Physico-Chemical Characteristics and Antibacterial Activity of Chitosan Extracted from Shell of Crab Paratelphusa hydrodromous

 

Gokilavani S1, Vijayabharathi V2* and Parthasarathy R2

1School of Life Science, Department of Zoology, Bharathiar University, Coimbatore

2Department of Botany, Government Arts College, Coimbatore

*Corresponding Author E-mail: vijaybharathii@gmail.com

 

ABSTRACT:

In this study, chitosan was extracted from fresh water crab Paratelphusa hydrodromous shells. In order to determine physico-chemical characteristics of the extracted chitosan, the yield, water and fat binding capacities were measured. In addition, the antibacterial activity of chitosan against Yersinia ruckeri fish pathogenic bacteria was investigated in this study. The results showed that chitosan solution at 0.5 g/kg markedly inhibited the growth of Yersinia ruckeri fish pathogenic bacteria. The results of the study indicate that crab shells are a rich source of chitosan as 38.23 of the shell’s dry weight is consisted of this material. Extracted chitosan were exhibited a lower molecular weight and higher water and fat binding capacities Overall, the results indicated that chitosan was a potential bactericide against bacterial fish pathogen yersinia ruckeri.

 

KEYWORDS: Chitosan, Paratelphusa hydrodromous, physicochemical characteristics, antibacterial activity, Yersinia ruckeri.

 


 

1. INTRODUCTION:

Chitin (b-1, 4-poly-N-acetyl-D-glucosamine) is the second most common polymer after cellulose in nature, existing in the shells of crustaceans like crab, shrimp and lobster as well as in the exoskeleton of marine zooplankton, the cuticle of insects and the cell walls of fungicide. Chitosan (poly-b-1,4-2-amino-2-deoksi-b-D-glu-kopiranoz)is derived by deacetylation of chitin1-3. Due to its biodegradability, biocompatibility, nontoxic and wound healing properties and haemostatic activity, chitosan has received increased attention as one of the promising renewable polymeric materials for various applications4-5. Chitosan is a natural nontoxic biopolymer derived by deacetylation of chitin, a chief component of the shells of crustacea such as crab, shrimp, and craw fish. In recent years, applications of chitosan to the fields of chemical engineering, medicine, food, nutrition, pharmaceuticals, environmental protection and agriculture have received considerable attention6-7. In aquaculture, chitosan is utilized as an immunostimulants to protect salmonids against bacterial disease (Brook trout (Salvelinus fontinalis) against Aeromonas salmonicida and Yersinia ruckeri 8, Rainbow trout (Oncorhynchus mykiss) against A. salmonicida and Vibrio anguillarum9.

 

The waste amount of the shell not used in the factories presents a big potential. This waste is normally likely to affect human health adversely as it could lead to environmental pollution. For this reason, the utilization of this source would not only be beneficial to the industry, but to the community health as well.

 

The aim of the present study was to perform a characterization of the chitosan extracted from Paratelphusa hydrodromous shells with chemical methods. In the characterization of the chitosan, the yield, moisture and ash contents, degree of deacetylation, water and fat binding capacities were measured. In addition, evaluate the antibacterial activity of chitosan against Yersinia ruckeri fish pathogenic bacteria was investigated in this study.

 

2. MATERIALS AND METHOD:

2.1. Collection of Crab raw materials:

The fresh water crabs (Paratelphusa hydrodromous) were collected from Bhavani River in Erode district were washed and dried under sun for a day. The specimens were washed repeatedly in Fresh water to remove all the dirt and sand. They were then taken to the laboratory the viscera and tissues were removed. The exoskeleton of the crustaceans were thoroughly washed with running tap water to remove sand adhered to it, and placed in  hot air oven at 600C for 24 hours. The exoskeleton were subjected to shade dry for 2 days and then placed in hot air oven at 600C for 24 hours. The samples were weighed separately from the raw carapace samples, which was packed in polythene covers and kept in airtight containers.

 

2.2. Extraction of chitosan:

The shells contain approximately 30-40% protein, 30-50% calcium carbonate, and 20-30% chitin on dry basis10. These portions vary with crustacean species and seasons11-12. Isolation of chitosan from crab shell wastes involves three steps demineralization (DM), deproteinization (DP), and deacetylation (DA).

 

2.2.1 Deproteinization:

The shells were deproteinized with 5% NaOH at the ratio of shell to solution of 1:10 (w/v) at 120-130oC for 3hrs. The deproteinized shells were filtered and washed with tap water until NaOH was washed off completely, then dried overnight in a hot air oven at 55-60oC.

 

2.2.2 Demineralization:

The deproteinized shells were demineralized by continuously agitating with 5% HCl at the ratio of 1:10 (w/v, shell to solution) overnight at room temperature. 

 

2.2.3 Deacetylation:

The shells were filtered and washed with tap water until neutral. Then deacetylation of chitosan was carried out by hydrolyzing with 47% NaOH at the ratio of 1:20 (w/v, chitin to solvent) at 120-130oC for an hour. This product was washed and dried overnight at 55- 60oC12.

 

2.3. Characterization of chitosan:

2.3.1 Yield

The chitosan yield was calculated by comparing the weight measurements of the raw material to the chitosan obtained after treatment.

 

2.3.2 Moisture Content:

Moisture content of the chitosan was determined by the gravimetric method13.  The water mass was determined by drying the sample to constant weight and measuring the sample after and before drying. The water mass (or weight) was the difference between the weights of the wet and oven dry samples. Procedures were as follows: weighed and recorded weight of aluminium dish, placed 1.0g of chitosan sample in duplicates in the metal aluminium dish, recorded weight of dish with sample, then placed the sample with the lid (filter paper to prevent or minimize contamination) in the oven. The temperature adjusted in oven to 60oC, and dried the samples for 24 hrs was taken the sample from the oven and placed it in a desiccator until it cools to room temperature. The sample was weighted.

 

Calculated moisture content as:

 

                              (wet weight, g - dry weight, g) x 100

%  Of moisture        ________________________________

         content    =                  (Wet weight, g)

2.3.3 Water Binding Capacity (WBC):

WBC of chitosan was measured using a modified method of Wang and Kinsella14. WBC was initially carried out by weighing a centrifuge tube containing 0.5 g of sample and adding 10 ml of water, mixing on a vortex mixer for 1 min to disperse the sample. The sample contents were left at ambient temperature for 30 min with intermittent shaking for 5 s every 10 min and centrifuged (at 3,500 rpm (6,000 x g) for 25 min. The supernatant was decanted and the tube was weighed again.

 

WBC was calculated as follows:

WBC (%) = [water bound (g)/ initial sample weight (g)] x 100.

 

2.3.4 Fat Binding Capacity (FBC):

FBC of chitosan was measured using a modified method of Wang and Kinsella14. FBC was initially carried out by weighing a centrifuge tube containing 0.5 g of sample, adding 10 ml of olive oil was added mixed with a vortex mixer for 1 min. The contents were left at ambient temperature for 30 min with shaking for 5 seconds every 10 min and centrifuged for 25 min. After the supernatant was decanted, the tube was weighed again. FBC was calculated as follows:

 

FBC (%) = [fat bound (g)/ initial sample weight (g)] x 100.

 

2.3.5 Fourier Transform Infrared spectroscopy (FTIR):

In order to detect the structural changes incurred in the chitosan samples after chemical treatment with sodium nitrite or acetic anhydride, the FTIR spectra of the chitosan sample were acquired before and after treatment using a Fourier transform infrared spectrophotometer. The lyophilized powders were analyzed using the KBr method. Two mg of chitosan powder was mixed with 198 mg of KBr, and pressed into a pellet under a pressure of 13 tons for 10 min.

 

The FTIR spectra were measured in KBr pellets in the transmission mode in the range 400–4000 cm-1. The DA was calculated ratio of A1655 and A3450 are the absorbance of bands at 1655 and 3450 cm-1 respectively.

 

2.3.6 Solubility:

Chitosan powder (0.1 g in triplicate) were placed into a centrifuge tube (known weight) then dissolved with 10 ml of 1% acetic acid for 30 min using an incubator shaker operating at   240 rpm and 25oC. The solution was then immersed in a boiling water bath for 10 minutes, cooled to room temperature (25oC) and centrifuged at 10,000 rpm for 10 min. The supernatant was discarded. The undissolved particles were washed in distilled water (25ml) then centrifuged at10, 000 rpm. The supernatant was removed and undissolved pellets were dried at 60oC for 24hr. Finally, weighed the particles and determined the percentage solubility. Solubility (%) calculated as:

 

(Initial weight of

tube + chitosan)

-

(Final weight of tube + chitosan)

X 100

(Initial weight of

tube + chitosan)

+

(Initial weight of tube)

 

2.4. Antibacterial assay:

Antibacterial activity was measured following the method of Zheng & Zhu15 with slight modification. Nutrient agar plates were prepared for culture of Yersinia ruckeri bacteria. 100 μl bacterial suspensions were spread on the plates followed by 100 μl of chitosan preparation in 5% acetic acid (pH 5.5 to 6.0). Controls were identical except that 100 μl of acetic acid solution (pH 5.5 to6.0) replaced the chitosan solution. All plates were incubated at 28 ± 1°C for 24 h before the total number of colonies was enumerated. Inhibition rate (η) was calculated using the equation

              η (%) =          N1  -  N2        Χ    100

                                           N1

Where N1 and N2 are the amount of colonies developed on the control and experimental plates, respectively.

 

In vitro antibacterial assay was carried out by disc diffusion technique sterile discs with 4mm diameter were impregnated with known amount test samples of the chitosan and positive control contained a standard antibiotic (Ampcillin) disc. Negative controls not comprised sterile disc only. The impregnated discs along with control (incorporated with solvent alone) were placed at the center of Agar Plates, seeded with test bacterial cultures. After incubation at room temperature (37°C) for 24 hrs for bacterial plates, antimicrobial activity was showed in terms of diameter of Zone of inhibition which was measured in mm using caliper or a scale and recorded.

 

3. RESULTS AND DISCUSSION:

The present study to investigate various physiochemical properties of chitosan extracted from Paratelphusa hydrodromous. The results of yield, moisture, water and fat binding capacities of chitosan extracted from Paratelphusa hydrodromous shells were analysed (Table 1).

 

Table 1: Characteristics of Chitosan (%)

Yield

39.23

Moisture

0.48±0.18

Water binding capacity (WBC)

619±50

Fat Binding Capacity (FBC)

525±20

Solubility

80.8±10.7

 

The yield of chitosan was being about 39.23%. A chitosan yield of 14.6% was reported from the carapax of Penaeus monodon16. The moisture content of the chitosan was found to be 0.48±0.18%. The result shows similarities with the moisture content of chitosan obtained from different sources (Artemia urmiana, snow crab processing) 17-18.

 

According to Rout19 WBC for CS ranges between 581 to 1150% with an average of 702%. In the present study the water binding capacity of chitosan was 619%. Similar result has been reported by Cho et al.20 but No et al.21 reported lower results of 355 - 611%. Rout (2001) also reported that the process of decolouration causes a decrease in WBC of Chitosan than those of unbleached crawfish chitosan. Table-1 shows that the WBC of samples is 619±50%. No et al.22 reported that the physicochemical characteristics of chitin and Chitosan influence their functional properties, which vary with species and preparation procedures. Knorr4 noticed that differences in WBC between chitinous polymers possibly were due to dissimilarities in crystallinity, amount of salt forming groups and the residual protein content of the products. In the present study HPTLC result shows the protein level of chitosan.

 

The fat binding capacity of and fresh water crab shell (Paratelphusa hydrodromous) was measured using olive oil. The fat binding capacity of crab chitosan measured 525±20%. The range of FBC found in the present study (525%) was slightly similar to that reported 19 and slightly higher than that (217 - 403%) explained20. Several studies reported a correlation between physicochemical and functional properties of Chitosan.

 

Various absorption bands within the 4000-400 cm range were recorded in the FTIR spectra of chitosan, prepared from crab shell. Different stretching vibration bands were observed in the range 3444.87-2227.94 cm-1related to (N-H) in (NH) associated to primary amines. The presence of methyl group in NHCOCH3 range at1654.92 to 1627 cm-1. CH2 in CH2OH group was observed in 1427.32cm-1 stretch. Glycosidic (C-O-C) linkage was observed in 1153.48cm-1. The presence of CH2 and CO groups were observed in the 1072.42cm-1and 605cm-1.  Parasakthi23  observed  the  FTIR  peaks  at  534.61, 1024.16,  1321.88, 1380.81 and 1640.40  cm-1 in chitin  from  the  shell of S. aculeata which  resembles  the peaks  of  crab  carapace,  legs  and  the  claw. Whereas  in the chitin sample of N. crepidularia (shell and operculum) the  peaks  at  699,  713,  854,  1083,  1478,  1788,  2853, 2923,  3395  and  699, 712,  854,  908,  1082,  1483,  1788, 2853, 2921 and 3401 cm-1 were coincided with  that of  the  shell  and  operculum  samples  confirming  the  presence of chitin.

 

 In the present study the anti-bacterial activity of Yersinia ruckeri was investigated (Table 2). Results showed that there was an increase in antimicrobial activity with increasing chitosan concentration. The highest concentration (0.75%) of chitosan used inhibited Yersinia ruckeri by 85.61±12.85%. 0.50% concentration of chitosan inhibited Yersinia ruckeri to 72.31±10.59% than 0.25% concentration of chitosan which inhibited 44.20±10.8%.

 

Table 2: Antibacterial activity

Samples

Diameter (mm) of inhibitory zone against Yersinia ruckeri

Control

No inhibition

Chitosan

0.57±0.1**

Ampicillin

(positive control)

0.73±0.3*

* Significant  and ** Highly Significant

 

The antimicrobial activity of chitosan has been studied extensively; it has been shown that chitosan acts by disrupting the barrier properties of the outer membrane of gram negative bacteria24. The minimum inhibitory concentration (MIC) of chitosan ranged from 0.05% to more than 0.1% depending on the examined gram negative bacteria which were Escherichia coli, Pseudomonas fluorescens, Salmonella typhimurium and Vibrio parahaemolyticus25. The present investigation confirms and supports the earlier findings regarding usefulness of chitosan as an antimicrobial agent. This is proved that the natural chitosan and its derivatives were having antibacterial and/or antifungal characteristics6,26-29  resulted  in  their  use  in commercial disinfectants. According to literature30-31, chitosan possesses antimicrobial activity against a number of Gram-negative and Gram-positive bacteria.

 

4. CONCLUSIONS:

This study investigated the physicochemical characteristics of chitosan extracted from the shells of Paratelphusa hydrodromous waste, which is discarded without being used and causes environmental pollution. Constitute a significant amount of waste in nature, the production of chitosan from crab shells, natural antibiotics could be developed and used to preventing from the pathogenic bacteria. And their non toxic antibacterial property also could be used as preservatives in the food industries to avoid food spoilages and food borne diseases.

 

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Received on 06.09.2014          Accepted on 22.09.2014        

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Asian J. Res. Pharm. Sci. 4(3): July-Sept. 2014; Page 125-128