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Journal of Applied Physics &

Nanotechnology
Research Article

Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium


(Turner) C. Agardh with their Antimicrobial Activity and Potential for
Seed Germination
This article was published in the following Scient Open Access Journal:
Journal of Applied Physics & Nanotechnology
Received December 30, 2017; Accepted January 10, 2018; Published January 25, 2018
Suparna Roy* and Anantharaman P
Centre of Advanced Study in Marine Biology, Abstract
Faculty of Marine Sciences, Annamalai University, Chemical originated Nanoparticles are recognized for their utility in various fields such
Tamilnadu, India
as pharmaceuticals, medicine and also as bio-fertilizer, but Nanoparticles also had been
reported for its toxic effect on the environment and human, so reasonably Nanoparticles
are under safety concern. So, biosynthesis of silver Nanoparticles is now a leading interest
in research with evaluation of their phyto-friendly nature. The aqueous extract of brown
seaweed (Sargassum ilicifolium) had been used for the synthesis of silver Nanoparticles.
The synthesized silver Nanoparticles were characterized using UV-visible spectroscopy,
Fourier Transform Infrared (FT-IR) Spectroscopy and the morphological structure was
characterized with Scanning Electron Microscopy. The antibacterial activity of green
synthesized silver Nanoparticles was assayed against six human pathogenic bacteria
which showed that biosynthesized silver Nanoparticles had high inhibitory activity against
Escherichia coli (0.83 ± 0.05cm), Pseudomonas aeruginosa (0.53 ± 0.05 cm), Proteus
mirabilis (0.46 ± 0.05cm) and Klebsiella pneumoniae (0.4 ± 0.1cm) in comparison
to antibiotic Chloramphenicol (5mg/ml). The phyto-toxicity of bio- synthesized silver
Nanoparticles was investigated by studying its effect on seed germination of Abelmoschus
esculentus and Raphanus sativus var. longipinnatus. The seed germination test showed
that the biosynthesized silver Nanoparticles had quite good promoting effect on germination
of both seeds. The seed germination was 60 percent in case of Abelmoschus esculentus
and seed treated with water also had 60 percent seed germination but in case of Raphanus
seed, the seed germination was 100 percent in comparison to normal water treated seeds
which was 60 percent. This study clearly confirmed that biosynthesized silver Nanoparticles
had accelerating effect on both seed germination and consequently indicated that
biosynthesized silver Nanoparticles is environmentally safe and can be used as nano-bio-
fertilizer after further long duration treatment with plant growth and crop yield.
Keywords: Seaweed, Silver nanoparticles, Seed germination, Antibacterial activity

Introduction
Nanoparticles are peculiar in their physical and chemical properties in comparison
to bulk compounds. So, Nano scale research gain the attention in the modern field
of material science and research groups. In various fields, the novel applications of
Nanoparticles are gradually improving and became as emerging needs. But chemical
originated silver Nanoparticles had been reported for its toxic nature on the vegetation.
So, to know the toxic level and mechanism, chemical originated silver Nanoparticles had
been investigated for its effect on various seed germination such as Wang, et al. (2015)
[1] reported that chemically originated silver Nanoparticles and Silver Nitrate (AgNO3)
had a significant effect on seed germination of Radish (Raphanus sativus L.). The effect
of chemical Fe and Ag Nanoparticles on seed germination had been evaluated for flax
(Linum usitatissimum L, cv. Electra), ryegrass (Lolium perenne L, cv. Tove), and two-
rowed barley (Hordeum vulgare L, cv. Annabell) in combination of soil compositions
by Sayed El-Temsah et al, and the effect of Ag Nanoparticles also had been reported
to evaluate its effect on seed germination of Vigna radiata [2]. The effect of chemical
originated nano silver on seed germination and seedling growth in fenugreek seeds was
investigated by Hojjat [3].
*Corresponding Author: Suparna Roy, Centre of The majority of previous reports showed that chemical originated Ag Nanoparticles
Advanced Study in Marine Biology, Faculty of Marine
Sciences, Annamalai University, Tamilnadu, India, had a toxic effect on seed germination and vegetation. So, eco-friendly and phyto-
Email: suparna09roy@gmail.com friendly biosynthesized silver Nanoparticles may negotiate and replace the toxic

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 2 of 9

effect of chemical originated silver Nanoparticles. Seaweeds kept at room temperature for 72 hours within mechanical shaker
had been reported as raw material for green synthesis of silver at 120 rpm with continuous shaking. The colour change of the
Nanoparticles such as Caulerpa racemosa [4], Turbinaria conoides solution indicated the biosynthesis of Silver Nanoparticles [16].
[5] and some seaweed was evaluated for their potential for seed
Preparation of Seaweed extract: The aqueous seaweed
germination [6-11] which revealed that seaweed synthesized
extract was prepared according to the extraction of seaweed
silver Nanoparticles was not toxic to seed germination but it was
liquid fertilizer (1:20) after an 90 minutes, of boiling, then
promoting the seed germination in comparison to normal water
seaweed solution was kept at room temperature for complete
treatment as well as seaweed extract and seaweed liquid fertilizer.
cooling and the cold seaweed solution was filtered with Whatman
Silver nanoparticles were also reported to their application in
filter paper. The seaweed extract and seaweed liquid fertilizer
medicine to reduce the infection in burn treatment and prevent
the adherence of dental bacterial colonization [12,13]. The was used to study its effect on seed germination of Abelmoschus
seaweed synthesized silver Nanoparticles had been reported for esculentus and Raphanus sativus var. longipinnatus seed.
their antibacterial activity such Padina tetrastromatica [14], and Characterization of Biosynthesized Silver
Turbinaria conoides [15].
Nanoparticles
Though, some previous research was done on antibacterial
activity of seaweeds mediated silver Nanoparticles but many UV-Vis spectrophotometer
seaweed species are yet not explored in this aspect. Therefore, After 72 hours of biosynthesis, for characterization and
the focus of the present study is on antibacterial activity of confirmation of biosynthesis of silver Nanoparticles, the solution
biosynthesized silver Nanoparticles by Sargassum ilicifolium was scanned from 300-700 nm with UV-Vis Spectrophotometer
aqueous extract. So far we know, there are very few reports on the (UV-2600 SHIMADZU).
effect of biosynthesized silver Nanoparticles on seed germination,
so we evaluated the potential of seaweed synthesized silver Fourier Transform Infrared (FT-IR) spectroscopy
Nanoparticles on seed germination to prove its phyto-friendly
The biosynthesized silver Nanoparticles were centrifuged
nature and future use of bio-Nano-fertilizers.
at 5000 rpm for 30 minutes to precipitate the pellet at the
Materials and Methods bottom. The pellet was collected and air dried to make powder
at room temperature for further use. The biosynthesized silver
Synthesis of silver nanoparticles Nanoparticles powder was mixed with Potassium bromide (KBr)
and made a pellet for use in Perkin Elmer FTIR model 2000 to
Seaweed extracts preparation: The seaweed (Figure 1)
identify the functional groups which were responsible for the
had been collected from Vadakkadu Rameshwaram, southeast
green synthesis of silver Nanoparticles.
coast of India and identified with CMFRI taxonomy key and other
available taxonomic key. After repeatedly washed, the cleaned Scanning Electron Microscopy
fresh seaweed was cut into small pieces and small piece of
seaweed of 20 g was pasted as fine paste with mortar and pestle The dry powder of biosynthesized silver Nanoparticles was
and the seaweed paste was dissolved in 100 ml of distilled water sprayed on gold coated copper grid to make the thin film on grid
and boiled for 15 minutes at 60 ̊Cat water baths. The seaweed and images were taken with JEOL JSM-5610LV Scanning Electron
extract was kept at room temperature for cooling, and the cold Microscope for morphological identification of biosynthesized
seaweed extract was filtered with whatman filter paper and the silver Nanoparticles.
extract was used for synthesis of silver Nanoparticles. Antimicrobial activity
Synthesis of Ag-Nanoparticles: The aqueous 1mM solution Antibacterial activity of biosynthesized silver Nanoparticles
of Silver Nitrate (AgNO3) was prepared with Silver nitrate (AgNO3) using an aqueous extract of Sargassum ilicifolium was assayed
powder. For typical biosynthesis of Silver Nanoparticles, 10 ml of by the agar disc diffusion method against six human pathogenic
the aqueous extract of seaweed was added to the 90 ml aqueous
bacteria such as Klebsiella pneumoniae, Pseudomonas aeruginosa,
solution of Silver Nitrate (AgNO3) in 250 ml conical flask and
Staphylococcus aureus, Escherichia coli, Enterococcus faecalis and
Proteus mirabilis which were collected from the Department of
Medical Microbiology, Raja Muthiah Medical College, Annamalai
University. The bacterial cultures were freshly prepared in
nutrient broth, which was sub-cultured from pure culture. After
24 hours of culture, each bacterial culture was inoculated into
the agar plates and kept for 24 hours. The market available
Chloramphenicol antibiotic was used as positive control. The
500mg powder Chloramphenicol was dissolved in 100 ml
autoclaved distilled water to make a concentration of 5 mg/ml.
The 1 mm Silver Nitrate (AgNo3) solution was used as negative
control. The 20µl of seaweed synthesized silver Nanoparticles
solution, the solution of Silver Nitrate and antibiotic were given
Figure 1. Sargassum ilicifolium (Turner) C. Agardh, Division - Phaeophyta,
to sterile paper discs and the discs were placed on bacterial
Class - Phaeophyceae Family - Sargassaceae (09°19’.700’’N and plates. After 24 hours of incubation, the zones of inhibition were
079°19’.072’’E). measured in triplicates from three different plates.

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 3 of 9

Seed germination test


The seeds of Abelmoschus esculentus and Raphanus sativus
var. longipinnatus were sterilized with 5% Sodium hypochlorite
solution for 15 minutes [17]. The sterile seeds were dipped in
biosynthesized silver Nanoparticles solution, normal water, 1 mm
AgNO3 solution, seaweed extract, and seaweed bio-fertilizer for
overnight. In sterile Petri plates, sterile filter papers were placed
and 5 ml silver Nanoparticles solution, normal water, 1 mm AgNO3
solution seaweed extract and seaweed liquid bio-fertilizer were
added to the filter paper, and then treated seeds were placed on
filter paper within Petri plates. Then, Petri plates were covered and
kept at room temperature. After 12 hours germination halted and
the germination percentage, mean germination time, germination
index, relative root elongation, relative seed germination and
germination rate were estimated. Germination parameters were
calculated using the following equations [11,18-20].
Relative root elongation (E) = (Mean root length with NPs)/ Figure 2. Representing (A) the aqueous solution of seaweed extract and (B)
Biosynthesized Silver Nanoparticles solution.
(Mean root length with control) ×100
Relative seed germination= (Seeds germinated with NPs)/
(Seeds germinated with control) ×100
Germination index (GI) = (Relative seed germination) ×
(Relative root elongation)/100
Germination Percentage (GP %) = (Gf/n) × 100 where Gf is the
total number of germinated seeds at the end of the experiment
and n are the total number of the seed used in the test.
Mean Germination Time (MGT) =ΣNiDi/n where Ni is the
number of germinated seeds until the ith day and Di is number of
days from the start of experiment until the ith counting and n is the
total number of germinated seeds.
Germination Rate (GR) = Σ Ni/ Σ Ti Ni, where Ni is the number
of newly germinated seeds at time Ti.
Figure 3. Representing the UV-visible spectrum of biosynthesized Silver
GR = (a/1) + (b-a/2) + (c-b/3) +.....+ (n-n-1/N) (6) Nanoparticles by aqueous extract of Sargassum ilicifolium.

Statistical Analysis
Table 1. FT-IR peak values of the aqueous extract of Sargassum ilicifolium.
Means and standard deviation was estimated from the triplicates Peaks Bonds Functional Groups
measurement of zone of inhibition for antibacterial activity. 3649.52 N-H Stretch , C-H Stretch Amide, Alkane

Results & Discussions 2910.13 O-H Stretch, Carboxylic Acid O-H Carboxylic
1113.95 C-O Stretch, Ester, Ether
Synthesis of silver nanoparticles 538.99 C-Br, C-I Stretch Alkyl halides
514.07 C-Br, C-I Stretch Alkyl halides
The mixing of seaweed aqueous solution with Silver Nitrate
(1mM) solution produced reddish brown colour in comparison
to control, the Silver Nitrate solution (AgNO3) and the aqueous The only aqueous extract which was used for synthesis
seaweed solution which suggested the formation of Ag-NPs of silver Nanoparticles also analysed for FT-IR to identify the
by reduction of the aqueous Ag+ (Figure 2). Due to the surface functional groups which was present in water extract of the
Plasmon vibrations among the produced Silver Nanoparticles, mentioned seaweed which was listed below table 1 and the
the colour change occurred [21]. spectrum is represented at figure 4. The functional groups
which are responsible for the synthesis of silver Nanoparticles
Characterization of Biosynthesized Silver by a reduction of 1 mm AgNO3 with the aqueous extract of the
Nanoparticles mentioned seaweed was listed below table 2 and the spectrum is
UV-Visible spectrophotometer represented at figure 5.

The biosynthesized Silver Nanoparticles was scanned The SEM image (Figure 6) showed the high density, spherical,
from 200nm to 700nm.The absorbance peak at 440 to 460 nm cubical and hexagonal shaped and well distributed Ag-NPs
indicated the biosynthesized of Silver Nanoparticles (Figure 3). synthesized from seaweed extract.

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 4 of 9

Effect of biosynthesized Silver Nanoparticles, seaweed The relative root elongation (500) and relative seed
extract and seaweed liquid bio-fertilizer on seed ger- germination (150) was the highest at 48 hours, for the seeds
mination of Abelmoschus esculentus treated with biosynthesized silver Nanoparticles but germination
index which was 750, the highest germination index for the
The figures 7a-7d showed the effect of biosynthesized Silver seeds treated with biosynthesized Ag-Nanoparticles at 48 hours
Nanoparticles on seed germination of Abelmoschus esculentus.  of treatment (Figure 7a). The effect of biosynthesized Silver
Nanopaerticles and normal water on the seed germination
Table 2. FT-IR peak values of Sargassum ilicifolium mediated biosynthesized of Abelmoschus esculentus was the same. The maximum
Silver Nanoparticles. germination rate was found at 24 hours for both treatments
Peaks Bonds Functional Groups such as biosynthesized Silver Nanoparticles (SL-AgNPs) treated
481.04 C-I, C-Br Stretch Alkyl halides seeds (0.076) and normal water treated seeds (0.076) and the
1019.12 C-F Stretch, C-O Bend Alkyl halides, Ether germination rate was gradually decreased with increased of time
3448.15 O-H Stretch, H-Bond, N-H Alcohol, Amine, Amide (Figure 7d). The mean germination time was gradually increased
2920.20 O-H Stretch, Carboxylic Acid O-H Carboxylic with increase of time for both seeds which may be due to more
2849.30 C-H Bend, C-H Stretch Aldehydes, Alkyl effect and reaction of biosynthesized Silver Nanoparticles
1632.74 C=C Stretch Alkenyl (Figure 7c). The seed germination percentage of normal water
1382.55 N-O Bend, C-F Stretch Nitro , Alkyl halide treated seeds were comparatively higher than biosynthesized

Figure 4. Representing the FT-IR spectrum of aqueous extract of Sargassum ilicifolium.

Figure 5. FT-IR spectrum of biosynthesized silver Nanoparticles synthesized by Sargassum ilicifolium aqueous extract.

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 5 of 9

Figure 6. Representing the SEM images of biosynthesized silver Nanoparticles synthesised by Sargassum ilicifolium aqueous extract.

a b

c d

Figure 7. (a) Seed germination index, (b) Seed germination percentage, (c) Mean seed germination time, (d) Seed germination rate.

Ag-Nanoparticles treated seeds at 24 and 96 hours; but the seed percent seed germination occurred in the case of seeds treated
germination percentage was equal for both seeds treated with with normal water (Figure 8). This result proved that 1mM AgNO3
water and biosynthesized Ag-Nanoparticles at 48 hours (Figure solution was toxic to seed germination of Abelmoschus esculentus.
7b). The two types of seaweed extracts such as normal seaweed The only one seed of Abelmoschus esculentus was germinated
extract and the seaweed liquid bio-fertilizer had no effect on (Figures 8a and 8b). The anatomical study was done for the
seed germination of Abelmoschus esculentus. The 1 mm solution only one germinated seed which was treated with 1mm AgNO3
of AgNO3 was also used as a negative control to study its effect revealed that the root tip with root cap was chocked and damaged
on seed germination in comparison to normal water, but only 20 due to treatment of 1 mm AgNO3 solution, but in case of normal
percent seed germination occur in case of AgNO3 solution and 60 water treatment, the germinated seeds had the normal root with

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 6 of 9

Figure 8. Seed germination percentage of Abelmoschus esculentus in different treatments.

a b

Figure 8a. showing the ladies finger seed germination with normal water and 1 mM AgNO3 solution, 8b. showing the ladies finger seed treated with
seaweed extract.

c d

e f

Figure 8c and 8d. The root of seedling of normal water treated seed showed plenty of branch root development and the sectional simple microscopic
view of normal root with the well-developed vascular system, tissues and its connection with branch roots, (e) and (f) - The root tip treated with 1 mm
AgNO3 solution and sectional simple microscopic view of root with the distorted damaged vascular system and tissues.

fair root cap and shoot growth was comparatively good. But the Effect of biosynthesized Silver Nanoparticles, seaweed
normal seaweed aqueous extract and seaweed liquid fertilizer extract and seaweed liquid bio-fertilizer on seed ger-
extract had a completely negative effect on seed germination. mination of Raphanus sativus var. longipinnatus
After one week of treatment, no seed germination occurred
in case of the seeds treated with seaweed aqueous extract and The effect of biosynthesized Silver Nanoparticles on
seaweed liquid fertilizer of Sargassum ilicifolium (Figures 8c - 8f). seed germination of Raphanus sativus var. longipinnatus was

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 7 of 9

a b

c d

Figure 9. (a) to (d) Representing the effect of biosynthesized Silver Nanoparticles and the aqueous extract of Sargassum ilicifolium on seed germination of
Raphanus sativus var. longipinnatus.

comparatively better than the effect of the normal water, seaweed as a negative control to study its effect on seed germination.
extract and seaweed liquid fertilizer. The seed germination index After one week of observation, there was no seed germination
was the highest at 24 hours (133.33) for seeds treated with of the seeds which was treated with 1 mm AgNO3 solution that
biosynthesized Silver Nanoparticles (SL-AgNPs) but the relative proved the Silver Nitrate solution (AgNO3) had a toxic effect on
seed germination was the highest at 96 hours (200) (Figure 9a). The seed germination of Raphanus sativus var. longipinnatus but the
mean germination time, for biosynthesized Silver Nanoparticles seeds were germinated with normal water treatment (Figure 9e).
was less than the mean germination time of seed treated with The seaweed extract and seaweed liquid fertilizer was also used
normal water at 24 hours, but the mean germination time was as a positive control to study their effect on seed germination of
gradually increased with increase of duration of treatment at 48 Raphanus sativus var. longipinnatus (Figure 9g). After one week
hours and 96 hours (Figure 9c). It indicated that seeds treated of treatment, no seed germination occurred for the seeds treated
with biosynthesized Silver Nanoparticles germinated faster with seaweed extract and seaweed liquid bio-fertilizer (Figure
than seeds treated with normal water, seaweed extract and 9f). The root length germinated seeds of radish and ladies finger
seaweed liquid bio-fertilizer. The germination percentage for were measured with standard measuring scale for calculation of
biosynthesized Silver Nanoparticles treated seeds was increased seed germination parameters (Figure 10a and b).
with time in comparison to normal water treated seeds,
Antibacterial activity
seaweed extract treated seed and seaweed liquid bio-fertilizer
treated seed (Figure 9b). The seed germination percentage was Seaweed synthesized Silver Nanoparticles had the maximum
comparatively higher for seeds treated with biosynthesized Silver inhibitory activity against Escherichia coli (0.83 ± 0.05 cm),
Nanoparticles to increase of time than normal water treated followed by Pseudomonas aeruginosa (0.53 ± 0.05 cm), and
seeds. The germination percentage reached to the maximum at Proteus mirabilis (0.46 ± 0.05 cm). The zone of inhibition of Ag-
96 hours (100). The germination rate was the highest at 48 hours Nanoparticles for mentioning four pathogens was greater than
for biosynthesized Silver Nanoparticles treated seeds (Figure the inhibitory activity of antibiotic Chloramphenicol (5mg/ml)
9d). The 1mM Silver Nanoparticles (AgNO3) solution was used and AgNO3 (1mM) which had very less antibacterial activity in

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 8 of 9

e f

Figure 9. (e) showed the radish seed germination with normal water and 1 mM AgNO3 solution, (f) showed the seaweed extract treated seeds of radish.

Figure 9. (g) Representing seed germination percentage of Raphanus sativus var. longipinnatus in different treatments.

a b

Figure 10. (a) the seedling of raddish and Figure 10 (b) Seedling of ladies finger after treatment with seaweed synthesized silver Nanoparticles
(SL) from Sargassum ilicifolium.

comparison to these four pathogens. But for two pathogens seaweed liquid fertilizer. The 1 mm AgNO3 solution had been
such as Staphylococcus aureus (0.31 ± 0.02cm) and Enterococcus proved to be toxic to the germination of Abelmoschus esculentus
faecalis (0.35 ± 0.05 cm) the zone of inhibition of antibiotic (5mg/ seeds consequently one seed germinated and it was again dried
ml) was greater than biosynthesized Silver Nanoparticles solution. and damaged after 3 days due to distortion and vascular damage
The zone of inhibition of seaweed mediated Nanoparticles for which was shown in the sectional view of root. In case of seeds
Staphylococcus aureus and Enterococcus faecalis was (0.15 ± 0.00 treated with seaweed extract and seaweed liquid fertilizer, no seed
cm) and (0.2 ± 0.03cm) (Figure 11). germination occurred for Abelmoschus esculentus seeds. The seed
germination of Raphanus sativus var. longipinnatus was excellent
Conclusions with the treatment of biosynthesized Silver Nanoparticles where
It can be concluded from this study, that the biosynthesized a germination percentage was 100 at 96 hours in comparison
Silver Nanoparticles had a significant effect on seed germination to normal water, which indicated that the biosynthesized Silver
of Abelmoschus esculentus. For Abelmoschus esculentus seeds, the Nanoparticles had high promoting effect on seed germination
effect of Silver Nanoparticles on seed germination was as equal as promoting of Raphanus sativus var. longipinnatus seed. The
normal water, but biosynthesized Silver Nanoparticles had a better seaweed extract, seaweed liquid fertilizer and 1 mm Silver
effect on seed germination of Raphanus sativus var. longipinnatus Nitrate solution (AgNO3) was proved completely toxic to seed
than seed germination with treatment of seaweed extract and germination of Raphanus sativus var. longipinnatus. For the

Volume 1 • Issue 1 • 002 www.scientonline.org J Appl Phys Nanotechnol


Citation: Suparna Roy, Anantharaman P (2018). Biosynthesis of Silver Nanoparticles by Sargassum Ilicifolium (Turner) C. Agardh with their
Antimicrobial Activity and Potential for Seed Germination
Page 9 of 9

Figure 11. Showing the zone of inhibition of biosynthesized Silver Nanoparticles synthesized by the Sargassum ilicifolium aqueous extract.

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Copyright: © 2018 Suparna Roy, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits
unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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