Antibacterial Finish for Cotton Fabric from Actinomycetes Isolated from Forest Soil.
Increase concern over the damage caused by exposure to microbes, chemical pesticides, UV light and pollutants in last few years heightened the demand for protective garments. Clothing today is expected to be water proof, flame resistant, self--cleaning, insect repellant and antimicrobial to protect human beings from infection, UV light, chemical and biological agents (7). With the growing public health awareness of the pathogenic effects, malodors and stain formations caused by microorganisms, there is an increasing need for antibacterial materials in many application areas like medical devices, health care, hygienic application, water purification systems, hospital, dental surgery equipment, textiles, food packaging, and storage (8). In order to impart permanent functionality to textile surfaces, biocompatible polymers like chitosan, carrageenan and their derivatives can be used by some chemical strategy using anchoring chemical such as cyanuric chloride and hydroxydichlorotriazine (9). The study also focuses on the application of bioactive molecule extracted from actinomycetes isolated from forest soil in textile finish. An attempt was made to coat 100% cotton fabric with chitosan and sodium alginate and the bioactive biomolecule produced by the potent actinomycetes isolate.
MATERIAL AND METHODS
Collection of soil sample
Three soil samples were collected at the depth of 5-m10 cm in sterile plastic bags from three different forest areas, Tamil Nadu, India. All samples were transported to the laboratory, labeled and refrigerated for further study (10).
Two different pretreatments were done on soil samples. The soil samples were air dried for 3-4 days at room temperature. And wet heating was performed at a temperature of 70[degrees]C for 15 minutes in a water bath (11, 12).
Isolation of actinomycetes
1 g of pretreated soil samples were suspended in 10 ml distilled water and vortexed for 10 minutes and serially diluted to [10.sup.-6]. 0. 1 ml of aliquots was taken from each dilution and spread plating was done on Actinomycetes isolation agar and incubated at room temperature for 7 days (13).
Morphological characters such as colony characteristics, type of aerial hyphae, growth of vegetative hyphae, soluble pigment production were observed (14).
Gram staining was performed and phase contrast microscopy was done after performing agar slide culture
Bacterial strains used
Four bacterial strains were used for this study. They were Escherichia coli(MTCC 443), Bacillus subtilis (MTCC 441), Staphylococcus aureus (MTCC 737)and Klebsiella sp (MTCC 418).
Primary screening of isolate was done to ascertain the potential of strains with respect to the production of antimicrobial secondary metabolites. On the basis of primary screening results, isolates showing substantial antimicrobial activities are selected for subsequent secondary screening programme (15). Primary screening was done by right angle streak method (16). During the primary screening, isolates were screened against selected bacterial strains by using perpendicular streak. In this method nutrient agar medium was used and each plate was streaked with individual isolate at the center / diameter of the plate and incubated at 30[degrees]C for 7 days. Later 24 h old fresh subculture of test organisms were prepared and streaked perpendicular to the isolate and incubated at 37[degrees]C for 24 h. zone of inhibition was observed after incubation.
Preparation of crude extract
The active isolate resulted from primary screening were used for their extracellular antibiotic production capabilities under submerged fermentation conditions. The production medium containing starch 1%, potassium nitrate 0.2%, sodium chloride 0.2%, Di- potassium hydrogen phosphate 0.2%, MgS[O.sub.4] 0.005%, CaC[O.sub.3]0.002%, ferrous sulphate 0.001%, casein 0.03% and sea water 50% was used for antibiotic production. 7 days old slant culture of selected isolates was used for inoculum preparation. Sterile distilled water was added to each slant and 5 ml of this spore suspension was added to 45 ml of the production media and incubated at 28[degrees]C on a rotary shaker (120 rpm) for 4 days. Then samples were collected in to sterile centrifuge tube and centrifuged at 3000 rpm for 15 minutes. The supernatant was filtered through Whatman No.1 filter paper. The filtrate was aseptically transferred in to a sterile conical flask and stored at 4[degrees]C for further assay.
Extraction of the antimicrobial compound from culture supernatant using different solvents and purification by column chromatography
The extraction of active compounds from crude culture broth was done using different solventslike n-butanol, n-hexane, ethyl acetate, petroleum ether, methanol and chloroform. The solvents were mixed in the proportion of 1:1. Aqueous layer and organic layers were separated and tested for the presence of antibiotic using disc diffusion method. The partially purified form of active compounds was subjected to further purification by column (17). The dried extract was eluted with chloroform--methanol solvent system. Stepwise elution was done by decreasing the concentration of chloroform and increasing the concentration of methanol. In each successive elution concentration of chloroform was reduced 10% and that of methanol was increased by 10% until the concentration of methanol reached 100%. All the fractions each of 20ml were collected and further analyzed.
Thin layer chromatography
The active compound obtained after solvent extraction was spotted on pre-coated thin layer chromatography plates. The plates were eluted with chloroform: methanol solvent system (4:1) (18). The spotted TLC plates were kept in iodine chamber for the development of spots which corresponds to the antimicrobial compounds.
Secondary screening was done by disc diffusion method (19). The media used was Muller Hinton Agar. The test organisms were prepared by inoculating few colonies in to sterile nutrient broth and incubated at 37[degrees]C until the visible turbidity matches that of 0.5 McFarland solution which is equivalent to 106-108 CFU/ml. On the medium, test organisms were swabbed by sterile swab and left at room temperature for 3-5 minutes for the surface moisture to be absorbed before applying the discs with crude extract. Sterile discs were loaded with 100[micro]l of the crude extract re for the assay of antagonistic activity and filter paper soaked in sterile distilled water was used as control. The plates were incubated at 37[degrees]C for 24 h and the zone of inhibition (mm) was measured.
The fractions which showed the antimicrobial activity were subjected to spectroscopic analysis. UV-visible spectra were obtained on Hitachi U2900 spectrometer and infrared spectra were recorded (20).
Coating of cotton material with bioactive biomolecule
100% cotton fabric was used for biomolecule coating purpose (21).
Pre- treatment of cotton material--scouring and bleaching
The cotton fabric was scoured using 3.0% sodium hydroxide and 2% sodium carbonate and all other auxiliaries prescribed by standard procedure. It was then bleached with 4% hydrogen peroxide and all other auxiliaries as per the standard procedure (22).
Chitosan and sodium alginate polymer coating
Chitosan solution was prepared by stirring a dispersion of chitosan (8g) in 2.0% (v/v) aqueous acetic acid solution for 1hr at 60[degrees]C and then 2g of sodium alginate polymer was added to the chitosan solution and stirred for 10 min. The fabric was padded twice with solution of same concentration and was dried at 80[degrees]C for 5 min and cured at 140[degrees]C for 3 min.
Immobilization of bioactive biomolecule
Active fractions from column chromatography were used as antibacterial agents for this purpose. The column eluents were dried and dissolved in sterile distilled water. 2.0 [+ or -] 0.1 cm fabric samples were taken from the polymer coated cotton fabric and immersed separately in the solutions and allowed to remain stand till 24h. Then they were dried at room temperature (23).
Antibacterial activity assessment
The antibacterial activity was evaluated against Staphylococcus aureus (MTCC 737) and Escherichia coli (MTCC 443). Bioactive material coated fabric samples were placed at the centre of bacteria seeded agar plate. After 24h the plates were observed for the zone of inhibition (24).
RESULTS AND DISCUSSION
A total of 22 actinomycetes were isolated from three different forest soil samples. Microbes were isolated in mixed culture by spread plate method. Based on colony morphology individual actinomycetes were isolated from the plates. [Fig 1]
Morphological and cultural characteristics
Morphological characters such as colony morphology, colour of aerial mycelium, substrate mycelium and production of soluble pigment were studied and tabulated [Table 1]. Gram staining revealed that all the isolates are gram positive in nature.
Agar slide culture and Phase contrast microscopy
Agar slide culture was performed and after incubation time cover slips were removed and observed under phase contrast microscope after staining with lacto phenol cotton blue. Results are shown in [Fig. 2].
Among the 22 actinomycetes isolated from soil sample, six isolate showed antibacterial activity against at least one of the test bacteria. In perpendicular streak method, the result revealed that the isolates KUAJ1 and KUAJ5 possess broad spectrum activities against tested bacteria as shown in [Table2].
Primary screening by right angle streak method. Pathogens used are Escherichia coli (MTCC 443), Bacillus subtilis fMTCC 441), Staphylococcus aureus(MTCC 737) and Klebsiella sp(MTCC 418).
Extraction of active compound
Different solvents were tested for the extraction of active compound. In case of KUAJ1 and KUAJ5 active compound yield observed in the residue extracted with methanol.
The bioactive compounds from methanolic extract were further purified by column chromatography. Twenty eluents were collected and analyzed for antimicrobial activities. Eleventh fraction showed activity against both gram negative and gram positive bacteria in KUAJ1 extract and fifteenth fraction showed activity against test organisms in KUAJ5.
The partially purified bioactive compounds prepared from two isolates were subjected to secondary screening by disc diffusion method in triplicates. The isolate KUAJ1 showed maximum activity against Klebsiella sp and KUAJ 5 exhibited maximum activity against Bacillus sp. Mean zone of inhibition against pathogens are tabulated.
The partially purified antimicrobial compound obtained after solvent extraction was analyzed using pre- coated silica gel plates. Chromatograms were developed in iodine chamber. Rf values were found to be 0.75 and 0.48 for KUAJ1 and KUAJ5 respectively.
Spectroscopic characterization of crude extract
The UV--visible spectra for methanolic extract showed maximum absorption spectra at 218 and 240 nm respectively for KUAJ1 and KUAJ5. The IR spectrum exhibited 3414/cm (broad) and1020.34 (strong) for KUAJ1 and 3433.29, 3404.29, 339.64 (broad) and 1022.27 (strong) for KUAJ 525.
Coating of bioactive biomolecule on cotton
100% cotton cloth was coated with chitosan and sodium alginate polymer. 2.0 [+ or -] 0.1 cm diameter cloth pieces were cut from the polymer coated cotton fabric and subjected for bioactive molecule coating. Coated material was then subjected for antibacterial assessment. The results are tabulated.
Polymer coated fabric sample produced a zone of inhibition of 3.6cm and 3.8cm against the test pathogen Staphylococcus sp and E.coli respectively. Both CP1 and CP5 shown more activity against E.coli, the gram negative test pathogen.
Forest soil samples from Ooty, Tamil Nadu were subjected for investigation and 22 actinomycetes were isolated. On primary screening six isolates showed activity against one or the other of the test organisms in right angle streak method. Potential isolates from primary screening were subjected for secondary screening by disc diffusion method. Among the screened isolates KUAJ1 and KUAJ5 showed intense activity. The active isolates of primary screening when subjected to secondary screening showed different activity from that of primary screening; some of the active isolates did not show the activity in the secondary screening while some showed little activity. According to Bushell (1997) (26), during the screening of novel secondary metabolite, actinomycetes isolates often show antibiotic activity on agar but not in liquid culture. TLC results of KUAJ 1 extract shows an Rf value of 0.75 which is similar to that of kanamycin and KUAJ5 extract with Rf value 0.48 shows similarity with thienamycin whose Rf values is 0. 49 according to Monisha khanna et al. Maximum UV absorbance peak for KUAJ1 is 218 nm and KUAJ5 is 240 nm which are in the range of 215- 217 nm which indicates a highly polyene nature. From UV- visible spectroscopic analysis it was found that both the strains are able to produce broad spectrum antibacterial agents which absorbs at UV range. FTIR results exhibited O-H , C-H and C[H.sub.2-]S groups in KUAJ1 and N-H, CH3-S groups in KUAJ5 extract. Antibacterial activities of polymer coated cotton impregnated with bioactive molecules were also studied. Chitosan and sodium alginate coated cotton fabric produced zone of inhibition as the polymer itself has got some antimicrobial property according to O.L Shanmugasundaram. Antibacterial activity results resemble that of secondary screening results. Both the samples were able to inhibit E.Coli, one of the test pathogen to the maximum. So the results indicate that the bioactive molecules produced by the actinomycetes isolated from forest soil can be applied on textile for antibacterial finish.
Actinomycetes were isolated from forest soil and their antibacterial efficacies were tested. Selected strains KUAJ1 and KUAJ5 exhibited a broad spectrum activity. Antibacterial biomolecules produced by these strains coated on cotton fabric showed antibiogram. Based on these results it has been shown that the forest soils possess various antibiotic producing actinomycetes and may be considered as one of the potential source of bioactive compounds producing actinomycetes which can be used in textile industry for antibacterial finish.
The authors acknowledge the management of Karpagam University for providing all necessary facilities to carry out the study.
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T.R. Juby and R. Usha *
Department of Microbiology, Karpagam Academy of Higher Education, Coimbatore, India.
(Received: 04 February 2018; accepted: 03 March 2018)
* To whom all correspondence should be addressed.
Caption: Fig. 1. Actinomycete colonies on actinomycetes isolation agar
Caption: Fig. 2. Agar slide culture and phase contrast microscopy
(a) Actinomycetes growth on agar slide culture, (b) Phase contrast image of KUAJ1 and (c) Phase contrast image of KUAJ5
Caption: Fig. 3. Primary screening results KUAJ1 and KUAJ5
Caption: Fig. 4. Inhibitory effect of column eluents
Caption: Fig. 5. Infrared spectrum of the partially purified antimicrobial compound produced by KUAJ1
Caption: Fig. 6. Thin layer chromatography
Caption: Fig. 7. Infrared spectrum of the partially purified antimicrobial compound produced by KUAJ5
Table 1. Morphological characteristics and gram reaction of actinomycetes isolates S. Actinomycete Aerial Reverseside Soluble Gram No. Isolate mycelium pigment pigment staining 1 KUAJ1 White Creamy - + white 2 KUAJ2 Cottony White White - + 3 KUAJ3 Green Whitish - + green 4 KUAJ5 Creamy white Yellow Yellow + 5 KUAJ6 Brownish white Grey - + 6 KUAJ22 Golden yellow Deep brown - + '+' positive reaction ' -' negative reaction Table 2. Antibacterial activity of various isolate against test organisms S. Actinomycetes E. coli Klebsiells B. subtilis S. aureus No Isolate sp 1 KUAJ1 + + + + 2 KUAJ2 + - - - 3 KUAJ3 + - - - 4 KUAJ5 + - + + 5 KUAJ6 + - - + 6 KUAJ22 + - - + '+' shows antibacterial activity '-' No antibacterial activity Table 3. Antibiogram of KUAJ isolates against various pathogens S. Test Mean zone of No. Organism inhibition(mm) KUAJ1 KUAJ5 1 E.coli 20 18 2 Klebsiella sp 21 20 3 Bacillus subtilis 18 22 4 Staphylococcus sp 18 16 Table 4. Evaluation of antibacterial activity of polymer and immobilized bioactive biomolecule loaded cotton sample S. Sample Zone of inhibition(cm) No. Staphylococcus sp E. coli 1. CP 3.6 3.8 2. CP1 4.6 4.8 3. CP5 4.2 4.4
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|Author:||Juby, T.R.; Usha, R.|
|Publication:||Journal of Pure and Applied Microbiology|
|Date:||Mar 1, 2018|
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