Received 29 July 2016; accepted 14 August 2016; published 17 August 2016
A hot spring or a hydrothermal spring comprises warm or hot groundwater which is heated by geothermal heat, the essential heat from earth’s interior. The hot spring water also contains dissolved solids and several elements such as calcium, lithium, radium, and sulphur. Such geothermal hot spring streams provide a favourable condition for the development of microbial mats, which covers physiologically and phylogenetically different groups of prokaryotes, e.g., chemotrophic sulphur bacteria, cyanobacteria and oxygenic phototrophic bacteria, depending on the temperature, pH, sulphide concentration and some other environmental conditions  . Thermophilic micro-organisms present in the hot spring perform a variety of works. One of such important works is metal reduction  . The microorganisms belonging to the thermophilic microbial community can fulfil both degenerative and productive functions. Such microorganisms probably carry out global reduction of metals and seem to play a major role in the deposition of minerals in the earth’s crust.
The nanoparticles have an important role in modern perspective because of their unique optical, thermal, electrical, chemical, and as well as physical properties that are due to a combination of the large proportion of high-energy surface atoms compared to the bulk solid  . The use of nanoparticles offers great potential in environmental remediation (Li et al., 2004) as well as in biomedical anti-oxidants  . Many successful chemical and physical techniques e.g., ultraviolet irradiation, aerosol technologies, lithography, laser ablation, ultrasonic sonication etc. are being used for the synthesis of nanoparticles in large quantities comparatively in a short period but all those methods are expensive and sometimes include hazardous chemicals   . Increasing attentiveness towards biological processes has led the scientists to develop an eco-friendly approach for synthesis of nanoparticles. The assemblies of nanomaterial using biological systems offer relatively clean, nontoxic and eco- friendly methods for synthesis of nanoparticles. Nowadays, many organisms like living plants, plant extracts, bacteria, fungi and human cells are used to produce nano-composites   . Gold nanoparticles (GNPs) are being used in India and China as medicine for revitalization and drug delivery. Furthermore, GNPs have an important role in detection of heavy metals such as lead, cadmium, mercury and arsenic  .
The hot spring at Metaldanga (Metaldanga, Birbhum, West Bengal, India) is one of the virgin hot springs whose microbial consortium is completely in dark. Several bacterial strains were identified from the hot spring out of which one of the bacterial strains (named MDH1) was isolated and purified through serial dilution technique and characterized for the use in various purposes. The isolated strain from Metaldanga hot spring was found to synthesize spherical gold nanoparticles (GNPs) with average size of 13 ± 3 nm. The present investigation thus explores the microbial diversity of a virgin hot spring for its beneficial applications in industry, particularly in synthesis of gold nanoparticle.
2. Materials and Methods
All fine analytical grade chemicals were purchased from the Sigma Chemical Co., USA; Merck, USA and the Spectrochem Pvt. India Ltd., India. Chloroauric acid (AuHCl4) used as gold source, was purchased from Qualigens fine chemicals, Mumbai, India.
2.2. Isolation and Growth Kinetics of the MDH1 Bacterium
Mixed population of thermophilic micro-organisms was collected from the soil of the Metaldanga hot springs. An enrichment culture was developed by growing the mixed population culture in a specific semi-synthetic growth medium which contained 0.1 M Fe(OH)3, 0.6 g∙L−1 Na2HPO4, 0.33 g∙L−1 KCl, 2.5 g∙L−1 Na2CO3, 0.02% yeast extract and 0.5% peptone. The mixed population was grown in the medium having pH 8.0 and temperature 42˚C under anaerobic conditions   .
After development of enrichment culture, a pure bacterial strain was isolated from the enrichment culture by subsequent serial sub-culturing of the enrichment culture where pH and temperature were maintained same as in enrichment culture. In the serial dilution process, 1 ml mother enrichment culture (8 days old containing 108 cells/ml of cultures) was inoculated in 30 ml sterilized growth medium in a sealed pressure vial (100 ml capacity) and the order of dilution was made up to 109. The anaerobic condition inside the vials was maintained by passing CO2 gas through the medium as described earlier  . The serial dilution process was repeated several times for isolation of pure bacterial strain from the highest order diluted culture.
The isolated pure bacterial strain thus obtained was grown in the semisynthetic growth medium at different pH (range 7.0 to 12.0) to optimize the growth pH of the bacterium. The isolated strain was also grown in the medium (with optimized pH) at three different temperatures (42˚C, 65˚C and 72˚C) for optimization the growth temperature. For growth curve of the purified bacterial strain, optical density (O. D.) at 540 nm of the bacterial growth medium using UV-visible spectrophotometer (UV-3101PC, Shimadzu) was measured at different days of incubation (up to 22 days). The measured ODs were then used to determine the bacterial cells population by comparing with the pre-calibrated bacterial growth curve (cells concentration vs. optical density). The bacterial cell concentrations for optimize pH and temperature were measured after 10 days of incubation. All these experiments were repeated at least three times to optimize the growth condition of the isolated bacterium.
2.3. Morphology Study by FESEM
The isolated bacterial cell morphology was studied by the Field Emission Scanning Electron Microscope (FESEM). The bacterial slide was prepared by fixing the bacterial cells on a clean glass slide with 2.5% (v/v) gluteraldehyde. The bacterial slide was then dehydrated by incubating for 15 min in each at graded (5%, 10%, 25% and 50%) aqueous acetone. Samples were then air dried and transferred onto a FESEM alumina supports and sputtered with gold by a coater of Blazers. Slides were observed under FESEM (INSPECT F50 SEM, FEI Europe BV, and Netherlands) and photomicrographs of the bacterial cells were taken in single (40×) magnification  .
2.4. Phylogenetic Analysis
Purified bacterial cells were collected by centrifugation of the cultures and the chromosomal DNA of the bacterium was isolated by using standard phenol chloroform technique   . The 16 S-rRNA gene fragment was then amplified by using the forward and reverse primers for molecular characterization. The primer selection was on Trial and Error basis. The amplification of the gene was done by using multiple consensus primer sequences at random and all possible combinations.
The primers which amplified the gene were as follows
The amplified DNA fragment was then separated and eluted from a 1% agarose gel and purified using the Qiaquick gel extraction kit (Qiagen). The purified PCR product was then sequenced with the same primers. The partial rRNA gene sequence was determined by the di-deoxy chain-termination method using the Big Dye terminator kit and ABI 310 Genetic Analyzer (Applied Bio systems). The sequence similarity was searched on this using BLAST. Phylogenetic analysis of the isolated strain was done by neighbour-joining method where distances between sequences were determined by Kimura’s two-parameter model   . The confidence limits of the branching were performed by Bootstrap analysis  . The partial sequence of 16S-RNA gene was thus obtained and submitted to the GenBank  . The isolated novel strain was phylogenetically characterized and named as strain MDH1.
2.5. Synthesis and Characterization of GNPs
Well grown (7 days old) bacterial culture of MDH1 strain was taken in a polypropylene tube and the bacterial cell pellet was collected by centrifugation at 8000 g at 4˚C for 15 min. The pellet was washed several times by phosphate buffer (pH 7.0) and kept at room temperature for 30 min. A 5 mg of wet cells was added to 2 ml of 1 mM AuHCl4 solution and incubated for 6 h at 25˚C. After incubation, the reaction mixture was turned into ruby red colour that showed the precipitation of GNPs in the solution. The as prepared GNPs was then centrifuged (10,000 g at room temperature) to collect the GNPs. The UV-visible spectrophotometry (Shimazdu, model UV- 1800, Kyoto, Japan from 300 - 800 nm), X-ray diffraction (XRD: The BRUKER D8 ADVANCE), Transmission electron microscopy (JEOL JEM 2100F) were used to characterize the size, shape, surface area and dispersity of the synthesized nanoparticles. The surface charge of the biosynthesized gold nanoparticles were analysed by DLS of Zeta-sizer (Nano ZS-Malvern).
2.6. Statistical Analysis
The whole experimental setup was repeated thrice and data were presented with mean ± standard deviation (S.D.).
3. Results and Discussion
Several bacterial strains having various morphologies were identified by repeated serial dilution technique from the enrichment culture of Metaldanga hot spring. One of these strain which act as template for synthesizing gold nanoparticles was isolated and purified by serial dilution technique. The isolated MDH1 bacterium strain is maintained by sub-culturing the bacterium in the specific semi-synthetic growth medium. The isolated bacterium is a facultative anaerobic and thermophilic in nature which grow well and multiply in anaerobic condition but survive in presence of oxygen. The maximum growth rate of the bacterium is observed around 7 - 8 days of incubation (Figure 1(a)). The optimum growth pH and temperature of the strain are at pH 8.0 (Figure 1(b)) and 42˚C (Figure 1(c)) respectively under anaerobic environment. The bacterial cell morphology was determined by FESEM which showed that the isolated bacterium was coccoid in shape (Figure 2). The Gram staining of the bacterium MDH1 shows that the bacterium is Gram negative in nature. Genomic DNA was isolated from the bacterial sample in which the ~1.5 Kb DNA fragment was amplified using high-fidelity PCR polymerase (Figure 3). The PCR product was cloned at Not I site in pBS vector. Positive clones were screened by colony PCR. Further clones were screened for difference in pattern by digestion with a 4 base cutter. The clones were sequenced bi-directionally using the forward and reverse primer. The sequence data was aligned and analyzed to identify the bacteria and its closest neighbours. Phylogenetic analysis of the partial 16 S-rRNA gene sequence (1421 nucleotides; GenBank accession number KT600031) clearly shows that the isolated MDH1 bacterial strain is affiliated with the family “Pseudomonadaceae” and closest similarity (99%) with Pseudomonas putida H8234 (Figure 4, Figure 5).
Figure 1. Growth of bacterium MDH1. (a) Growth kinetics of the bacterium while grown in semi-synthetic medium at pH 8.0 and temperature 42˚C under anaerobic condition; (b) Growth of the bacterium after 10 days while grown in semi-syn- thetic medium at different pH and temperature 42˚C under anaerobic condition; (c) Growth of the bacterium after 10 days while grown in semi-synthetic medium at pH 8.0 and different temperatures under anaerobic condition.
Figure 2. Morphology of MDH1 bacterium taken by FESEM.
Figure 3. Genomic DNA of MDH1 by gel electrophoresis. Where, Genomic DNA―Lane 1; 16S rRNA gene―Lane 2; 500bp Ladder―Lane 3.
Figure 4. Partial 16S rRNA gene sequence of MDH1.
Figure 5. Phylogenetic tree of MDH1 bacterium as determined by Neighbor Joining Method. The sequence similarity was searched on (BLAST) and phylogenetic analysis was done by neighbour-joining method where distances between sequences were determined by Kimura’s two-parameter model. The confidence limits of the branching were performed by Bootstrap analysis.
The bio-precipitation of GNPs was easily observed by visual inspection of the reaction mixture which turned from yellowish to ruby-red colour in presence of MDH1 bacterium at 6 h of incubation (Figure 1(a)). The change of colour indicated the synthesis of GNPs within the reaction medium. The characteristics absorption spectrum of the synthesized nanoparticles recorded by spectrophotometer (Figure 6) was a clear evidence of gold nanoparticles where absorption maximum of GNPs was appeared at 523 nm as reported earlier  . Our earlier works have shown that one hot spring bacteria isolated from Bakreshwar, West Bengal are able to increase the compressive strength of concrete material when incorporated    as well as to synthesis silica nanoparticles from silicate substrate. The bacterium BKH1 is found to secrete a protein (Bioremediase; UniProt Knowledgebase under the accession no.: P86277) which possesses biosilicification activity  . The protein can act as a template to synthesis silica nanoparticles  . The newly isolated MDH1 bacterial strain does not show any biosilicification activity rather it possesses gold leaching activity. The morphology of the bio- assisted gold nanoparticles are mostly spherical but a few large particles with different shapes such as triangles and quasi-hexagons also observed from FESEM (Figure 7(a)) and TEM (inset of Figure 7(a)) images. The average particle size of the synthesized gold nanoparticles are about 12 ± 3 nm (n = 100; excluding the large particles). Average charge of the synthesized particles was found to be negative as confirmed by zeta potential measurement (Figure 7(b)). The negative charges of the synthesized gold nanoparticles indicated the higher stability of the particles.
The crystal structure and phase composition of the as-prepared product were analyzed by XRD (Figure 8). Three prominent peaks were observed in the diffraction pattern, corresponding to the (111), (200) and (220) Bragg reflections of face-centered cubic gold. This clearly indicates that the formation of gold nanoparticles by using a bacterial cells as template. This morphology of synthesized gold nanoparticles as obtained from FESEM or TEM analysis is consistent with that of XRD measurements.
FTIR spectrum of synthesized GNPs showed the presence of characteristic bands for several functional groups (Figure 9). The presence of phenolic groups by C-C=C symmetric stretch (1590 cm−1) and C-C=C asymmetric stretch (1470 cm−1) along with aromatic group by C-H band (1590 and 2848 cm−1) are observed in the IR spectrum. Presence of aromatic amines (-C6H5NH2) and aliphatic amines (R-NH2) are confirmed by
Figure 6. (a) Synthesis of gold nanoparticles from AuHCl4 solution using MDH1 bacterial template, where Figure 6(a-i) is the pure AuHCl4 solution (control) and Figure 6(a-ii) is the bacteria amended AuHCl4 solution after 6 h incubation; (b) Characteristics UV-visible spectrum of gold nanoparticles.
Figure 7. Morphological (size and charge) analysis of gold nanoparticles. (a) FESEM image of gold nanoparticles and TEM view (inset) of it; (b) Zeta-potential of the gold nanoparticles.
Figure 8. X-ray diffraction pattern of GNPs. Peaks corresponding to the (111), (200) and (220) are the Bragg reflections of face-centered cubic gold.
Figure 9. FTIR spectrum of GNPs showing the presence of different functional groups.
1118 cm−1 and 1390 cm−1 bands. IR band at 1040 cm−1 supports the presence of carbonyl (>C=O) groups of carboxylic acids. IR band for metallic gold is observed near 500 cm−1. A band is observed near 3500 cm−1 due to O-H stretching of water molecules and a sharp band near 2310 cm−1 is observed due to presence of CO2. Compounds with free carboxylic acid group (-COOH) or amino group (-NH2) were attached to gold surface during GNPs synthesis. Compounds with free hydroxyl and amino group (-OH, -NH2) can donate their electron to Au3+ ions to form Au0 and carboxylic and amino moiety can bind to Au0 to stabilize GNPs.
The bacterium MDH1 secretes few proteins in their growth medium (unpublished data). One of these proteins may be responsible to act as a template for synthesis of gold nanoparticles due to its gold leaching activity. The formation of GNPs via a simple biocompatible bacterial template designates an eco-friendly green cost effective methodology in which spherical and smaller (12 nm) nanoparticle size can be obtained. It is therefore concluded that isolation and characterization of hot spring bacteria from different hot springs with temperature variations might have potential technological applications in various fields.
The authors highly acknowledge Mr. N. Bala, Jadavpur University for his support in manuscript preparation. The technical and laboratory facilities of Biophysics laboratory, Department of Physics, Jadavpur University are gratefully acknowledged. The technical support of Mr. Samirul Islam, Material Science Department of IACS, Calcutta is also gratefully acknowledged.
Conflict of Interest
There is no conflict of interest of any kind related to this work.
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