Molecular and Functional Characterization of Metabolites from Terrestrial Streptomyces hygroscopicus AVS7 Isolated from Western Ghats, India.
MATERIALS AND METHODS
Isolation and screening of isolates from soil sample
The samples were collected from eleven different terrestrial regions Valparai [Stanmore, Selali, Mamika estate, Waverly estate, Eettiyar estate, and Valparai town (1, 2)], Topslip and Marudhamalai hills [(BU1, BU2, BU3) Bharathiar University campus, Coimbatore], Tamil-Nadu, India. For systematic screening of pigmented Actinomycetes to explore the Western Ghats region SCN medium (8) was used for the isolation and enumeration of actinomycetes. Samples were serially diluted at tenfold and plated on starch casein nitrate agar plates supplemented with nystatin (20mg/L) in triplicates to minimize the fungal growth. The samples were incubated at 30[degrees]C for 7 days for sporulation and pigmentation. Eventually, mixtures of colonies were formed and they were purified onto a new SCN agar plates until discrete colonies were formed and subsequently stored at -80[degrees]C in 20% glycerol. The glycerol stocks of strains were taken out and streaked on SCN agar for identification and characterization studies. The pigment producing strains were screened for their antagonistic activity against pathogens following cross streak method. Pigmented Actinomycetes isolates were streaked along the diameter on SCN agar plates and incubated at 30[degrees]C for six days and after incubation, 12 hrs grown cultures of clinical pathogens (procured from PSG Hospitals, Coimbatore, TN) of Gram positive organisms such as Staphylococcus aureus, Staphylococcus epidermidis, Enterococcusfaecalis, Shigella sp and Gram negative organisms such as Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Salmonella typhi, Proteus vulgaris and Bacillus subtilis. These pathogens are facultative anaerobes and majorly cause Gastro Intestinal Infections, Urinary Tract Infections and nosocomial infections. The above stated pathogens were streaked perpendicular to the central strip of actinomycetes culture. Plates were again incubated at 37[degrees]C for 24 hrs and zone of inhibition was measured.
Determination of morphological and biochemical characteristics
The selected strain AVS7 was characterized morphologically following the directions given by the International Streptomyces Project (ISP) (9, 10, 11). The morphology of aerial hyphae, substrate mycelium and spore chain arrangement were determined by light microscopy and Scanning Electron Microscopy (SEM) by cover slip technique, and examined after seven days of growth at 30[degrees]C. The strain grown on different media (ISP 1 to ISP 7 and SCN) was investigated by following directions given in the Bergey's Manual of Systematic Bacteriology. The carbon sources utilization and melanoid production were characterized for the strain AVS7 based on the method of Shirling and Gottlieb (12). In addition to this, biochemical and physiological characters were determined according to the method of Schofield and Schaal (13) and Tresner (14).
Total genomic DNA was isolated based on the method of Edwards (15) with slight modification to obtain consistent cell lysis and DNA recovery. For isolation of DNA, 72 hours old broth culture was prepared in SCN medium. About 1.5 ml of broth culture was centrifuged at 10,000 rpm for 10 min. Supernatant was discarded and 500 [micro]l of solution I (10mM Tris HCl, 10mM Mg[Cl.sub.2], 10mM K[Cl.sub.2], 2mM EDTA) was added, vortex and centrifuged at 10,000 rpm for 10 minutes. Supernatant was discarded and 500 [micro]l of solution II (Sol I + 0.4mM NaCl) was added to the pellet, vortexed and centrifuged at 10,000 rpm for 10 min. To the pellet 500 [micro]l of solution III (10mM K[Cl.sub.2], 0.4mM NaCl, 10mM of [H.sub.2]KP[O.sub.4] & [Na.sub.2]HP[O.sub.4]) was added, vortexed and 30 [micro]l of lysozyme was also added. Mixture was gently tapped and the tube was incubated at 37[degrees]C for 15 min. 50 [micro]l of solution IV (10% SDS) was added and mixed well by inverting. The mixture was incubated at 55[degrees]C for 15 min. To this 500 [micro]l of solution V (5M NaCl) was added and centrifuged at 10,000 rpm for 5 min. The supernatant was transferred to fresh microfuge tube and then 500 [micro]l of isopropyl alcohol was added and centrifuged at 10,000 rpm for 10 min. The supernatant was discarded and 500 [micro]l of 70% ethanol was added and centrifuged at 10,000 rpm for 10 minutes. Finally the supernatant was discarded and the pellet was dried. The pellet was suspended in 20 [micro]l of TE buffer and stored at 20[degrees]C. The Gel electrophoresis was performed and DNA was obtained. The amplification of 16 s ribosomal RNA was done using thermocycler (PTC 150, USA) with universal primers and Taq polymerase using standard protocols. The amplified fragments were sequenced and the sequence was compared with reference species of bacteria for similarity using NCBI (National Centre for Biotechnological Information) BLAST available at http:/ www. ncbi.nlm.nih.gov/. The sequences were taken for phylogenetic tree construction using PHYLIP package. The 16s rRNA sequence was submitted at GenBank, NCBI, USA.
Production and extraction of pigments
The glycerol stock of AVS7 spores were spread on SCN agar plates and incubated at 30[degrees]C for seven to ten days and allowed for good sporulation. The seed medium (SCN) was prepared by inoculating two loops of spores from SCN plates and cultured in Erlenmeyer flasks for the growth of vegetative inoculums. The flasks were incubated at 30[degrees]C for three days on a rotary shaker (180 rpm). The culture of 5% (v/v) inoculums was transferred into 100mL aliquots of production medium (SCN broth) in 20x250mL Erlenmeyer flasks and incubated at 30[degrees]C for seven days on a reciprocating shaker (180 rpm). The culture was centrifuged at 5000 rpm for ten mins at 20[degrees] C; the cell free culture filtrate and biomass was separated. The pigment from mycelia biomass was extracted using polar and non polar solvents. The total pigment from biomass was extracted, filtered and concentrated. The cell free culture filtrate was separated using equal volume of polar and non polar solvents, filtered and concentrated. The crude extract was subjected to GC- MS to find out the metabolites profile and FT- IR analysis was performed to determine the functional groups in the crude extract. This was carried out to elucidate the aliphatic and aromatic compounds present in the crude metabolite profile.
Biological activity of crude extract
Determination of antimicrobial assay
The antimicrobial assay and Minimum Inhibitory Concentrations (MIC) assay were assessed by well diffusion method (16) using crude biomass extract and culture filtrate against facultative anaerobic pathogens such as S. aureus, S. epidermidis, E. faecalis, E. coli, P. aeruginosa, K. pneumoniae, S. typhi, P. vulgaris, Shigella sp, Vibrio cholerae and B. subtilis. Fifty micrograms of cell free culture filtrate extract and crude biomass extract was added in respective wells on Mueller Hinton Agar (MHA) plates which were previously seeded with the above stated pathogens. The diameter of zone of inhibition was measured after 24h of incubation at 37[degrees]C for bacteria. The crude extract which exhibited highest antimicrobial profile was prepared at different concentrations ranging from 0 to 1000[micro]g/[micro]L. The lowest concentration of the total pigment extract which showed activity was considered to be MIC of the extract.
Quorum quenching property
Inhibition of protease and lipase
Protease activity was determined using skim milk agar (SMA) plate (17). S. aureus was inoculated in Tryptic Soy Broth (TSB) as control and TSB with S. aureus, crude methanolic extract as test. After incubation at 37[degrees]C at 180 rpm the filtrate was centrifuged at 12000 rpm for 10 mins and supernatant was collected and filled in respective wells on SMA plates. The digested substrate forms clear areas or zones surrounding the wells if proteolytic enzymes were produced. If the extract inhibits the activity of proteolytic enzymes there will be absence of zone around the sample added wells. Tribuytrin agar medium (TBA) was used to detect the inhibition of lipase for crude extract. If the microorganisms tested have a lipolytic activity, an opaque halo could be easily observed around the colonies. 40 [micro]L of S. aureus in control and in presence of crude extract were added to the respective wells in TBA plates. The plates were incubated at 37[degrees]C for 48 h and observed for the inhibition of lipolytic activity through the absence of zone of clearance.
The human breast cancer cell line (MCF-7) was obtained from National Centre for Cell Science (NCCS), Pune and grown in Eagles Minimum Essential Medium (EMEM) containing 10% fetal bovine serum (FBS). All cells were maintained at 37[degrees]C, 5% CO2, 95% air and 100% relative humidity. Maintenance cultures were passaged weekly, and the culture medium was changed twice a week. The monolayer cells were detached with trypsin-ethylenediaminetetraacetic acid (EDTA) to make single cell suspensions and viable cells were counted using a hemocytometer and diluted with medium containing 5% FBS to give final density of 1x[10.sup.5] cells/ml. one hundred microlitres per well of cell suspension were seeded into 96-well plates at plating density of 20,000 cells/well and incubated to allow for cell attachment at 37[degrees]C, 5% C[O.sub.2], 95% air and 100% relative humidity. After 24 h the cells were treated with serial concentrations of the test samples. They were initially dissolved in neat dimethylsulfoxide (DMSO) and diluted to twice the desired final maximum test concentration with serum free medium. Additional four, 2 fold serial dilutions were made to provide a total of five sample concentrations. Aliquots of 100 [micro]l of these different sample dilutions were added to the appropriate wells already containing 100 [micro]l of medium, resulted the required final sample concentrations. Following drug addition the plates were incubated for an additional 48 h at 37[degrees]C, 5% C[O.sub.2], 95% air and 100% relative humidity. The medium containing without samples were served as control and triplicate was maintained for all concentrations.
3-[4,5-dimethylthiazol-2-yl]2, 5-diphenyltetrazolium bromide (MTT) is a yellow water soluble tetrazolium salt. A mitochondrial enzyme in living cells, succinate-dehydrogenase, cleaves the tetrazolium ring, converting the MTT to an insoluble purple formazan. Therefore, the amount of formazan produced is directly proportional to the number of viable cells. After 48h of incubation, 15[micro]l of MTT (5mg/ml) in phosphate buffered saline (PBS) was added to each well and incubated at 37[degrees]C for 4h. The medium with MTT was then flicked off and the formed formazan crystals were solubilized in 100[micro]l of DMSO and then measured the absorbance at 570 nm using micro plate reader. The% Growth inhibition was determined using the following formula.% Growth inhibition = 100- Abs (sample)/Abs (control) x100. Nonlinear regression graph was plotted between% Cell inhibition and [Log.sub.10] concentration and IC50 was determined using GraphPad Prism software.
Isolation and screening of Actinomycetes
Totally 161 different Actinomycetes strain were isolated from eleven different soil samples collected at Western Ghats, Coimbatore, TamilNadu, India. Out of that 27 were pigmented Streptomyces sp. The pathogens P.aeruginosa, K. pneumoniae and E. faecalis were highly susceptible to the strain AVS 7 with the zone of inhibition of 15 mm, 14 mm and 12 mm respectively.
Determination of morphological and biochemical characteristics
Morphological observations of spore chains under light microscopy with a magnification of 400x and 1000x, the strain on SCN agar was soft and ovoid in shape with smooth surfaces. The elongated chain of spores was flexible; the same was also supported by the images magnified through Scanning Electron Microscopy (SEM) (Fig. 1). The color of the aerial mycelium was pinkish grey and the strain AVS7 produced diffusible reddish brown pigment.
Observation of well developed irregular branched vegetative mycelium and no fragmentation of substrate were seen. The arthrospores were formed in chains with numerous spores and the aerial mycelium was branched monopodially. The physiological and biochemical characteristics were displayed in table 1 and this determines the genus level of the organism as Streptomyces. The strain hydrolysed starch, casein and was found to be producers of enzyme substances citrate, catalase, urease and nitrate reduction. The isolate AVS7 fermented reducing and non reducing sugars lactose, maltose, rhamnose and dextrose. Considerable production of pigment was observed only in starch casein nitrate medium, ISP 2 and ISP 3. Maximum diffusible pigments were seen in SCN medium while less diffusible pigments were observed with ISP 2. Other media used such as ISP 1, ISP 4, ISP 5, ISP 6 and ISP 7 did not induce the production of any pigment but growth of the organism was good in the media used. The organism Streptomyces sp was found to produce maximum spores in SCN medium with the range of pH from pH 7 to 9 and the strain was tolerable upto 5% NaCl concentrations.
A 1121-bp gene sequence was obtained with an amplification using 16SrRNA gene primers for the strain AVS 7. A BLAST search of the GenBank database with this sequence showed its 99% similarity to that of Streptomyces hygroscopicus. Phylogenetic tree was constructed with sequence of Genus Streptomyces members using PHYLIP package. The sequence was submitted in GenBank and obtained a temporary ID (KP732441).
Production and extraction of pigments
Fermentation process of the strain S. hygroscopicus AVS7 was carried on at 30[degrees]C for 7 days at 180 rpm. The pigment production was observed from 3rd day of incubation and the pigment started to explore throughout the incubation period and after 7th day, the pigment production was normal. Accordingly, the fermented broth was harvested on the 7th day for further extraction and purification. Cell free culture filtrate and biomass was separated using centrifugation process and the pigments were extracted using polar solvent ethyl acetate and methanol respectively. The methanolic biomass crude extract contained more pigments than cell free culture filtrate crude extract.
IR spectrum has proven to be the most effective way to give the information about the functional groups present in the compound. Figure 2 shows the FT-IR report for the purified fraction. In that, the stretching frequencies of the IR spectrum recorded 2923.87 & 2855.34 corresponds to Aliphatic -CH stretching and 750.0 corresponds--(C[H.sub.2]) n- in hydrocarbon. No peaks at 3500-3000 which clearly confirms that there is no -OH, NH and aromatic hydrogen in this compound. No peak at around 1600-1500 which further confirms the absence of aromatic carbons. The Gas chromatography--Mass spectrometry was analysed for the crude metabolites extract. The chromatogram was obtained with 4 major peaks which are given in figure 3. The highest peak was with the retention time 31.12 and [R.sub.f] value was 6 with relative abundance 149. The molecular mass was 193.05. From this we can approximately conclude that the compound is a aliphatic keto compound and a carboxylic acid derivative.
Biological activity of the crude extract
Determination of antimicrobial activity
The crude biomass extract and culture filtrate showed good antimicrobial potentials against Gram positive and Gram negative clinical pathogens. S. aureus was found to be highly susceptible to both methanolic biomass extract and culture filtrate extract with the zone of inhibition of 2.6 cm and 1.8cm respectively. Both the extracts showed inhibition against P. aeruginosa with the inhibition zone of 1.0cm and 1.2 cm respectively. The methanolic biomass extract showed an inhibition zone of 1.6 cm and 2.2 cm against K. pneumoniae and V. cholerae (Table 1). The methanolic biomass extract was having highest antimicrobial profile so it was taken to determine the quorum quenching property. To assess the quorum quenching property it is necessary to find out the MIC of the extract. MIC of the crude methanolic biomass crude extract was assayed. 20[micro]g/[micro]L of the pigment extract was found to be effective against all the clinical pathogens. S. aureus and Vibrio cholerae were sensitive to a minimum dose of 10 microlitres of the crude extract.
Quorum quenching property
Inhibition of protease and lipase
Absence of zone of clearance was observed in the assay for proteolytic and lipolytic activity after the stipulated incubation period. The absence of zone of clearance with respect to the control indicated quenching or inhibition of quorum sensing molecules by the crude extract. This means that the crude extract have the ability to stop the QS system which is an essential role in synchronising gene expression and functional co-ordination among bacterial communities.
The potential strain AVS7 exhibited anti cancerous activity at a significant range (Fig 4) and the 50% inhibitory activity was found at 3.66 [micro]g/ml. The regression was 0.9912 which was a significant one and 72% of cell death occurred at 10 [micro]g/ml (Table 2). This crude metabolite was found to be efficient anti cancer product.
Terrestial actinomycetes are the well explored group in bacteria. Most of the antibiotics discovered from actinomycetes belong to genus Streptomyces. Apart from the available drugs we wanted to isolate a novel compound from the terrestrial Streptomyces sp obtained from the unexplored Western Ghats region. Hence the soil samples were collected from the Western Ghats (Nilgiri cluster) and about 121 actinomycetes strains were isolated. Among these 27 were pigmented strains. Screening of these pigmented strains revealed the potency of the isolate AVS7 and this primary screening unveiled that the SCN media was a good base for the production of antimicrobial compounds. From the results of morphology, biochemical, physiology and molecular characterization we found out the AVS7 is Streptomyces hygroscopicus. The spores were numerous on aerial mycelium and they form a chain arrangement. The strain showed a good growth on SCN agar amended with NaCl and the isolate can be placed in intermediate tolerant group and this investigation was similar to the report of Valan et al (18). Most of the antimicrobial compounds were extracted in methanol and ethyl acetate and this has been reported in many investigations. Similarily, in our study also crude extract from the biomass of S. hygroscopicus AVS7 was extracted in methanol. Many of the antibiotics were extracted from Streptomyces sp and antibiotics like daunamycin and irunamycin were extracted using methanol. This antibiotic has the antimcirobicidal effect on pathogenic bacteria (19), as our crude was also extracted in methanol this may also contains a potential antibiotic. As the extract had the antimicrobial potentiality by inhibiting P. aureginosa, E. faecalis and K. Pnuemoniae and major activity was against Gram positive bacteria. Similar report was identified in aerobic filamentous bacterium from soil showed activity against Gram positive bacteria (20). So by this means SCN broth induced the production of antimicrobial metabolites which are pigmented. The same was observed in the research of Valan et alm that the novel Streptomyces sp from Western Ghats was found to have the highest antibacterial effect in MNG broth. This study revealed the excellence of antimicrobials produced by the Streptomyces sp depends mainly upon the media constituents and physiological effectiveness. The influence of antimicrobial compounds was showing the highest activity when SCN was used as sole media. Same piece of work was reported by Holmalahti et al (21) who showed that the nature of medium composition strongly affected antimicrobial compounds production in different organisms. This antimicrobial compounds as crude metabolites were strongly produced and characterized for the presence of functional groups and GC- MS and FT-IR analysis revealed that the metabolite with the highest peak was a carboxylic acid derivative of aliphatic keto compound with the mass of 193.05. These metabolites have the highest antimicrobial profile and developed resistance against the pathogenic organisms. Most of the pathogenic organism resist available antibiotics and develop resistance against it through biofilm formation. A quest arised to identify the interaction of the pigmented secondary metabolites over quorum sensing molecules. Hence it was analysed through protease and lipase assay. However, the contribution of these proteases to the pathogenicity of Staphylococcus sp was highly speculative until now and deserves further investigation. The role for proteases may involve in protection against antimicrobial peptides such as the neutrophil defensins and the platelet microbicidal proteins. These peptides seem to play important roles in host defense. Because these antimicrobial peptides are subjected to proteolytic inactivation of the extracellular proteases production by the staphylococci that may represent a bacterial defense system (22). Since the arlR-arlS locus modifies extracellular proteolytic activity, it is tempting to speculate that this locus might be involved in the virulence of S. aureus. It is not yet known whether ArlR acts directly on protease gene transcription or through interactions with other genes. Promisingly inhibition of these quorum sensing molecules of Gram positive organisms observed through the assays as observed by the earlier reports (23). These sensing was quenched by the antimicrobial metabolites in crude form. Simialrily, lipase is also an important lipolytic enzyme of S. aureus that contributes significantly to the pathogenesis of staphylococcal infection (24). The fact that organisms from deep infections are generally [Lip.sup.+] suggests that lipase plays an important role in tissue invasion (23, 25). Generally, the Gram positive organisms secrete proteases and lipases which act as cell to cell communicating agents. Absence of these molecules in the assay plates indicated the prevention of cell to cell communication of the pathogen by the crude biomass pigment extract. In this regard, the antimicrobial compounds disconnect the communication between the cells which may results in forming the pathogenecity. The mode of prevention may be either due to the inhibition in the production or by quenching the produced quorum sensing molecule is yet to be determined. Majorily, the quenching of these molecules will lead us to discovery of novel antibiotics against skin diseases as lipase was quenched by this crude compound. The understanding of the mechanism will lead to the judicial usage of the compound in inhibiting the pathogens. This research implied that the crude metabolite has the anti cancerous potentiality and the isolated culture have potency to be exploited as the sources of novel cytotoxic molecules showed highest activity at least concentration. Further research will be focussed on knowing the chemical nature of the purified biomolecule for their antimicrobial and anticancer activities.
In conclusion, the Western Ghats terrestrial soil had majority of Streptomyces sp than any other actinomycetes species. The isolated S. hygroscpoicus AVS 7 produced red pigment which possessed the antimicrobial as well as possesses the quorum quenching property. So we suggest that this red pigment can be taken as antibiotic in medical fields. Further the crude extract has to be purified and studied for characterization of the pigmented compound also to be done to make it a potential drug.
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V. Manon Mani [1,2] * (#), A. Parimala Gnana Soundari  (#), S. Ashokraj  and V. Brindha Priyadarisini 
 Department of Biotechnology, Hindusthan College of Arts and Science, Coimbatore- 641028, TN, India.
 Department of Microbial Biotechnology, Bharathiar University, Coimbatore--641046, TN, India.
 Department of Horticulture, Sunchon National University, Jeonnam- 540950, Republic of Korea.
(Received: 10 September 2017; accepted: 23 Ocotber 2017)
* To whom all correspondence should be addressed.
(#) Contributed equally
Tel.: +91-422-4440555; E-mail: firstname.lastname@example.org
Caption: Fig. 1. SEM image of AVS7 spores
Caption: Fig. 2. FT- IR analysis of AVS7 crude extract
Caption: Fig. 3. GC- MS analysis of AVS7 crude extract
Caption: Fig. 4. Cytotoxicity analysis of crude extract of AVS7
Table 1. Antimicrobial profile S. Pathogens Zone of inhibition(cm) No. Methanolic Culture extract filtrate 1 Staphylococcus aureus 2.6 1.8 2 Klebsiella pneumoniae 1.6 0.9 3 Stapylococcus epidermidis 1.0 0.7 4 Pseudomonas aeruginosa 1.2 1.0 5 Enterococcus faecalis 1.0 -- 6 Bacillus subtilis 0.7 -- 7 E .coli 0.9 -- 8 Proteus vulgaris -- -- 9 Shigella sp -- -- 10 Salmonella typhi -- -- 11 Vibrio cholerae 2.2 1.2 '--' No zone of inhibition; cm centimetre; < 0.5cm no inhibition Table 2. Cytotoxicity of AVS7 metabolites Conc ([micro]g) % Cell Inhibition 0.63 10.01021 1.25 24.31052 2.5 40.34729 5 60.7763 10 72.01226
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|Author:||Soundari, V. Manon Mani A. Parimala Gnana; Ashokraj, S.; Priyadarisini, V. Brindha|
|Publication:||Journal of Pure and Applied Microbiology|
|Date:||Dec 1, 2017|
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