research article antibacterial activity of ph-dependent ...media recording, optics, catalysis, and...
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Research ArticleAntibacterial Activity of pH-Dependent Biosynthesized SilverNanoparticles against Clinical Pathogen
Kethirabalan Chitra and Gurusamy Annadurai
Environmental Nanotechnology Division, Sri Paramakalyani Centre for Environmental Sciences, ManonmaniamSundaranar University, Alwarkurichi, Tamilnadu 627412, India
Correspondence should be addressed to Gurusamy Annadurai; [email protected]
Received 17 February 2014; Revised 26 April 2014; Accepted 5 May 2014; Published 21 May 2014
Academic Editor: Beom Soo Kim
Copyright Š 2014 K. Chitra and G. Annadurai. This is an open access article distributed under the Creative Commons AttributionLicense, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properlycited.
Simple, nontoxic, environmental friendly method is employed for the production of silver nanoparticles. In this study thesynthesized nanoparticles UV absorption band occurred at 400 nm because of the surface Plasmon resonance of silvernanoparticles. The pH of the medium plays important role in the synthesis of control shaped and sized nanoparticles. The colourintensity of the aqueous solution varied with pH. In this study, at pH 9, the colour of the aqueous solution was dark brown, whereasin pH 5 the colour was yellowish brown; the colour difference in the aqueous solution occurred due to the higher productionof silver nanoparticles. The antibacterial activity of biosynthesized silver nanoparticles was carried out against E. coli. The silvernanoparticles synthesized at pH 9 showed maximum antibacterial activity at 50 đL.
1. Introduction
Nanoscience and nanotechnology is an emerging field, whichinvolves in the synthesis, application of nanoscale materials,and structures usually in the range of 1 to 100 nm [1]. Dueto the optical, electronic, magnetic, and chemical propertiesand their possible applications in subsequent technologydevelopment, nanoparticles synthesis has received consid-erable attention in recent years [2]. Metal nanoparticles arehaving considerable interest in the fast-developing area ofnanotechnology because of its applications [3]. Currentlyvarious types ofmetal inorganic nanoparticles zinc, titanium,magnesium, copper, gold, alginate, and silver have beensynthesized using various techniques [4].
Biological synthesis of nanoparticles is an alternativemethod of chemical and physical methods; various organ-isms are used for nanoparticles synthesis, because of itseffectiveness and flexible biological factors [5, 6]. A majoraim of research in nanotechnology is a synthesis of greenernanomaterials and the development of swift and steadfastexperimental protocols for the synthesis of green nanoma-terials includes a range of size, chemical compositions, high
monodispersity and large scale production which are thekey features of nanotechnology [7]. There is a great needto develop clean, nontoxic chemicals and environmentallybenign solvents and renewable materials mediated synthesismethod; thus a biologicalmediated synthesis of nanoparticleshas received significant consideration in the last decade [8].Both unicellular and multicellular organisms produce inor-ganicmaterials by intracellular or extracellularmethod.Mag-netotactic bacteria, diatoms, and S-layer bacteria are goodexamples of microorganisms producing inorganic materials[9].
Metallic nanoparticles have been used in biosensing,media recording, optics, catalysis, and environmental reme-diation [10]. Traditionally silver has been used in customarymedicine to gastronomic items because of their disinfectingeffect [11]. Because of their unique optoelectronic and physic-ochemical properties, silver nanoparticles have attractedremarkable attention. Due to their distinctive properties suchas good electrical conductivity, chemical stability, and cat-alytic and antibacterial activities, the silver nanoparticles aregainingmore interest andmost widely used [12].The noxiousnature of silver nanoparticles against variousmicroorganisms
Hindawi Publishing CorporationBioMed Research InternationalVolume 2014, Article ID 725165, 6 pageshttp://dx.doi.org/10.1155/2014/725165
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has been well known; because of their antibacterial proper-ties, silver nanoparticles are being used in the formulationof dental resin composites and ion exchange fibers and incoatings for medical devices [13, 14].
In this study, the silver nanoparticles were synthesizedby an extracellular synthesis process using Bacillus breviscell culture and then the effect of pH on the synthesisof silver nanoparticles was examined by changing the pHof the aqueous cell filtrate with 0.1 N sodium hydroxideand hydrochloric acid. The synthesized nanoparticles werecharacterized; the antibacterial activity of silver nanoparticleswas examined against E. coli.
2. Experimental
2.1. Materials. Silver nitrate, Nutrient agar, Nutrient broth,Luria Bertani medium, Sodium chloride, and Hydrochloricacid were obtained from Himedia Pvt. Ltd., India. E. coli waspurchased from Microlab, Arcot, Tamilnadu. The bacteriawere isolated from pond water and identified as Bacillusbrevis using Bergeyâs manual.
2.2. Extracellular Synthesis of Silver Nanoparticles. The freshBacillus brevis culture was inoculated in nutrient broth andthe flask was incubated in orbital shaker at room temper-ature for 24 hrs. After 24 hrs the culture was centrifuged at10,000 rpm for 10minutes, and then the obtained supernatantwas collected in a conical flask. 1mM of silver nitrate wasadded to the culture supernatant to the synthesis of thesilver nanoparticles, and then the flask was incubated atroom temperature in orbital shaker for 48 hrs. The UVabsorption spectrophotometer reading was taken at differenttime intervals to monitor the synthesis of silver nanoparticlesextracellularly.
2.3. Effect of pH on the Extracellular Synthesis of SilverNanoparticles. The influences of pH on the extracellular syn-thesis of silver nanoparticles were carried out by changingthe pH of the bacterial extracellular aqueous media. Thedifferent pH was taken (5 and 9) to examine the effect of pHon the synthesis of silver nanoparticles using Bacillus. ThepH of the extracellular aqueous media was changed using0.1 N Hydrochloric acid and 0.1 N Sodium hydroxide. UV-spectrophotometer was used to take the absorption at 24 hrsof incubation.
2.4. Characterization of Biosynthesized Silver Nanoparticles.The silver nanoparticles were synthesized using the above-mentioned process and then the air dried sample wasused to characterization technique. The UV (Perkin Elmer)absorbance spectra were taken at various time intervals atdifferent wavelength. Powder X-ray diffractometer (BrukerD8 Advance uses CuKđź radiation, at the 40 kev in the rangeof 10â80) was used to analyze the nature of the nanoparticles.Scanning electron microscope was used to identify the mor-phology of the synthesized silver nanoparticles. EDAX wasused to show the element of the nanoparticles.The functionalgroups of biologically synthesized dried nanoparticles were
observed using Fourier Transform Infrared Spectrometer(Thermo Nicolet Model: 6700). The sample mixed with KBrand then pressed into thin pellet. Infrared spectra weremeasured at the wavelength in the range of 400â4000 cmâ1.
2.5. Antibacterial Activity of Silver Nanoparticles. The anti-bacterial activity of biosynthesized silver nanoparticles wascarried out against Escherichia coli. Various concen-trations(10 đL, 20 đL, 30 đL, 40 đL, and 50 đL) of silver nanoparticles(synthesized using different pH (5 and 9) and original pH(7.2)) were used for examining the antibacterial activity ofsilver nanoparticles. The well-diffusion method was used todetermine the antibacterial activity of silver nanoparticles;the well was formed in the medium using needle; then thecolloidal silver nanoparticles were pipette out into the wells,and then the plates were incubated at 37âC for 24 hrs. After24 hrs of incubation, the plates were observed for the zone ofinhibition.
3. Results and Discussion
Several physical and chemical methods have been used forthe synthesis of metallic nanoparticles; however, there is aneed to develop simple and ecofriendly method to synthesisthe metallic nanoparticles [15]. As a result of the growingsuccess and simple process for the nanoparticles formation,the biological organisms in this field are swiftly gainingimportance [16]. Silver nanoparticles have attractive physic-ochemical properties; therefore, silver nanoparticles play aprofound role in the area of biology and medicine [17]. In thepresent study, an ecological cost effectivemethod is employedfor the extracellular synthesis of silver nanoparticles usingBacillus brevis cell filtrate.
The preliminary confirmation for the formation of silvernanoparticles was the visual observation of colour change ofthe aqueous solution of bacterial culture. Before (a) the addi-tion of silver nitrate the culture was in yellow colour and after(b) addition of silver nitrate, the extracellular culture colourwas changed to white precipitate and at 24 hrs (c) of reaction,the colour of the solution was changed to brown (Figure 1inset). Kalimuthu et al. [18] synthesized silver nanocrystalsusing Bacillus licheniformis; they obtained the similar colourchanges during the formation of silver nanoparticles. TheUV absorption spectral studies were carried out to confirmthe formation of silver nanoparticles using Bacillus brevis.Figure 1 shows UV absorption spectrum; the peak is foundat 400 nm and the maximum absorption peak occurredat 24 hrs. Because of the excitation of surface Plasmonresonance, the colour change occurred after the addition ofsilver nitrate in the extracellular aqueousmedium; it indicatesthe formation of silver nanoparticles [12]. Prakash et al. [19]synthesized silver nanoparticles using Bacillus megaterium;they obtained the maximum absorption peak at 435 nm andthey stated the band occurred due to the surface Plasmonresonance of silver nanoparticles. Figure 2 shows the effectof pH on the synthesis of silver nanoparticles. At pH 9,the maximum production of silver nanoparticles occurred.The absorption peak occurred at 420 nm and 460 nm for
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0
0.5
1
380 400 410 420 430 440 460 480 500 540 580 620
Abso
rban
ce (a
.u)
Wavelength (nm)
4hrs6hrs16hrs
24hrs48hrs
a b c
Figure 1: UV-spectrophotometer absorption of silver nanoparticlessynthesized using Bacillus brevis, inset (a) bacterial culture beforethe addition of silver nitrate, (b) after addition of silver nitrate, and(c) after 24 hrs of reaction.
pH 9 and pH 5, respectively. The inset of Figure 2 showsthe colour variation of the medium; it indicated that higheramount of silver nanoparticles formation occurred at pH 9.Nayak et al. [20] stated that the band at 420 nm indicatedthe spherical shape of nanoparticles, whereas at 480 nmthe particles are different shapes. Figure 3 shows the XRDpattern of the silver nanoparticles synthesized using Bacillusbrevis. The XRD pattern indicated strong peaks in the entirespectrum of 2đ values ranging from 20 to 80. The silvernanoparticles synthesized in this experiment were in theform of nanocrystals. In the XRD spectrum, the peaks at 2đvalues of 32.24â, 48.11â, 58.64â, and 77.47â analogous to (111),(200), (220), and (311) planes confirmed the face centeredcubic crystalline structure of nanosilver [21]. There was anunassigned peak in the XRD spectrum, due to the presenceof bioorganic phase that occurred in the surface of the silvernanoparticles [22].
Figures 4(a)â4(d) show the SEM and EDX image ofthe biosynthesized silver nanoparticles. In Figure 4(a) theparticles agglomerated and there was no understandableshape. Figure 4(b) shows the SEM image of silver nanopar-ticles synthesized using pH 5; the synthesized particles werehexagonal in shape and the size of the nanoparticleswas in therange of 60â110 nm. Figure 4(c) shows the SEM image of thesilver nanoparticles synthesized using pH9; the particleswerespherical and the obtained particles are 10â40 nm in size.Figure 4(d) shows the EDX spectrum of silver nanoparticles;the strong peak at 3 keV indicated the presence of elementalsilver nanoparticles. The size of nanoparticles is high atacidic pH, because the nucleation process for the formationof silver nanocrystal at acidic pH is slow; thus the lowamount of large size particles formed. While at high pH, fastnucleation process occurred because of the accessibility ofâOH ions; thus high amount of small size particles formed[23].
00.20.40.60.8
11.21.41.61.8
2
320 360 400 440 480 520 560 600
pH-5 pH-9Abs
orba
nce (
a.u)
Wavelength (nm)
59
420nm
480nm
Figure 2: UV-spectrophotometer absorption of the effect of pH onthe synthesis of silver nanoparticles. Inset shows that the colourvariation at pH 5 and the synthesis of silver nanoparticles is low andat pH 9 the production of silver nanoparticles is high.
(111)
(200)
(220) (331)
0
100
200
300
400
500
600
700
800
900
20 30 40 50 60 70 80
Inte
nsity
coun
ts
2đ
Figure 3: X-ray diffractometer of silver nanoparticles synthesizedusing Bacillus brevis.
The FTIR spectrum of silver nanoparticles was synthe-sized using Bacillus brevis (Figure 5). The band at 3412 cmâ1and 2918 cmâ1 represents the OâH, CâC stretching vibration[24]. The band at 1634 cmâ1 represents the âNH stretchingvibration of the amide group [12]. The bands at 1381 cmâ1and 1058 cmâ1 represent the aromatic and aliphatic amines ofCâN stretching vibrations of protein [25]. The FTIR resultsconfirmed that the protein might be responsible for theformation of silver nanoparticles [26].
The well-diffusion method was used to provide evi-dence for the antibacterial activity of biosynthesized silvernanoparticles against E. coli. Figure 6 shows the antibac-terial effect of silver nanoparticles (synthesized using (a)original pH (7.2) (b) pH-5 and pH-(9)) against E. coli. Theantibacterial activity of silver nanoparticles was indicated
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(a)
(a)
110nm
60nm 80nm
(b)
(b)
10nm 40nm
20nm
(c)
(c)
Ag
CO
keV
(d)
Cou
nts
10009008007006005004003002001000
109876543210
(d)
Figure 4: SEM image of the synthesized silver nanoparticles. (a) Original pH (7.1), (b) pH 5, (c) pH 9, (d) EDAX spectrum of silvernanoparticles.
by the formation of the zone and the zone of inhibitionmeasured as mm/diameter.Themaximum zone of inhibitionoccurred at 50 đL concentration of silver nanoparticles. Thesilver nanoparticles synthesized using pH 9 show higherantibacterial activity (13mm) against E. coli. Silver has beenwell-known disinfectant for long years. The use of silvercompounds is reduced due to some limitations; recentlymetallic silver in the form of silver nanoparticles showswell antibacterial activity against manymicroorganisms [27].Small sized nanoparticles showed more antibacterial activitythan large size particles because small sized particles affecta large surface area of the bacteria [28]. There are somepossible mechanisms for the antibacterial activity of silvernanoparticles; early studies reported that the electrostaticinteraction may be possible reason for the antibacterialactivity of silver nanoparticles [29]. Early studies statedthat the bacterial proteins are inactivated by the interactionbetween silver nanoparticles and thiol groups of bacterialprotein. Nayak et al. [20] reported the similar results whileusing silver nanoparticles synthesized by different pH; theystated that the initial pH of the medium, surface area, andshape plays important role in the antibacterial efficiency ofsilver nanoparticles.
4. Conclusion
The silver nanoparticles were synthesized using Bacillusbrevis by extracellularmethod.The different sized and shaped
4491058.88
1380.231622.07
2894.61
3421.200
20
40
60
80
100
120
400 900 1400 1900 2400 2900 3400 3900
Tran
smitt
ance
(%)
Wavelength (nm)
Figure 5: FTIR Spectrum of biosynthesized silver nanoparticlesusing Bacillus brevis.
nanoparticles formed while changing the pH of the aqueoussolution. The biosynthesized silver nanoparticles were inface centered cubic crystalline structure. The proteins whichare present in the bacteria may be possible reason for thesynthesis of silver nanoparticles. The pH of the aqueoussolution plays important role in the antibacterial activity ofsilver nanoparticles; the smallest nanoparticles synthesizedusing pH 9 showed more antibacterial activity than largeparticles which are synthesized using original pH and pH 5.
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10đL
20đL
50đL
40đL30đL
c
(a)
c
10đL 20đL
50đL
40đL 30đL
(b)
c
10đL
20đL
50đL
40đL
30đL
(c)
Figure 6: Antibacterial activity of silver nanoparticles. (a) Silver nanoparticles synthesized using original pH of the extracellular aqueoussolution, (b) silver nanoparticles synthesized at pH 5, and (c) silver nanoparticles synthesized at pH 9.
Conflict of Interests
The authors declare that there is no conflict of interestsregarding the publication of this paper.
Acknowledgment
The authors gratefully acknowledge the DST-FIST spon-sored programme, Department of Science Technology, NewDelhi, India, for funding the research development (Ref no.S/FST/ESI-101/2010) to carry out this work.
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