- Open Access
Bat guano as new and attractive chitin and chitosan source
© Kaya et al.; licensee BioMed Central Ltd. 2014
- Received: 23 May 2014
- Accepted: 6 August 2014
- Published: 14 August 2014
Chitin is a biopolymer that forms the exoskeleton of arthropods, and is found in the cell walls of fungi. It has a wide range of uses in fields such as cosmetics, pharmacy, medicine, bioengineering, agriculture, textiles and environmental engineering based upon its nontoxic, ecofriendly, biocompability and biodegradability characteristics. Commercially, chitin is obtained from processing the outer skeleton of Crustacea such as shrimp, crab, prawn and crayfish after they have been consumed as food. The study aims to examine the nature of bat guano and to determine if it is a practical source of chitin, which has not been done previously.
In this study, the chitin content of dry bat guano samples was found to be 28%. The bat guano, which was collected from Karacamal Cave, came from the bat species Rhinolophus hipposideros. The chitosan yield of this chitin was 79%. The chitin produced from the bat guano was determined to be in the alpha form according to Fourier transform infrared spectroscopy (FTIR) results. The crystallinity of the chitin and chitosan samples was calculated as 85.49 and 58.51% respectively by X-ray crystallography (XRD) experiments. According to scanning electron microscope (SEM) micrographs, the chitin and chitosan structures were shaped like nanofibers. The thermogravimetric analysis (TGA) results showed that both chitin and chitosan had two step weight losses, which are characteristic of these materials. The nitrogen content of the chitin and chitosan was 6.47 and 7.3% respectively according to the elemental analysis results.
In this research, it has been observed that bat guano can be considered to be an alternative source of chitin and chitosan to crab, shrimp, crayfish and krill.
- Bat guano
Chitin is a structural aminopolysaccharide that and is found in the cell walls of yeast, fungi, protists and diatoms as well forms the exoskeletons of broad variety of invertebrates including sponges, worms, mollusks and, especially, arthropods species. It has a wide range of uses in fields such as cosmetics, pharmacy, medicine, bioengineering, biological materials science, agriculture, textiles and environmental engineering based upon its nontoxic, ecofriendly, biocompability and biodegradability characteristics -. Commercially, chitin is obtained from processing the outer skeleton of Crustacea such as shrimp, crab, prawn and crayfish after they have been consumed as food ,. Recently, there has been a need for new chitin sources in line with the discovery of new usage areas for chitin and its derivatives in areas such as biotechnology and extreme biomimetics -. Some studies have considered the utilization of fungi, insects and corals as alternative chitin sources -. In recent studies, it has been determined that there are insect shells within bat guano and accordingly there is chitin in the bat guano ,. In the current study, the ability to use bat guano as an alternative chitin source was investigated for the first time by means of determining the chitin characteristics within the excreta belonging to bat species that feed on insects.
According to data from the General Directorate of Mineral Research and Exploration in Turkey, there are approximately 40000 caves in Turkey, but only 1250 of those have been discovered and explored . The aforementioned number of caves is only for Turkey. The number of caves across the world will be much greater. As is well known, caves are living spaces for bats and the excreta of these bats has been accumulating for many years and has therefore reached a high level. For instance, in the study conducted by Sikazwe and Waele  in Chipongwe and Kapongo caves in Zambia, 1218 and 2822 tons, respectively, of bat guano stocks were estimated. If bat guano is a viable source of chitin, the fact that there is a plentiful supply is a significant advantage.
Bats generally feed on terrestrial arthropods, and the external body parts of all these animals are formed from chitin. The guano within caves of insectivore bats can be utilized as a chitin source. Since bat guano is composed of a good many organic substances it is quite rich in carbon and nitrogen, and can be used in agriculture .
The bat guano used during this study belongs to Rhinolophus hipposideros (Bechstein, 1800). R. hipposideros, also known as the Horseshoe bat, is a bat species that is common throughout Turkey and feeds on insects. Its range is within Southeastern Asia, South and Central Europe and East Africa . It feeds especially on mosquitoes, dragonflies (Odanata) and spiders .
The aim of this study is to examine the nature of bat guano and determine if it is a practical source of chitin, which has not been done previously. Chitosan is the product obtained from chitin. The chitin contents of bat’s dry guano and the chitin’s chitosan productivity will be determined. Moreover, the isolated chitin and synthesized chitosan will be characterized by means of FTIR, TGA, XRD, ESEM and elemental analyses, and their purity will be investigated.
Bat guano samples were dried at 60°C in a drying oven for a week in the laboratory. Afterwards, 10 g of the dried sample were weighed on precision scales and refluxed in 4 M HCl solution for 24 hours at 50°C. Afterwards, it was filtered through 1 μm filter paper and distilled water was added until the pH became neutral. Then, the sample was refluxed in 4 M NaOH solution for 24 hours at 140°C. Next, the refluxed sample was washed with distilled water and filtered via 1 μm filter paper (S & H Labware) until the pH became neutral. Later, samples were once again washed with distilled water and passed through a 1 μm filter paper before blending them with chloroform, methanol and pure water for elemination of pigments, lipids and decolourisation in the ratio of 1:2:4 for 4 hours until the pH became neutral. Finally, the rest of the sample was dried within a drying oven at 60°C for 48 hours, and then weighed to determine the chitin contents of the bat guano.
Chitin extraction procedure was done four times to determine % chitin content.
From the dried chitin, 1 g was refluxed within 60% NaOH solution for 4 hours at 150°C. Later, it was washed with distilled water and filtered through 1 μm filter paper until the pH became neutral, and then it was dried at 60°C for 48 hours. The dry sample was weighted and the amount of chitosan produced from the bat guano was determined.
Fourier transform infrared spectroscopy (FTIR)
Fourier transform infrared (FTIR) spectroscopy was used to identify the chitin formation from the bat guano and the chitosan synthesized from the chitin. Moreover, from an examination of the FTIR bands the form of the chitin can be determined (α, β and γ). In this study, 5 mg samples of the chitin and chitosan from the bat guano were analyzed with a Perkin–Elmer FTIR spectrometer at 4000–625 cm−1.
Thermogravimetric analysis (TGA)
During thermogravimetric analysis (TGA) 3 mg samples of the chitin and chitosan obtained from the bat guano were weighed and a warm-up operation was conducted from 25°C to 650°C by increasing the temperature by 10°C every minute. During this operation, the decomposition temperatures of the chitin and chitosan were noted and the thermal stability was deduced. With this analysis, the temperatures at which maximum decomposition of the chitin and chitosan occurred were identified, while the water content, total decomposed mass and ash content were also determined. For these analyses, an EXSTAR S11 7300 machine was used.
X-ray crystallography (XRD)
I110 = the highest intensity at 2θ 20°.
Iam = the amorphous diffraction intensity at 2θ 13°.
Elemental analysis (EA)
Environmental scanning electron microscopy (ESEM)
A Quanta 200 FEG Environmental Scanning Electron Microscope (ESEM) was used to determine the surface morphology of the chitin and chitosan obtained from bat guano. To enable clear pictures of the samples to be taken during the ESEM analysis a gold coating process was carried out with a Gatan Precision Etching Coating System before filming.
Chitin content and chitosan yield of bat guano
The chitin content in the bat’s (R. hipposideros) dry guano was observed to be 28% by weight. The chitosan productivity of this chitin was determined to be 79%. The chitosan yield of dry bat guano was found to be about 22%. In recent studies, 15–25% chitin has been isolated from the dried exoskeleton of Crustacea such as prawn, shrimp, crab and lobster –. It is noted that the chitin contents of the total body structure dry weight of insects including Agabus bipustulatus, Anax imperator, Bombyx mori, Holotrichia parallela, Hydrophilus piceus, Notonecta glauca, Ranatra linearis and silkworm chrysalides ranges from 10% to 20% among the different species ,–. Alternatively, it was presented by Sajomsang and Gonil  that 36% of cicada sloughs were chitin. In this study it was found that the chitin content of bat guano was higher than the insect species investigated previously and the shell structures of Crustacea including prawn, shrimp, crab and lobster. However, bat guano had a slightly lower chitin content than cicada sloughs. Similarly, it was found that krill and Artemia cyst structures have high chitin contents, like the bat guano ,. Nevertheless, bat guano will be a more prominent source compared with krill and Artemia cyst structures thanks to the natural stocks and easy collection.
In this study, the greater proportion of chitin within bat guano in comparison to the shell structures of Crustacea such as crab, prawn and shrimp will provide an economic advantage. Moreover, upon the collection of the organic and inorganic substances from bat guano with HCl and NaOH, uses for the remaining guano can be researched. Another opinion is to begin chitin isolation following the isolation and use of other organic and inorganic substances within the excreta in the order of their importance. Removing these substances will provide an advantage economically by increasing the chitin content of the bat guano’s dry weight.
Mammals are represented by 5146 species, and approximately 20% of these species are bat species. Among the mammalians, bats have 1116 species followed by the rodentia consisting of 2277 species . Turkey has the greatest variety of bats within the European and Mediterranean regions, which has been determined as 37 species . All except for one species feed on insects, and some bat species are specialized to feed on certain insect groups . Since the guano of insectivorous bats is diversified according to the insect species, the chitin rates obtained from guano belonging to various bat species and the physicochemical features of the obtained chitin will be diverse. Furthermore, the insect variety that the bat consumes as food within its ecosystem will also influence the physicochemical features of the chitin. In this study the isolated chitin was collected from guano belonging to just one bat species. In following studies the chitin contents in the guano of the same or disparate bat species from different environments will be presented along with discrepancies that can be used as a means of characterization of these chitins. Within this study, the utilization of bat guano as a chitin source was conducted for the first time and significant results were observed.
High concentration of HCl and NaOH and long reflux period were required to obtain high quality chitin. Lower concentrations and shorter time were tested but some minerals and protein residues could not be removed efficiently. And also, we found that these are optimum conditions for chitin isolation from the bat guano.
FTIR bands of chitin samples isolated from bat guano and commercial chitin
Functional group and vibration modes
Wavenumber (cm−1) frequency
CH3 sym. stretch and CH2 asym. stretch
CH3 sym. stretch
C = O secondary amide stretch
C = O secondary amide stretch
N–H bend, C–N stretch
CH2 ending and CH3 deformation
CH bend, CH3 sym. deformation
Amida III, components of protein
Asymmetric bridge oxygen stretching
Asymmetric in-phase ring stretching mode
C–O–C asym. stretch in phase ring
C–O asym. stretch in phase ring
CH ring stretching
FTIR bands of chitosan samples obtained from bat guano and commercial chitosan
Wave number (cm −1 ) frequency
Chitosan from bat guano
ν(NH2) assoc. in primary amines and ν (OH) assoc. in pyranose ring
νas(CH2) in CH2OH group
ν (C-H) in pyranose ring
ν (C = O) in NHCOCH3 group (Amide I band)
ν (NH2) in NHCOCH3 group (Amide II band)
δ(CH2) in CH2OH group
δs(CH3) in NHCOCH3 group
δ (C-H) in pyranose ring
Complex vibrations of NHCO group (Amide III band)
ν s(C-O-C) (glycosidic linkage)
νas(C-O-C) (glycosidic linkage)
ν (C-O) in secondary OH group
ν (C-O) in primary OH group
Pyranose ring skeletal vibrations
In addition, the FTIR spectrum results for the chitin and chitosan from bat guano and the FTIR spectrum results for commercial chitin and chitosan purchased from Sigma Aldrich were compared and it was observed that the results showed considerable similarity.
When the results of TGA analyses of chitin and chitosan are considered from previous studies, the mass loss was observed at two stages, which is the same as in the current study ,,,. Nevertheless, when we consider the results in the former studies, it was found that the thermal stability of chitin is higher than chitosan . In this study, it was also observed that the thermal stability of the chitin isolated from the bat guano is higher than that of chitosan. The DTGmax values of the alpha chitin isolated from other organisms such as crab, shrimp or insects are around 380°C, and for chitosan it is 300°C -. The DTGmax values observed for chitin and chitosan in this study also show similarity with former studies. These results show us that the chitin and chitosan isolated from bat guano are in accordance with the results observed in previous studies.
The CrI value of the bat guano chitin was calculated as 85.49%. While the CrI values of chitins isolated from organisms such as crab and insects in former studies were observed to be between 54 and 91% ,. Moreover, it was observed that chitins isolated from fungi and resting eggs have quite low CrI values . The CrI value of chitin isolated from bat guano in this study shows similarity to the chitins isolated from insects and crabs in former studies. In this result, it was observed that the bat guano in this study belongs to R. hipposideros and this species feeds on insects. In addition, it was observed that the external skeleton of the insects could not be digested and was therefore excreted.
The CrI value of the chitosan from the bat guano was calculated as 58.51%. This value is quite low when compared with the Crl value of the chitin. This is due to the stability of the chitin being decreased as a result of deacetylation, and accordingly its crystallinity value is scaled down. The lower Crl value of the chitosan in comparison to the chitin is an indicator that the chitosan is formed form the bat guano chitin. In the study conducted by Abdou et al.  it was noted that the Crl values of the chitosans obtained from cuttlefish, squid pens, shrimp and crab shells ranged between 36 and 71%. The Crl value of the chitosan from the bat guano is moderate in comparison to the values obtained from other living creatures.
It was observed that the chitin isolated from the bat guano contained C, N and H at the rates of 47.52, 6.47 and 6.53% respectively. The N value of completely acetylated chitin was determined to be 6.89% , and the value in this study was close to this rate. The N content of chitin in other studies was observed between 2.96 and 6.8% ,,,. As this value is close to 6.89%, it demonstrates the chitin’s purity. The DA value of the chitin was calculated and set as 128%. The DA value of completely acetylated chitin is 100% . In this study the value observed is greater than 100%, which demonstrates that remnants of inorganic materials have not been completely removed from the chitin. It has been observed that the DA values of chitins isolated from various organisms in previous studies were much greater than 100%. As in these previous studies, it demonstrates that there are remnants of inorganic materials within the chitin structure.
The C, N and H values of chitosan from the bat guano account for 45.2, 7.30 and 7.02% respectively. The higher N value for the chitosan in comparison to the N value of the chitin demonstrates that the chitin is deacetylated and there is chitosan formation. According to the elemental analysis results, the DD value of the chitosan was calculated as 61%. A DD value that is close to 100% demonstrates that the purity of the chitosan is high. It can be stated that the DD value of the chitosan obtained in this study is at a medium to low rate. In follow up studies, the incubation period in the NaOH solution could be prolonged during the process of chitosan synthesis from chitin, so chitosan with a higher DD value can be obtained.
In previous studies, it was observed that the surface of the chitin was formed from three different types in general. The first of these types has the outside surface formed form nanofibers and nanopores ,,. The second has the surface with only nanofibers, without nanopores ,,. The third one has the surface with both nanofibers and nanopores together ,. In this study, the chitin and chitosan obtained from the bat guano have surface morphologies that are formed from only nanofibers, and are accordingly the second type. In the study conducted by Kaya et al. , all the chitins and chitosans obtained from five insect species were formed from only nanofibers. In this study, it is as expected that the surfaces of the chitin and chitosan are formed from only nanofibers as the chitin in the bat guano comes from insect shells.
Chitin and chitosan are biomaterials that can be produced from bat guano and are more economically valuable than the guano that they come from. Bat guano consists of high levels of chitin and chitosan. To utilize this chitin and chitosan effectively, they were characterized with FTIR, TGA, XRD, SEM and elemental analysis methods. Another significant feature of this study was the fact that it was determined that the bats could not digest the chitin and they removed it via excretion. When we take into account the fact that there are probably 100 million tons of bat guano available across the world, it could be a significant source of chitin and its derivatives.
We would like to thank Prof. Dr. Ahmet KARATAŞ for bat species identification. This study was funded by Aksaray University BAP (2014-005).
- Brunner E, Richthammer P, Ehrlich H, Paasch S, Simon P, Ueberlein S, Van Pee KH: Chitin-based organic networks – an integral part of cell wall biosilica from the diatom Thalassiosira pseudonana. Angew Chem Int Ed. 2009, 48: 9724-9727. 10.1002/anie.200905028.View ArticleGoogle Scholar
- Rinaudo M: Chitin and chitosan: properties and applications. Prog Polym Sci. 2006, 3: 603-632. 10.1016/j.progpolymsci.2006.06.001.View ArticleGoogle Scholar
- Bo M, Bavestrello G, Kurek D, Paasch S, Brunner E, Born R, Galli R, Stelling AL, Sivkov VN, Petrova OV, Vyalikh D, Kummer K, Molodtsov SL, Nowak D, Nowak J, Ehrlich H: Isolation and identification of chitin in black coral Paranthipates larix (Anthozoa: Cnidaria). Int J Biol Macromol. 2012, 51: 129-137. 10.1016/j.ijbiomac.2012.04.016.PubMedView ArticleGoogle Scholar
- Aranaz I, Mengibar M, Harris R, Panos I, Miralles B, Acosta N, Galed G, Heras A: Functional characterization of chitin and chitosan. Curr Chem Biol. 2009, 3: 203-230.Google Scholar
- Zhao Y, Park RD, Muzzarelli RA: Chitin deacetylases: properties and applications. Mar Drugs. 2010, 8: 24-46. 10.3390/md8010024.PubMedPubMed CentralView ArticleGoogle Scholar
- Synowiecki J, Al-Khateeb NA: Production, properties, and some new applications of chitin and its derivatives. Crit Rev Food Sci Nutr. 2003, 43: 145-171. 10.1080/10408690390826473.PubMedView ArticleGoogle Scholar
- Dutta PK, Dutta J, Tripathi VS: Chitin and chitosan: chemistry, properties and applications. J Sci Ind Res. 2004, 63: 20-31.Google Scholar
- Ehrlich H: Chitin and collagen as universal and alternative templates in biomineralization. Int Geol Rev. 2010, 52: 661-699. 10.1080/00206811003679521.View ArticleGoogle Scholar
- Park BK, Kim MM: Applications of chitin and its derivatives in biological medicine. Int J Mol Sci. 2010, 11: 5152-5164. 10.3390/ijms11125152.PubMedPubMed CentralView ArticleGoogle Scholar
- Ehrlich H, Simon P, Motylenko M, Wysokowski M, Bazhenov VV, Galli R, Stelling AL, Stawski D, Ilan M, Stöcker H, Abendroth B, Born R, Jesionowski T, Kurzydlowski KJ, Meyer DC: Extreme biomimetics: formation of zirconium dioxide nanophase using chitinous scaffolds under hydrothermal conditions. J Mater Chem. 2013, 1: 5092-5099. 10.1039/c3tb20676a.View ArticleGoogle Scholar
- Wysokowski M, Motylenko M, Bazhenov VV, Stawski D, Petrenko I, Ehrlich A, Behm T, Kljajic Z, Stelling AL, Jesionowski T, Ehrlich H: Poriferan chitin as a template for hydrothermal zirconia deposition. Front Mater Sci. 2013, 7 (3): 248-260. 10.1007/s11706-013-0212-x.View ArticleGoogle Scholar
- Ifuku S, Nomura R, Morimoto M, Saimoto H: Preparation of chitin nano fibers from mushrooms. Materials. 2011, 4: 1417-1425. 10.3390/ma4081417.View ArticleGoogle Scholar
- Liu S, Sun J, Yu L, Zhang C, Bi J, Zhu F, Qu M, Jiang C, Yang Q: Extraction and characterization of chitin from the beetle Holotrichia parallela motschulsky. Molecules. 2012, 17: 4604-4611. 10.3390/molecules17044604.PubMedView ArticleGoogle Scholar
- Ferreira RL, Prous X, Martins RP: Structure of bat guano communities in a dry Brazilian cave. Trop Zool. 2007, 20: 55-74.Google Scholar
- Wurster CM, McFarlane DA, Bird MI, Ascough P, Athfield NB: Stable isotopes of subfossil bat guano as a long-term environmental archive: insights from a grand canyon cave deposit. J Cave Karst Stud. 2010, 72: 111-121. 10.4311/jcks2009es0109.View ArticleGoogle Scholar
- Topçu A, Seyyar O, Demircan N: A contribution to the cave spider fauna of Turkey (Araneae). Zool Middle East. 2013, 59: 91-92. 10.1080/09397140.2013.795075.View ArticleGoogle Scholar
- Sikazwe ON, De Waele B: Assessment of the quality and reserves of bat guano at chipongwe and kapongo caves near lusaka as fertiliser material. Unza J Sci Technol. 2004, 1 (3): 32-42.Google Scholar
- Bird MI, Boobyer EM, Bryant C, Lewis HA, Paz V, Stephens WE: A long record of environmental change from bat guano deposits in Makangit Cave, Palawan, Philippines. T Roy Soc Edın-Earth. 2007, 98: 59-69.Google Scholar
- Jacobs D, Cotterill FPD, Taylor PJ, Aulagnier S, Juste J, Spitzenberger F, Hutson AM: Rhinolophus hipposideros. IUCN 2013. IUCN Red List of Threatened Species. 2008, Version 2013.2. <www.iucnredlist.org> Downloaded on 13 February 2014, [www.iucnredlist.org]Google Scholar
- Csorba G, Ujhelyi P, Thomas N: Horseshoe bats of the world (Chiroptera: Rhinolophidae). 2003, Alana Books, Shropshire, United KingdomGoogle Scholar
- Abdou ES, Nagy KSA, Elsabee MZ: Extraction and characterization of chitin and chitosan from local sources. Bioresource Technol. 2008, 99: 1359-1367. 10.1016/j.biortech.2007.01.051.View ArticleGoogle Scholar
- Al Sagheer FA, Al Sughayer MA, Muslim S, Elsabee MZ: Extraction and characterization of chitin and chitosan from marine sources in Arabian Gulf Carbohydr. Polym. 2009, 77: 410-419.Google Scholar
- Youn DK, No HK, Prinyawiwatkul W: Physicochemical and functional properties of chitosans prepared from shells of crabs harvested in three different years. Carbohydr Polym. 2009, 78: 41-45. 10.1016/j.carbpol.2009.03.038.View ArticleGoogle Scholar
- Zhang M, Haga A, Sekigushi H, Hirano S: Structure of insect chitin isolated from beetle larva cuticle and silkworm (Bombyx mori) pupa exuvia. Int J Biol Macromol. 2000, 27: 99-105. 10.1016/S0141-8130(99)00123-3.PubMedView ArticleGoogle Scholar
- Paulino AT, Siminato JI, Carcia JC, Nozaki J: Characterization of chitosan and chitin produced from silkworm chrysalides. Carbohydr Polym. 2006, 64: 98-103. 10.1016/j.carbpol.2005.10.032.View ArticleGoogle Scholar
- Kaya M, Baran T, Mentes A, Sezen G, Asaroglu M, Tozak KO: Extraction and characterization of α-chitin and chitosan from six different aquatic invertebrates. Food Biophys. 2014, 9: 145-157. 10.1007/s11483-013-9327-y.View ArticleGoogle Scholar
- Sajomsang W, Gonil P: Preparation and characterization of α-chitin from cicada sloughs. Mater Sci Eng. 2010, 30: 357-363. 10.1016/j.msec.2009.11.014.View ArticleGoogle Scholar
- Tajik H, Moradi M, Rohani SMR, Erfani AM, Jalali FSS: Preparation of chitosan from Brine shrimp (Artemia urmiana) cyst shells and effects of different chemical processing sequences on the physicochemical and functional properties of the product. Molecules. 2008, 13: 1263-1274. 10.3390/molecules13061263.PubMedView ArticleGoogle Scholar
- Wang Y, Chang Y, Yu L, Zhang C, Xu X, Xue Y, Li Z, Xue C: Crystalline structure and thermal property characterization of chitin from Antarctic krill (Euphausia superba). Carbohydr Polym. 2013, 92: 90-97. 10.1016/j.carbpol.2012.09.084.PubMedView ArticleGoogle Scholar
- Wilson DE, Reeder DAM: Mammal Species of the World. A taxonomic and geographic reference. 2005, Johns Hopkins University Press, BaltimoreGoogle Scholar
- Karataş A, Sachanowicz K: Noteworthy bat records from Upper Mesopotamia, Turkey (Chiroptera). Lynx (Praha). 2008, 39: 103-108.Google Scholar
- Whitaker JO, Karatas A: Food and feeding habits of some bats from Turkey. Acta Chıropterol. 2009, 11: 393-403. 10.3161/150811009X485611.View ArticleGoogle Scholar
- Focher B, Naggi A, Torri G, Cosani A, Terbojevich M: Chitosans from Euphausia superba. 2: characterization of solid state structure. Carbohydr Polym. 1992, 18: 43-49. 10.1016/0144-8617(92)90186-T.View ArticleGoogle Scholar
- Jang MK, Kong BG, Jeong YI, Lee CH, Nah JW: Physicochemical characterization of α-chitin, β-chitin, and γ-chitin separated from natural resources. J Polym Sci Part A: Polym Chem. 2004, 42: 3423-3432. 10.1002/pola.20176.View ArticleGoogle Scholar
- Gardner KH, Blackwell J: Refinement of the structure of β-chitin. Biopolymers. 1975, 14: 1581-1595. 10.1002/bip.1975.360140804.PubMedView ArticleGoogle Scholar
- Chatterjee S, Adhya M, Guha AK, Chatterjee BP: Chitosan from Mucor rouxii: production and physico-chemical characterization. Process Biochem. 2005, 40: 395-400. 10.1016/j.procbio.2004.01.025.View ArticleGoogle Scholar
- Peng T, Goosen MFA: Structural changes of pH-sensitive chitosan/polyether hydrogels in different pH solution. J Polym Sci A1. 1994, 32: 591-596. 10.1002/pola.1994.080320322.View ArticleGoogle Scholar
- Cárdenas G, Carbrera G, Taboada E, Miranda SP: Chitin characterization by SEM FTIR, XRD, and 13C cross polarization/mass angle spinning NMR. J Appl Polym Sci. 2004, 93: 1876-1885. 10.1002/app.20647.View ArticleGoogle Scholar
- Kaya M, Tozak KO, Baran T, Sezen G, Sargin I: Natural porous and nano fiber Chitin structure from Gammarus argaeus (Gammaridae Crustacea). Excli J. 2013, 12: 503-510.Google Scholar
- Kaya M, Sargin I, Tozak KO, Baran T, Erdogan S, Sezen G: Chitin extraction and characterization from Daphnia magna resting eggs. Int J Biol Macromol. 2013, 61: 459-464. 10.1016/j.ijbiomac.2013.08.016.PubMedView ArticleGoogle Scholar
- Yen MT, Yang JH, Mau JL: Physicochemical characterization of chitin and chitosan from crab shells. Carbohydr Polym. 2009, 75: 15-21. 10.1016/j.carbpol.2008.06.006.View ArticleGoogle Scholar
- Kucukgulmez A, Celik M, Yanar Y, Sen D, Polat H, Kadak AE: Physicochemical characterization of chitosan extracted from Metapenaeus stebbingi shells. Food Chem. 2011, 126: 1144-1148. 10.1016/j.foodchem.2010.11.148.View ArticleGoogle Scholar
- Yen MT, Mau JL: Selected physical properties of chitin prepared from shiitake stipes. Lwt - Food Sci Technol. 2007, 40: 558-563. 10.1016/j.lwt.2005.10.008.View ArticleGoogle Scholar
- Chan HY, Chen MH, Yuan GF: Fungal chitosan. Fungal Sci. 2001, 16: 39-52.Google Scholar
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