried out in
Baltic Sea water |
For polyethylene blends
in the sea water very little
microbial degradation
was
observed in winter
but in summer months
the weight loss of
polyethylene with the MB
additive after 20 months
reached 26% |
Not specified |
Not applicable |
[29] |
6. |
Biodegradation
of low density
polyethylene
(LDPE) by fungi
isolated from
marine water– a
SEM analysis |
LPDE in the
powdered form |
Sturm test where
the degradation
was attributed to the
amount of carbon
dioxide evolved and
SEM analysis. |
Sea water |
Per week maximum
4.1594 g/L of CO2
was released after
degradation of the
polythene |
Morphological
keys |
Aspergillus versicolor and
Aspergillus sp. |
[51] |
7. |
Biodegradation
of low density
polythene (LDPE)
by
Pseudomonas
species |
LDPE films |
Weight
measurements,
tensile strength
testing, FTIR-ATR
spectrophotometer
analyses, Scanning
Electron Microscope
based analyses and
GC-MS analyses. |
Known cultures
but source was
not specified |
The highest level of
polythene degradation
(weight loss) out of the
four bacteria was found
as
20% by Pseudomonas
aeruoginosa after 120
days |
Not applicable |
Pseudomonas
aeruginosa PAO1 (ATCC
15729), Pseudomonas
aeruginosa
(ATCC 15692), Pseudomonas
putida (KT2440 ATCC
47054) and Pseudomonas
syringae (DC3000 ATCC
10862) |
[55] |
8. |
Biodegradation of
maleated linear
low-density
polyethylene and
starch blends |
linear lowdensity
polyethylene
torque blended
with starch |
FTIR spectroscopy,
weight loss, SEM,
DSC, TGA. |
Source of the
microbes not
specified but
known cultures
were used |
The starch content in the
blend was found directly
proportional to the he
rate of degradation. Thus,
higher the content of
starch, higher will be the
degree of degradation. |
Not applicable |
Aspergillus niger,
Penicilliurn funiculosum,
Chaetomium globosum,
Gliocladiurn virens and
Pullularia pullulans |
[59] |
9. |
Biodegradation of
photo-degraded
mulching films
based on
polyethylenes
and stearates of
calcium and iron
as pro-oxidant
additives |
LDPE and
LLDPE |
Chemiluminescence,
ATR-FTIR and GCproduct
analysis |
Polythene films
were scattered
in agricultural
vegetable field
and after 30 days
were used for
the isolation of
microbes |
Polythene films 75-85%
(containing Fe stearate)
and 31-67% ( containing
Ca
stearate) at 45°C leads
to reduction in carbonyl
index |
Molecular
level (16S
rRNA gene
sequencing) |
Bacillus cereus, B.
megaterium, B. subtilis and
Brevibacillus borstelensis |
[53] |
10. |
Biofilm
development of
the polyethylenedegrading
bacterium
Rhodococcus
ruber |
Branched
low-density
(0.92 g cm−3)
polyethylene
with an average
molecular
weight of
191,000 |
Weight loss,
SEM analysis
and formation of
extracellular protein
and polysaccharide
in
biofilm of R. ruber
strain C208 on
polyethylene |
Not specified |
7.5% of polythene weight
loss after eight weeks |
Not specified |
Rhodococcus ruber
(C208) |
[54] |
11. |
Colonization,
biofilm formation
and biodegradation
of polyethylene
by a strain of
Rhodococcus
ruber |
Branched
low-density
(0.92 g cm−3)
polyethylene |
Average Weight loss,
Scanning electron
microscopy
ATR and FTIR |
15 sites at which
polyethylene
waste from
agricultural use
(mainly films for
soil mulching) had
been buried |
8% of polyethylene
degradation in 4 weeks |
Molecular level
(16S rDNA
sequencing) |
Rhodococcus ruber C208 |
[60] |
12. |
Comparison of the
biodegradability
of various
polyethylene
films containing
prooxidant
additives |
HDPE, LDPE
and LLDPE with
a balanced
content of
antioxidants and
pro-oxidants |
FTIR, SEC
measurements, H
NMR
spectroscopy and
SEM |
American Type
Culture |
They concluded that the
biodegradation is mainly
controlled by nature of
the pro-oxidant additive
and to a lesser extent
that of
the matrix |
Known microbe
was used |
Rhodococcus rhodochrous
ATCC 29672 |
[61] |
13. |
Degradation
assessment
of low density
polythene (LDP)
and polythene
(PP) by an
indigenous isolates
of Pseudomonas
stutzeri |
Low density
polythene and
polythene |
Tensile strength,
elongation and
percent of extension |
Plastics and soil
from the plastic
dumping site |
After 45 days maximum
change in percent
extension (73.38%
reduction), tensile
strength (0.01 N/cm2 and
it was similar even after
15 and 30 days) and
elongation (1.8cm) of the
polythene was recorded |
Morphological
keys and
biochemical
tests |
Pseudomonas stutzeri |
[62] |
14. |
Diversity and
effectiveness of
tropical mangrove
soil microflora on
the degradation
of polythene carry
bags |
HDPE and LDPE |
Mean weight |
Mangrove soil
sample from
Suva, Fiji Islands |
Nearly 5 % of weight loss
after a period of
eight weeks |
Morphological
keys and
biochemical
tests |
Bacillus,
Micrococcus,
Listeria and
Vibrio |
[63] |
15. |
Diversity of
cellulolytic
microbes and the
biodegradation of
municipal solid
waste by a
potential strain |
Municipal solid
waste |
Weight loss and
cellulose enzyme
production |
Municipal solid
waste, soil and
compost |
With the potential strain
(Trichoderma
viride ) out of the 250
isolates (49 cellulolytic)
after 60 days,
the average weight loss
was 20.10% in the plates
and 33.35% in the piles |
Morphological
keys and
biochemical
tests |
Total 250 isolates (165
belongs to fungi and 85
bacteria) |
[64] |
16. |
Effect of pH on
biodegradation
of polythene
by Serretia
marscence |
Polythene carry
bags |
Weight loss |
Polythene
dumping site |
22.22 % of polythene
degradation per month
was recorded at pH 4,
room temperature with
regular shaking |
Morphological
keys and
biochemical
tests |
Serretia marscence |
[65] |
17. |
Effect of prooxidants
on
biodegradation of
polyethylene
(LDPE) by
indigenous fungal
isolate, Aspergillus
oryzae |
LDPE with
average
molecular
weight of
1,80,000 Daltons
and 8.7 PDI |
Weight loss,
tensile strength
and percentage of
elongation, FTIR
spectroscopy, SEM
analyses |
Previously
reported fungi [59] |
Maximum 47.2% weight
loss, 51% reduction in
tensile strength and 62%
reduction in percentage
of elongation of LDPE
(treated with manganese
stearate followed by UV
irradiation and incubation
with A. oryzae for 3
months). |
Known isolates
was used |
Aspergillus oryzae |
[46] |
18. |
Enviornmental
biodegradation of
polyethylene |
Commercially
environmentally
degradable
polythene |
Epifluorescence
microscopy,
Scanning Electron
Microscopy and
FTIR spectroscopy |
American Type
culture collection
and one was their
own isolate |
After 243 days cross
linking and chain scission
was observed at higher
temperatures leads to
reduction in the molecular
weight |
Known cultures
were used |
Rhodococus
rhodocorous ATCC
29672, Cladosporium
cladosporides ATCC
20251 and Nocardia
steroids GK 911 |
[66] |
19. |
Enzyme-mediated
biodegradation
of heat treated
commercial
polyethylene
by Staphylococcal
species |
Extruded
low-density
polyethylene
(LDPE) with
20-micron
thickness |
SEM and
FT-IR |
Not specified |
Organism BP/
SU1 degrading the
polyethylene layer and
creating holes in it.
Different extracellular
enzymes were
responsible
for the degradation of
shredded polyethylene |
Known cultures
were used |
Staphylococcus epidermis |
[67] |
20. |
High-density
polyethylene
(HDPE)-degrading
potential
bacteria from
marine ecosystem
of Gulf of Mannar,
India |
High-density
polyethylene
(HDPE)
(Commercially
available HDPE) |
Weight loss,
percentage of
crystallinity and
Fourier transform
infrared (FT-IR)
spectrum |
Partially degraded
polyethylene
along with soil
samples
adhering and
adjacent to it was
collected from 15
plastic
waste dumped
sites |
After 30 days of
incubation was nearly
12% (Arthrobacter sp.)
and 15% (Pseudomonas
sp) |
Not specified |
Arthrobacter and
Pseudomonas
sp. |
[68] |
21. |
Impact of soil
composting using
municipal solid
waste on
biodegradation of
plastics |
Polythene carry
bags and cups |
Weight loss and
reduction in tensile
strength |
Two types of
sources: naturally
buried polythene
carry bags and
cups in municipal
composite and
polythene strips
were intentionally
buried in the
composite soil
along with the
solid waste of
municipality
corporation |
In compost culture
highest percentage of
weight loss (11.54%)
was recorded in LDPE1
after 12 months whereas
highest percent loss
in tensile strength was
reported with HDPE1 in
same time of incubation |
Both
morphological
keys and
biochemical
tests were used |
Following were
predominant bacteria
(Bacillus sp.,
Staphylococcus sp.,
Streptococuus sp.,
Diplococcus
sp., Micrococcus sp.,
Pseudomonas sp. and
Moraxella
sp) and fungi
(Aspergillus
niger, A. ornatus, A.
nidulans, A. cremeus, A.
flavus,
A. candidus and A.
glaucus) found to be
associated with degraded
polythene bags and cups
after 12 month |
[69] |
22. |
Investigation on
biodegradability
of polyethylene
by Bacillus cereus
strain Ma-Su
isolated from
compost
soil |
LDPE and
BPE 10 (10
% oxobiodegeradable
additive) |
Change in tensile
strength, percent
elongation, FT-IR
spectroscopy,
Contact angle and
surface energy and
SEM analyses |
Municipal
compost yard |
Pre-treated BPE10 after
3 month of incubation
with the B. cereus (C1)
changes its tensile
strength up to 17.036%
and 17.4o reduction in
Contact angl. |
Morphological
keys,
biochemical
tests and
molecular
markers |
Bacillus cereus (C1) |
[70] |
23. |
Occurrence and
recalcitrance of
polyethylene bag
waste in Nigerian
soils |
Polyethylene
bag wastes
(pure water
sachets) |
Percentage of weight
loss |
Soil samples in a
refuse
dumping site |
After 8 weeks, only
1.19% weight loss was
recorded when treated
with 0.5 M HNO3
followed by slight change
in the colour |
Not specified |
Pseudomonas
aeruginosa, Pseudomonas
putida, Bacillus subtilis and
Aspergillus niger |
[71] |
24. |
Polymer
Biodegradation
of disposable
polyethylene by
fungi
and Streptomyces
species |
Disposable
plastic films |
Average weight loss,
change in tensile
strength and percent
elongation |
Nile River Delta
(Streptomyces),
Northern Regional
Research Laboratory
USDA
(fungi Mucor rouxii
1835) their own
culture collection
(Aspergillus
flavus) |
The average reduction
in the percent elongation
with bacterial and fungal
cultures were recorded
as 28.5% and 46.5%
respectively. This was
preliminary report of
extracellular enzyme(s)
responsible for degrading
of attacking degradable
polythene (ten days heat
treated) |
Morphological
keys |
Eight Streptomyces
strains and two fungi, M.
rouxii NRRL 1835 and
Aspergillus flavus |
[48] |
25. |
Polythene and
plastics-degrading
microbes from the
mangrove soil |
Polythene bags
and plastic cups |
Percentage of weight
loss |
Mangroves
rhizosphere soil |
20.54 ± 0.13
(Psedumonas sp.) 28.80
± 2.40 (Aspergillus
glaucus) percent of
weight loss per month in
shaker culture |
Morphological
keys were used |
Streptococcus,
Staphylococcus,
Micrococcus (Gram
+ve), Moraxella, and
Pseudomonas (Gram –ve)
and two species of fungi
(Aspergillus glaucus and
A. niger) |
[72] |
26. |
Polyethylene
degradation by
lignin-degrading
fungi and
manganese
peroxidase |
High-molecularweight
polyethylene |
Changes in relative
elongation
and relative
tensile strength
(Strograph-R3)
and polyethylene
molecular weight
distribution (Waters
model 150 -C) |
Not specified |
Relative elongation (91.2
± 9.0 %) Relative tensile
strength (100.0 ± 1.3
%) were recorded using
MnP treated with 0.2mM
MnSO4 and 50mM
acetate. MnP is the key
enzyme in polyethylene
degradation by
lignin-degrading fungi |
Not specified |
Phanerochaete
chrysosporium ME-446,
Trametes versicolor
IFO 7043, and IZU-15413 |
[7] |
27. |
Polyethylene
biodegradation
by a developed
Penicillium–
Bacillus
biofilm |
Degradable
polyethylene |
Percent weight loss
and emission of CO2
gas chromatography
(GC) |
Different types of
polythenes were
dumped under
soil were used
for isolation of
microbes
after 2-4 years |
When P. frequentans
and B. mycoides were
used together Weight
loss 7.150 % ( pre-heated
at 70°C) and 6.657%
(unheated) after 60 days |
Morphological
keys and
biochemical
tests |
The most effective
fungi and bacteria were
Penicillium frequentans
and
Bacillus mycoides |
[50] |
28. |
Polythene
degradation
potential of
Aspergillus niger |
Polythene carry
bags |
Weight loss |
Polythene
dumping site |
25% of weight was
observed after 8 months
with regular shaking |
Morphological
keys |
Aspergillus niger |
[73] |
29. |
Production of
an extracellular
polyethylenedegrading
enzyme(s)
by Streptomyces
species |
Starch polyethylene prooxidant
degradable
plastics |
FTIR spectra,
mechanical
properties, and
polyethylene
molecular weight
distributions |
Lignocellulose degrading
microbes but
source was not
specified |
All three bacterial
extracellular enzyme
concentrates leads to
detectable changes in the
degradable plastic as
determined by the FT-IR
spectrometer and tensile
strength (kg/mm2) %
elongation strain energy
(Kg mm) |
Known cultures
were used |
Extracellular enzymes of
the following microbes
such as Streptomyces
badius 252, Streptomyces
setonii 75Vi2, and
Streptomyces viridosporus
T7A |
[35] |
30. |
Screening of
polyethylene
degrading
microorganisms
from garbage soil |
Low density
polyethylene
powder |
Weight loss |
Garbage soil
samples (waste
disposable site
dumped with
polythene bag
and plastic
cup |
Actinomycetes
(Streptomyces KU8)
leads to 46.16% weight
loss of the polythene
whereas bacteria
(Pseudomonas sp) and
fungi (Aspergillus flavus)
degraded only 37.09%
and 20.63 % after six
months |
Morphological
keys and
biochemical
tests |
Streptomyces KU8,
Streptomyces KU5,
Streptomyces KU1,
Streptomyces
KU6,Pseudomonas sp.,
Bacillus sp.,
Staphylococcus sp.,
Aspergillus nidulans and
A. flavus |
[74] |
31. |
Studies on
biodegradation of
polythene |
Polythene carry
bags |
Weight loss, TLC,
GC-MS and FTIR
analyses |
Plastic dumping
sites, ARI, Pune
and NCL Pune |
After eight months
of regular shaking
maximum percentage of
weight loss was recorded
at room temperature with
pH 4 i.e., 50% with fungi
(Phanerochaete
chrysosporium) and
35% with bacteria
(Pseudomonas
aeruginosa) |
Morphological
keys and
Biochemical
tests |
Serratia marcescens
724, Bacillus cereus,
Pseudomonas aeruginosa
, Streptococus aureus
B-324, Micrococcus lylae
B-429, Phanerochaete
chrysosporiu, Pleurotus
ostretus, Aspergillus niger
and Aspergillus glaucus |
[47] |
32. |
Studies on the
biodegradation
of natural
and synthetic
polyethylene by
Pseudomonas
spp |
Natural
polyethylene
(6% vegetable
starch) and
synthetic
polyethylene |
Percentage of weight
loss |
Three sites: 1.
Soil from domestic
waste disposal
site. 2. Soil
from textile
effluents drainage
site and 3. Soil
dumped with
sewage sludge |
The highest weight loss
percentage of natural
polythene (46.2%) and
synthetic polythene
(29.1%) was reported
with Pseudomonas sp.
collected from sewage
sludge dumping site |
Morphological
keys and
biochemical
tests |
Pseudomonas spp. (P1,
P2, and P3) |
[75] |
33. |
Synergistic effect
of chemical and
photo treatment
on the rate of
biodegradation of
high density
polyethylene by
indigenous fungal
isolates |
High density
polyethylene
films of 0.1μm
thickness |
Tensile strength,
percentage of
elongation,
elongation break and
FTIR
analysis |
High density
polyethylene
(HDPE) film
buried in soil 3
months and then
used as a sources
of microbes |
Aspergillus oryzae
leads 72% reduction in
percentage of elongation
and abiotically treated
HDPE film clearly
showed generation of
carbonyl peak at 1718.32
cm as compare to control |
Molecular level
(16S rDNA
sequencing) |
Aspergillus niger,
Aspergillus flavus and
Aspergillus oryzae |
[76] |
34. |
Thermally treated
low density
polyethylene
biodegradation
by Penicillium
pinophilum
and Aspergillus
niger |
Powdered LDPE |
DSC, X-ray
diffraction XRD,
FTIR and SEM |
Not specified |
After 31 months
maximum 5% reduction
in crystallinity (Aspergillus
niger), 11.07% change
in crystalline thickness
(Pencillium pinophilum),
P. pinophilum incubated
with and without ethanol
showed a higher TOLDPE
biodegradation
efficiency than did A.
niger. Mineralization
was also higher for P.
pinophilum with the
addition of ethanol |
Not specified |
Penicillium pinophilum and
Aspergillus niger |
[52] |