New Source of 3D Chitin Scaffolds: The Red Sea Demosponge Pseudoceratina arabica (Pseudoceratinidae, Verongiida)

The bioactive bromotyrosine-derived alkaloids and unique morphologically-defined fibrous skeleton of chitin origin have been found recently in marine demosponges of the order Verongiida. The sophisticated three-dimensional (3D) structure of skeletal chitinous scaffolds supported their use in biomedicine, tissue engineering as well as in diverse modern technologies. The goal of this study was the screening of new species of the order Verongiida to find another renewable source of naturally prefabricated 3D chitinous scaffolds. Special attention was paid to demosponge species, which could be farmed on large scale using marine aquaculture methods. In this study, the demosponge Pseudoceratina arabica collected in the coastal waters of the Egyptian Red Sea was examined as a potential source of chitin for the first time. Various bioanalytical tools including scanning electron microscopy (SEM), fluorescence microscopy, FTIR analysis, Calcofluor white staining, electrospray ionization mass spectrometry (ESI-MS), as well as a chitinase digestion assay were successfully used to confirm the discovery of α-chitin within the skeleton of P. arabica. The current finding should make an important contribution to the field of application of this verongiid sponge as a novel renewable source of biologically-active metabolites and chitin, which are important for development of the blue biotechnology especially in marine oriented biomedicine.

. The fragment of the dried specimens of P. arabica demosponge used in this study.

Results
Figure 2 clearly shows that the alkali treatment resulted in depigmented, protein-free, fibrous scaffolds with residual siliceous spicules and foreign, sandy microparticles within the fibers ( Figure  3). Observations of these contaminants into the NaOH-treated fragments of P. arabica support our previous suggestion about the allochronic origin of sponges from Pseudoceratinidae family [33].

Results
Figure 2 clearly shows that the alkali treatment resulted in depigmented, protein-free, fibrous scaffolds with residual siliceous spicules and foreign, sandy microparticles within the fibers (Figure 3). Observations of these contaminants into the NaOH-treated fragments of P. arabica support our previous suggestion about the allochronic origin of sponges from Pseudoceratinidae family [33].

Results
Figure 2 clearly shows that the alkali treatment resulted in depigmented, protein-free, fibrous scaffolds with residual siliceous spicules and foreign, sandy microparticles within the fibers ( Figure  3). Observations of these contaminants into the NaOH-treated fragments of P. arabica support our previous suggestion about the allochronic origin of sponges from Pseudoceratinidae family [33].   SEM microphotographs of the scaffolds isolated from P. arabica before ( Figure 4) and after ( Figure 5) HF-treatment show that only treatment using diluted HF water solution leads to dissolution and removal of sand microparticles as well as spicules and result in silica-free, pure, microfibers with high structural integrity, as observed before in other verongiid sponges [6,13,15,40] ( Figure 5). These results were also confirmed using light as well as fluorescent microscopy ( Figure 6). SEM microphotographs of the scaffolds isolated from P. arabica before ( Figure 4) and after ( Figure 5) HF-treatment show that only treatment using diluted HF water solution leads to dissolution and removal of sand microparticles as well as spicules and result in silica-free, pure, microfibers with high structural integrity, as observed before in other verongiid sponges [6,13,15,40] (Figure 5). These results were also confirmed using light as well as fluorescent microscopy ( Figure 6).     Typically, Calcofluor white staining (CFW) was used as the first stage of chitin identification in completely demineralized (including HF-based treatment) sponge skeletons. This fluorescent dye is commonly used for staining β-(1→3) and β-(1→4) linked polysaccharides including chitin. Consequently, after binding to polysaccharides, CFW dye exhibits bright blue light under UV excitations [41]. Examination of the scaffolds isolated from P. arabica after CFW staining using fluorescent microscopy demonstrate strong fluorescence under light exposure time as short as 1/4800 s (Figure 7 B). Similar conclusions were reported previously for chitin isolated from sponges of marine [6,10,15,32,33,40] as well as freshwater [12] origin and fossilized chitin-containing remains [11,41].
More precise methods were applied to study in details the presence and identification of chitin in isolated scaffolds. FTIR spectroscopy is considered as an effective technique for structural analysis Typically, Calcofluor white staining (CFW) was used as the first stage of chitin identification in completely demineralized (including HF-based treatment) sponge skeletons. This fluorescent dye is commonly used for staining β-(1→3) and β-(1→4) linked polysaccharides including chitin. Consequently, after binding to polysaccharides, CFW dye exhibits bright blue light under UV excitations [41].
Examination of the scaffolds isolated from P. arabica after CFW staining using fluorescent microscopy demonstrate strong fluorescence under light exposure time as short as 1/4800 s ( Figure 7B). Similar conclusions were reported previously for chitin isolated from sponges of marine [6,10,15,32,33,40] as well as freshwater [12] origin and fossilized chitin-containing remains [11,41]. Typically, Calcofluor white staining (CFW) was used as the first stage of chitin identification in completely demineralized (including HF-based treatment) sponge skeletons. This fluorescent dye is commonly used for staining β-(1→3) and β-(1→4) linked polysaccharides including chitin. Consequently, after binding to polysaccharides, CFW dye exhibits bright blue light under UV excitations [41]. Examination of the scaffolds isolated from P. arabica after CFW staining using fluorescent microscopy demonstrate strong fluorescence under light exposure time as short as 1/4800 s (Figure 7 B). Similar conclusions were reported previously for chitin isolated from sponges of marine [6,10,15,32,33,40] as well as freshwater [12] origin and fossilized chitin-containing remains [11,41].  More precise methods were applied to study in details the presence and identification of chitin in isolated scaffolds. FTIR spectroscopy is considered as an effective technique for structural analysis of different polysaccharides including chitin. Recently, FTIR analysis was successfully used to obtain information about of type of polymorph form of chitin [42].
The acquired FTIR spectra of demineralized scaffolds of P. arabica and standard α-chitin are presented in Figure 8. Between 1700 and 1500 cm −1 , the different signatures characteristic for chitin polymorphs were observed. In this amidic moiety region, the investigated sample showed strong band related to the stretching vibrations of C=O group characteristic for band I of the amidic moiety. This band, registered for studied sample, possessed twin peaks at 1651 and 1633 cm −1 , which is related with the presence of two types of carbonyl groups within the chitin chain, and it is also typical for α-chitin. The first peak derives from the specific intermolecular hydrogen bond of carbonyl group and hydroxymethyl group on the next chitin residue in the same chain. The second peak is a result of the intramolecular hydrogen bonds of carbonyl with the amide groups. Additionally, in the purified sponge chitin sample, as well as in the α-chitin standard, the characteristic intense band at v max 948 cm −1 which is referred to γCH x bond was observed. Moreover, the α-chitin characteristic band assigned to β-glycosidic bond at 895 cm −1 is well visible in the studied samples. However, it should be noted that the characteristic bands for CaCO 3 (855-876 cm −1 ) and SiO 2 (720 cm −1 ) were not observed in the spectrum of P. arabica, suggesting that procedure of chitin isolation resulted in chitin of high purity. Additionally, the comprehensive analysis of acquired spectra shows that recorded bands correspond with those referred in the α-chitin reference sample. of different polysaccharides including chitin. Recently, FTIR analysis was successfully used to obtain information about of type of polymorph form of chitin [42].
The acquired FTIR spectra of demineralized scaffolds of P. arabica and standard α-chitin are presented in Figure 8. Between 1700 and 1500 cm −1 , the different signatures characteristic for chitin polymorphs were observed. In this amidic moiety region, the investigated sample showed strong band related to the stretching vibrations of C=O group characteristic for band I of the amidic moiety. This band, registered for studied sample, possessed twin peaks at 1651 and 1633 cm −1 , which is related with the presence of two types of carbonyl groups within the chitin chain, and it is also typical for αchitin. The first peak derives from the specific intermolecular hydrogen bond of carbonyl group and hydroxymethyl group on the next chitin residue in the same chain. The second peak is a result of the intramolecular hydrogen bonds of carbonyl with the amide groups. Additionally, in the purified sponge chitin sample, as well as in the α-chitin standard, the characteristic intense band at vmax 948 cm −1 which is referred to γCHx bond was observed. Moreover, the α-chitin characteristic band assigned to β-glycosidic bond at 895 cm -1 is well visible in the studied samples. However, it should be noted that the characteristic bands for CaCO3 (855-876 cm -1 ) and SiO2 (720 cm -1 ) were not observed in the spectrum of P. arabica, suggesting that procedure of chitin isolation resulted in chitin of high purity. Additionally, the comprehensive analysis of acquired spectra shows that recorded bands correspond with those referred in the α-chitin reference sample.  Figure 9 shows the Raman spectrum of chitin isolated from P. arabica compared with the spectrum of the α-chitin reference. Characteristic bands for α-chitin can be found in the spectrum of the isolated chitin within the spectral resolution of the measurement. The existence of two bands characteristic to amine band I at vmax 1657 and 1624 cm -1 as well as intense band related to the βglycosidic bond at vmax 895 cm -1 clearly indicate that chitin isolated from P. arabica is of α isomorph.  Figure 9 shows the Raman spectrum of chitin isolated from P. arabica compared with the spectrum of the α-chitin reference. Characteristic bands for α-chitin can be found in the spectrum of the isolated chitin within the spectral resolution of the measurement. The existence of two bands characteristic to amine band I at v max 1657 and 1624 cm −1 as well as intense band related to the β-glycosidic bond at v max 895 cm −1 clearly indicate that chitin isolated from P. arabica is of α isomorph. Moreover, the bands in the spectrum are in good agreement with previously published data [5,10,43,44].

Mar. Drugs 2018, 16, x 9 of 17
Moreover, the bands in the spectrum are in good agreement with previously published data [5,10,43,44]. Previously, in order to confirm the presence of chitin in diverse sponges, the chitinase digestion test has been successfully applied [6,10,15,32,33,40]. This enzyme has unique ability to decompose chitin into low-molecular oligomers such as N-acetyl-D-glucosamine (GlcNAc). Therefore, the action of chitinase leads to the loss of chitin integrity and the release of residual chitin microfibers of steadily decreasing size. The changes in the structure of treated fibers can be observed using light microscopy ( Figure 10). This test is unequivocal and provides additional confirmation of the successful chitin isolation from the sponge under study here.  Previously, in order to confirm the presence of chitin in diverse sponges, the chitinase digestion test has been successfully applied [6,10,15,32,33,40]. This enzyme has unique ability to decompose chitin into low-molecular oligomers such as N-acetyl-D-glucosamine (GlcNAc). Therefore, the action of chitinase leads to the loss of chitin integrity and the release of residual chitin microfibers of steadily decreasing size. The changes in the structure of treated fibers can be observed using light microscopy ( Figure 10). This test is unequivocal and provides additional confirmation of the successful chitin isolation from the sponge under study here. Moreover, the bands in the spectrum are in good agreement with previously published data [5,10,43,44]. Previously, in order to confirm the presence of chitin in diverse sponges, the chitinase digestion test has been successfully applied [6,10,15,32,33,40]. This enzyme has unique ability to decompose chitin into low-molecular oligomers such as N-acetyl-D-glucosamine (GlcNAc). Therefore, the action of chitinase leads to the loss of chitin integrity and the release of residual chitin microfibers of steadily decreasing size. The changes in the structure of treated fibers can be observed using light microscopy ( Figure 10). This test is unequivocal and provides additional confirmation of the successful chitin isolation from the sponge under study here. D-glucosamine (dGlcN) is the product of chitin's acidic hydrolysis which can be readily identified by electrospray-ionization mass spectroscopy (ESI-MS) measurements. Thus, ESI-MS spectroscopy becomes a standard method for chitin identification which usability was shown in complex organisms [40,45,46] and even in 505-million-year-old chitin-containing fossil remnants [47]. D-glucosamine (dGlcN) is the product of chitin's acidic hydrolysis which can be readily identified by electrospray-ionization mass spectroscopy (ESI-MS) measurements. Thus, ESI-MS spectroscopy becomes a standard method for chitin identification which usability was shown in complex organisms [40,45,46] and even in 505-million-year-old chitin-containing fossil remnants [47]. In

Isolation of Chitin from P. Arabica
The isolation of chitin scaffolds from P. arabica (Figure 1) was carried out according to our previous reports [12,40,52]. The methodology consists of four steps ( Figure 12): first, the skeleton of P. arabica was incubated in deionized water at room temperature for one hour to remove possible water-soluble sediment particles and salts. In the second step, the samples were treated with 3 M HCl at room temperature for 6 h in order to eliminate possible residual calcium carbonate-based debris (micro fragments of crustacean carapaces and mollusc shells) from the skeleton of P. arabica. Afterwards, the samples were washed several times with deionized water until achieving a pH of 6.5 followed by treatment with 2.5 M NaOH at 37 °C for 72 h to remove pigments and proteins. Due to the observation of the foreign spicules and their fragments in the samples after 72 h of alkali treatment, additional desilicification was needed. Consequently, alkali-treated samples were accurately rinsed with deionized water and stored in a plastic vessel containing appropriate amount of 10% hydrofluoric acid (HF) solution (step four). The vessel was covered in order to prevent the evaporation of HF. The desilicification process was conducted at room temperature for 12 h. The influence of alkaline and strong acidic treatments on the structure of skeleton of the studied sponge was investigated using stereo, white light and fluorescence microscopy. Finally, the isolated material was washed several times with deionized water up to a pH level of 6.5. The fibrous translucent scaffolds ( Figure 2) were placed into 250 ml large GLS 80 Duran glass bottles containing deionized water and stored at 4 °C for further analyses.

Light and Fluorescent Microscopy Analyses and Imaging
Collected sponge samples and isolated chitinous scaffolds were observed using BZ-9000 microscope (Keyence, Osaka, Japan) in the light as well as in the fluorescent microscopy modus.

Scanning Electron Microscopy Analysis
The morphology and microstructure of isolated and purified chitinous scaffolds, as well as untreated samples of P. arabica, were studied on the basis of SEM images using a Philips ESEM XL 30 scanning electron microscope (FEI Company, Peabody, MA, USA). Before analysis, samples were covered with a carbon layer for one minute using an Edwards S150B sputter coater (BOC Edwards, Wilmington, MA, USA).

Calcofluor White Staining Test
Due to the fact that Calcofluor White (Fluorescent Brightener M2R, Sigma-Aldrich, Taufkirchen, Germany) exhibits enhanced fluorescence after binding to chitin [53,54], this staining method was applied to investigate the location of chitin in the completely purified fibers of P. arabica. The selected chitinous fibers were soaked in 0.1 M KOH-glycerine-water solution and few drops of the 0.1% CFW solution were added. This mixture was incubated for 3 h in darkness, washed several times with

Discussion
Seas and oceans are a huge source of various invertebrate animals with potential to be used in biomedicine. For this reason, these organisms are frequently being tested for the presence of various useful products (unique secondary metabolites, biopolymers and biological materials), and many of them have been found in marine sponges. The order Verongiida has been recognized to be divided into four families, which differ in the structure and composition of skeletal fibers [48,49]. The largest verongiid family is Aplysinidae (52 species from three genera: Aiolochroia, Aplysina, and Verongula). This family is characterized by an anastomosing fiber skeleton with both pith and bark elements. The second largest verongiid family is Ianthellidae (21 species in four genera: Anomoianthella, Hexadella, Ianthella, and Vansoestia). The presence of eurypylous choanocyte chambers is a feature distinguishing this family from the others verongiids. Aplysinellidae includes 17 species in three genera (Aplysinella, Porphyra, and Suberea) with dendritic fiber skeleton possessing both pith and bark elements, which

Discussion
Seas and oceans are a huge source of various invertebrate animals with potential to be used in biomedicine. For this reason, these organisms are frequently being tested for the presence of various useful products (unique secondary metabolites, biopolymers and biological materials), and many of them have been found in marine sponges. The order Verongiida has been recognized to be divided into four families, which differ in the structure and composition of skeletal fibers [48,49]. The largest verongiid family is Aplysinidae (52 species from three genera: Aiolochroia, Aplysina, and Verongula). This family is characterized by an anastomosing fiber skeleton with both pith and bark elements. The second largest verongiid family is Ianthellidae (21 species in four genera: Anomoianthella, Hexadella, Ianthella, and Vansoestia). The presence of eurypylous choanocyte chambers is a feature distinguishing this family from the others verongiids. Aplysinellidae includes 17 species in three genera (Aplysinella, Porphyra, and Suberea) with dendritic fiber skeleton possessing both pith and bark elements, which are typical morphological features characteristic for representatives of this family. The verongiid P. arabica (Keller, 1889) that has been investigated in this study belongs to the family Pseudoceratinidae, which is currently including four species representing the only genus Pseudoceratina. Representatives of this family are characterized by a dendritic fiber skeleton with only pith elements. Interestingly, sponges of the genus Pseudoceratina are assumedly the richest sources of pharmacologically active alkaloids with diverse chemical skeletons within the order Verongiida [33]. Among various secondary metabolites isolated from Pseudoceratina species are: moloka'iamine derivatives, phenolic halogenated compounds, psammaplysins, pseudoceratinamide A and B, ceratinines, moloka'iakitamide, aplysterol, and aplysamine [33]. To date, a variety of secondary metabolites obtained from P. arabica have been purified using the solvent extraction method. Surprisingly, there are no literature reports on the extraction of these metabolites using the alkaline-based solution as well as about structural stability of such biomolecules at pH above 7. Alkaline stepwise extraction procedures were recently reported as effective methods for isolation of chitin-based scaffolds with bromotyrosines from other representatives of the order Verongiida and to "squeeze the full potential" of marine sponges [39]. However, it is necessary to prove, the pharmacological and biotechnological potential of the Red Sea verongiid sponges especially because of the recently published intriguing results concerning anti-tumorigenic and anti-metastatic activity of Aeroplysinin-1 which is one of the main bromotyrosine derivatives extracted from Verongiida [34]. All Verongiida sponge samples analyzed until now were found to exhibit a chitin-based scaffold, and here it was proved that P. arabica is the new example of chitin-containing sponge from this order. Apart from the bioactive metabolites of P. arabica, which are excellently described in the literature, here it was strongly demonstrated that this marine sponge can be effectively used also as a source of naturally prefabricated 3D chitinous scaffold with open-pore structure. Unfortunately, there is still lack of information concerning the interrelationships between the secondary metabolites and chitinous skeleton of P. arabica, especially with respect to their localization within so called spherulous cells. However, it known that spherulous cells are rich on bromotyrosines and have been found within skeletal fibres of verongiids [50]. The questions about the role of bromotyrosines in regeneration of chitinous skeleton as well as the growth rate of this species are still open. However, these data are crucial for the future estimation of the biotechnological, biomedical and pharmaceutical potential of P. arabica in the region.
It is worth to mention that, the 3D macroporous biomaterials of sponge origin gain a particular interest in tissue engineering, water purification, catalysis, and electrochemistry [51]. Preliminary research done with the use of corresponding 3D chitinous-scaffolds isolated from A. aerophoba [17] and Ianthella basta [18] confirm their biocompatibility with human mesenchymal stromal cells; supporting their adhesion, viability, growth, and proliferation. Additional, useful features of chitinous scaffolds of poriferan origin are their simplicity and ease of isolation. Calculated swelling capacity for chitinous matrices isolated from P. arabica is equal to 255 ± 8%. There are no doubts that comparative studies on interconnected porosity and swelling ability between chitinous matrices of P. arabica and that from other verongiid species [17,18] should be carried out. Consequently, the discovery of chitin in other members of the genus Pseudoceratina would be the next stage in the evaluation of the possibility to accept these organisms as a new source of 3D chitin scaffolds with macroporosity which range between 150-350 µm for biomedical applications. We suggest that the opportunity for ex situ cultivation of P. arabica can be an important advantage, which enables the use of this sponge for large scale applications in diverse advanced technologies.

Collection of Samples
Specimens of marine sponge Pseudoceratina arabica (Keller, 1889) (Porifera: Demospongiae: Verongiida: Pseudoceratinidae) described initially as Psammaplysilla arabica Keller, 1889 were collected by hands using SCUBA from the southern part of the Egyptian Hurghada (N 27 • 02 46.8" E 33 • 54 21.4") in July 2017 at depths up to 25 m. The yellowish green encrusting sponge with its conulose surface measuring about 1-2 cm thick. The preserved sponge in ethanol is completely black in color with dark-discolored ethanol. The conules on the sponge surface are bluntly rounded in shape, compressible and rubbery. The individual conules measure about 2-5 mm. The sponge skeleton consists of irregular and scattered fibers composed of pith. The outline and branching were irregular with thickness measuring between 80 and 300 µm. The sponge is similar to the sample collected in Red Sea from Eritrea. The sponge voucher (10.0 × 4.0 × 1.0 cm) was kept in the Zoological Museum of the University of Amsterdam with reference no. 17951. A similar specimen of the sponge was kept at Suez Canal University with collection reference DY-61. Collected specimens were kept on ice after collection. After returning to our laboratory, the specimens were freeze-dried ( Figure 1) and transferred to the bioanalytical laboratories at TU Bergakademie Freiberg (Freiberg, Germany).

Isolation of Chitin from P. Arabica
The isolation of chitin scaffolds from P. arabica (Figure 1) was carried out according to our previous reports [12,40,52]. The methodology consists of four steps ( Figure 11): first, the skeleton of P. arabica was incubated in deionized water at room temperature for one hour to remove possible water-soluble sediment particles and salts. In the second step, the samples were treated with 3 M HCl at room temperature for 6 h in order to eliminate possible residual calcium carbonate-based debris (micro fragments of crustacean carapaces and mollusc shells) from the skeleton of P. arabica. Afterwards, the samples were washed several times with deionized water until achieving a pH of 6.5 followed by treatment with 2.5 M NaOH at 37 • C for 72 h to remove pigments and proteins. Due to the observation of the foreign spicules and their fragments in the samples after 72 h of alkali treatment, additional desilicification was needed. Consequently, alkali-treated samples were accurately rinsed with deionized water and stored in a plastic vessel containing appropriate amount of 10% hydrofluoric acid (HF) solution (step four). The vessel was covered in order to prevent the evaporation of HF. The desilicification process was conducted at room temperature for 12 h. The influence of alkaline and strong acidic treatments on the structure of skeleton of the studied sponge was investigated using stereo, white light and fluorescence microscopy. Finally, the isolated material was washed several times with deionized water up to a pH level of 6.5. The fibrous translucent scaffolds ( Figure 2) were placed into 250 mL large GLS 80 Duran glass bottles containing deionized water and stored at 4 • C for further analyses.

Light and Fluorescent Microscopy Analyses and Imaging
Collected sponge samples and isolated chitinous scaffolds were observed using BZ-9000 microscope (Keyence, Osaka, Japan) in the light as well as in the fluorescent microscopy modus.

Scanning Electron Microscopy Analysis
The morphology and microstructure of isolated and purified chitinous scaffolds, as well as untreated samples of P. arabica, were studied on the basis of SEM images using a Philips ESEM XL 30 scanning electron microscope (FEI Company, Peabody, MA, USA). Before analysis, samples were covered with a carbon layer for one minute using an Edwards S150B sputter coater (BOC Edwards, Wilmington, MA, USA).

Calcofluor White Staining Test
Due to the fact that Calcofluor White (Fluorescent Brightener M2R, Sigma-Aldrich, Taufkirchen, Germany) exhibits enhanced fluorescence after binding to chitin [53,54], this staining method was applied to investigate the location of chitin in the completely purified fibers of P. arabica. The selected chitinous fibers were soaked in 0.1 M KOH-glycerine-water solution and few drops of the 0.1% CFW solution were added. This mixture was incubated for 3 h in darkness, washed several times with demineralized water, dried at room temperature and examined using BZ-9000 microscope (Keyence, Osaka, Japan).

FTIR and Raman Spectroscopy
FTIR spectra of chitinous scaffolds were acquired using a Nicolet 210c FTIR spectrometer. The samples were analysed using the ATR system with resolution equals 4 cm −1 . A micro-Raman system composed by a spectrometer (RamanRxn1™, Kaiser Optical Systems Inc., Ann Arbor, MI, USA), a 785 nm excitation laser diode (Invictus 785, Kaiser Optical Systems Inc., Ann Arbor, MI, USA) and an upright microscope (DM2500 P, Leica Microsystems GmbH, Wetzlar, Germany) was used to acquire the Raman spectra from the sample surface. Each spectrum was registered in the range 150-3250 cm −1 with resolution of 4 cm −1 , using a total acquisition time of 80 s. The fluorescence background was subtracted in MATLAB (MathWorks Inc., Natick, MA, USA) with a baseline procedure.

Chitinase Digestion Test
Yatalase®from culture supernatants of Corynebacterium sp. OZ-21 (Cosmo Bio, Tokyo, Japan) was used for the digestion test. Yatalase is a complex enzyme, consisting mainly of chitinase, chitobiase and β-1,3-glucanase. One unit of this enzyme released one µmol of N-acetylglucosamine from 0.5% chitin solution and 1 µmol of p-nitrophenol from p-nitrophenyl-N-acetyl-β-D-glucosaminide solution in 1 min at 37 • C and pH 6.0. The selected, completely demineralized chitinous scaffolds of P. arabica ( Figure 3) were incubated in an enzyme solution containing 10 mg/mL Yatalase dissolved in phosphate buffer at pH 6.0 for 2 h. The progress of digestion was monitored under light microscopy using BZ-9000 microscope (Keyence, Osaka, Japan).

Estimation of N-Acetyl-D-Glucosamine (NAG) Content and Electrospray Ionization Mass Spectrometry (ESI-MS)
The Morgan-Elson assay was used in order to evaluate the N-acetyl-D-glucosamine released after chitinase treatment, as described previously. For more details see [6,11,12].
Sample preparation for the ESI-MS analysis was performed by the hydrolysis of organic matrixes obtained after HF-treatment of the biological samples in 6M HCl (24 h at 90 • C). The samples, after HCl hydrolysis were filtrated with a 0.4 micron filter and freeze-dried in order to remove any excess HCl. The standard D-glucosamine as a control was purchased from Sigma (Sigma-Aldrich, Taufkirchen, Germany Both the commercial standard and the prepared sample were dissolved in water before ESI-MS analysis. ESI-MS measurements were performed on an Agilent Technologies 6230 TOF LC/MS spectrometer (Applied Biosystems, Foster City, CA, USA) in line as a detector in the analytical HPLC instrument. Nitrogen was used as the nebulizing and desolation gas.

Conclusions
The results of this investigation showed the need to develop new, simultaneous, more effective methods of extraction of both biologically active compounds and chitinous scaffolds from P. arabica and other species. The possibility of farming of Pseudoceratina species from primmorph-based cultures and under marine ranching conditions possesses high potential for advanced blue biotechnology. Due to the fact that, the P. arabica species live at low depths (around 10 m) development of a new method for their aquaculture in tropical areas become very attractive from the industrial and economical point of view. It is already confirmed that chitinous scaffolds isolated from representatives of the order Verongiida are lucrative for the development of regenerative medicine. Further research could also be conducted to determine the possibility of technological application of chitinous scaffolds of P. arabica origin as advanced 3D composite materials under conditions of extreme biomimetics or adsorbents. We suggest that this study will trigger the future research dedicated to both (i) discovery of chitin within other representatives of the family Pseudoceratinidae (ii) and their utilization in modern technologies improving the quality of human life and health. Funding: This work was partially supported by DFG Project HE 394/3-2 (Germany) and PUT Research Grant no. 03/32/DSMK/0810 (Poland). Marcin Wysokowski was supported by Foundation for Polish Science-START 097.2017 and SoniaŻółtowska-Aksamitowska was supported by DAAD as well as Erasmus Plus programs. A special thanks for technical assistance and discussions goes to BromMarin GmbH and INTIB GmbH (Germany). There was no additional external funding received for this study.

Conflicts of Interest:
The authors declare no conflict of interest.