scholarly journals Isolation of papain-soluble collagen from the skin of snake-head fish (Channa striata)

2020 ◽  
pp. 87-93
Author(s):  
Andi Rahmayanti Ramli ◽  
Andi Rezky Annisa ◽  
Nur Alim Bahmid ◽  
Muhammad Dalvi Mustafa
Keyword(s):  
Fourier Transform ◽  
Moisture Content ◽  
Polyacrylamide Gel Electrophoresis ◽  
Fourier Transform Infrared ◽  
Helical Structure ◽  
Collagen Type I ◽  
Type I ◽  
Fish Skin ◽  
Soluble Collagen ◽  
Channa Striata

Snake-head fish (Channa striata) skin categorized a byproduct contains a higher concentration of collagen. The collagen can be extracted by using protease, which is known as Papain Soluble Collagen (PaSC). This study aimed to isolate the collagen from the snake-head fish skin using papain. The yield percentage and moisture content of PaSC in the skin was determined. Measurements using SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and Fourier transform infrared spectroscopy (FTIR) were performed to characterize the PaSC and its functional groups. The results showed that the yields and moisture content of PaSC were 8.9% and 6.07%, respectively. The PaSC characterized by two α-chains appeared as collagen type I. Fourier transform infrared (FTIR) spectra of PaSC confirmed a triple-helical structure of collagen. The results indicated that snake-head fish skin could be used as potential resources of collagen and papain can be used as an alternative affordable enzyme.

scholarly journals Characterization of Acid-Soluble Collagen from Food Processing By-Products of Snakehead Fish (Channa striata)

Processes ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 1188
Author(s):  
Thi Mong Thu Truong ◽  
Van Muoi Nguyen ◽  
Thanh Truc Tran ◽  
Thi Minh Thuy Le
Keyword(s):  
Acid Content ◽  
Type I Collagen ◽  
Type I ◽  
Fish Skin ◽  
Soluble Collagen ◽  
Acid Soluble Collagen ◽  
Imino Acid ◽  
Channa Striata ◽  
Α Helix ◽  
By Products

The isolation of acid-soluble collagen (ASC) from by-products of snakehead fish (Channa striata), including skin and the mixture of skin and scale, has been investigated. The recovery yield of fish skin ASC (13.6%) was higher than ASC from fish skin and scale (12.09%). Both ASCs were identified as type I collagen and showed maximal solubility at pH 2. Collagen samples from the mixture of skin and scale had higher imino acid content (226 residues/1000 residues) and lower wavenumber in the amide I and amide III region (1642 and 1203 cm−1, respectively) than the fish skin ASC (the imino acid content was 220 residues/1000 residues and the wavenumber in the amide I and amide III were 1663 and 1206 cm−1, respectively. The difference scanning calorimeter (DSC) showed higher thermal stability in ASC from the mixture of skin and scale (Td of 35.78 °C) than fish skin ASC (34.21 °C). From the result, the denaturation temperature of ASC had a close relationship with the content of imino acid as well as with the degradation of α-helix in amide I and III. These results suggest that collagen could be obtained effectively from snakehead fish by-products and has potential as a realistic alternative to mammalian collagens.

scholarly journals Characterization of Protease Soluble Collagen (PSC) From Milkfish Scales (Chanos chanos)

2019 ◽  
Vol 8 (3) ◽  
pp. 245-254
Author(s):  
Nia Lutfiana ◽  
◽  
Suharti Suharti ◽  
Evi Susanti ◽  
◽  
...  
Keyword(s):  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Collagen Type I ◽  
Differential Scanning Calorimetric ◽  
Type I ◽  
Denaturation Temperature ◽  
Soluble Collagen ◽  
Sds Page ◽  
Ft Ir

The aim of this study was to characterize protease soluble collagen (PSC) obtained from milkfish scales, extraction using protease from proteolytic bacteria HTcUM7.1 isolate. The characterization included Fourier Transform Infra Red (FT-IR) spectra, Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) profile, Field Emission Scanning Electron Microscopy (FESEM), denaturation temperature by Differential Scanning Calorimetric (DSC) and solubility. The resulting PSC from milkfish scales has white color, fiber with a length of about 20-60 µm, FTIR spectra and SDS-PAGE profile showed that PSC was collagen Type I and denaturation temperature was 145.48 °C, with maximum solubility at pH 1-3 and 1-2 % NaCl. Its high denaturation temperature value allows the collagen to be applied in the fields of medicines and cosmetics.

scholarly journals Extraction of collagen Type-I from snakehead fish skin (Channa striata) and synthesis of biopolymer for wound dressing

2019 ◽  
Author(s):  
Faris Bari Issains ◽  
Achmad Fauzi Trinanda ◽  
Alif Muhammad Basyir ◽  
Abel Benaya ◽  
Akhmad Herman Yuwono ◽  
...  
Keyword(s):  
Wound Dressing ◽  
Collagen Type ◽  
Collagen Type I ◽  
Type I ◽  
Fish Skin ◽  
Channa Striata

scholarly journals Comprehensive Assessment of Nile Tilapia Skin (Oreochromis niloticus) Collagen Hydrogels for Wound Dressings

Marine Drugs ◽  
2020 ◽  
Vol 18 (4) ◽  
pp. 178 ◽  
Author(s):  
Baosheng Ge ◽  
Haonan Wang ◽  
Jie Li ◽  
Hengheng Liu ◽  
Yonghao Yin ◽  
...  
Keyword(s):  
Wound Dressing ◽  
Type I Collagen ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Wound Dressings ◽  
Type I ◽  
Rheological Characterization ◽  
Scanning Calorimetry ◽  
Soluble Collagen ◽  
Collagen Hydrogels

Collagen plays an important role in the formation of extracellular matrix (ECM) and development/migration of cells and tissues. Here we report the preparation of collagen and collagen hydrogel from the skin of tilapia and an evaluation of their potential as a wound dressing for the treatment of refractory wounds. The acid-soluble collagen (ASC) and pepsin-soluble collagen (PSC) were extracted and characterized using sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), differential scanning calorimetry (DSC), circular dichroism (CD) and Fourier transform infrared spectroscopy (FTIR) analysis. Both ASC and PSC belong to type I collagen and have a complete triple helix structure, but PSC shows lower molecular weight and thermal stability, and has the inherent low antigenicity. Therefore, PSC was selected to prepare biomedical hydrogels using its self-aggregating properties. Rheological characterization showed that the mechanical strength of the hydrogels increased as the PSC content increased. Scanning electron microscope (SEM) analysis indicated that hydrogels could form a regular network structure at a suitable PSC content. Cytotoxicity experiments confirmed that hydrogels with different PSC content showed no significant toxicity to fibroblasts. Skin repair experiments and pathological analysis showed that the collagen hydrogels wound dressing could significantly accelerate the healing of deep second-degree burn wounds and the generation of new skin appendages, which can be used for treatment of various refractory wounds.

A Newly Identified Platelet and Megakaryocyte Lysyl Oxidase-Adhesion to Collagen Axis in Human Primary Myelofibrosis

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 3133-3133
Author(s):  
Alessandra Balduini ◽  
Vittorio Abbonante ◽  
Shinobu Matsuura ◽  
Vittorio Rosti ◽  
Katya Ravid
Keyword(s):  
Type I Collagen ◽  
Conflicts Of Interest ◽  
Lysyl Oxidase ◽  
Primary Myelofibrosis ◽  
Collagen Type I ◽  
Type I ◽  
Soluble Collagen ◽  
Peripheral Blood Cd34 ◽  
Acid Soluble Collagen

Abstract Controlling platelet function is central to management of various pathologies, including Primary Myelofibrosis (PMF), which is associated with increased incidence of thrombosis and cardiovascular disease. In recent studies we showed that the matrix cross-linking enzyme, Lysyl Oxidase (LOX) is elevated in platelets and megakartocytes of myelofibrotic mice, and transgenic upregulation of LOX increases platelet and megakaryocyte adhesion to monomeric type I collagen (preferred by alpha2β1 collagen receptors), and augments propensity for in vivo thrombosis. Here, we examined the relevance of these findings to human disease, by first determining platelet LOX level, as well as platelet and megakaryocyte adhesion to collagen using samples derived from PMF patients and matching controls. In analyzing 10 PMF platelet samples (5 males and 5 females; 6 JAK2V617F; 4 CALR mutations; age range 30-55; PMF grade 1-3), we found a nearly 20 fold upregulation of LOX expression compared to matching healthy controls (p<0.001). Intriguingly, there was a significant increase in adhesion (plt/mm2) and spreading (pixel2) of PMF platelets relative to control on monomeric, pepsinated acid soluble collagen (PSCI) (p<0.05), while no differences were observed between the samples on native triple helical acid soluble collagen type I collagen (ASCI). To examine the role of LOX in this phenotype, we treated control and PMF-derived human megakaryocytes, differentiated from peripheral blood CD34+ cells, grown in presence or not of LOX inhibitor, β-aminopropionitrile (BAPN) from day 2 of culture. Our preliminary data, based on a cohort of 2 controls and 5 PMF samples, demonstrated that although on ASCI megakaryocyte adhesion is not altered by BAPN treatment both in CTRL and PMF derived megakaryocytes, on PSCI the adhesion of PMF derived megakaryocytes was reduced by about a 50% by BAPN treatment, while the adhesion of CTRL derived MKs was not significantly affected. Taken together, we identified LOX level to be upregulated in human PMF platelets and megakaryocytes, and LOX activity to be important for PMF cells adhesion to collagen. These newly identified properties are highly relevant to megakaryocyte adhesion to the niche, and to platelet activation in PMF. Disclosures No relevant conflicts of interest to declare.

scholarly journals Preparation and Characterization of Thermally Stable Collagens from the Scales of Lizardfish (Synodus macrops)

Marine Drugs ◽  
2021 ◽  
Vol 19 (11) ◽  
pp. 597
Author(s):  
Junde Chen ◽  
Guangyu Wang ◽  
Yushuang Li
Keyword(s):  
Type I Collagen ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Type I ◽  
Salting Out ◽  
Soluble Collagen ◽  
Acid Soluble Collagen ◽  
Skin Collagen ◽  
Rat Tail

Marine collagen is gaining vast interest because of its high biocompatibility and lack of religious and social restrictions compared with collagen from terrestrial sources. In this study, lizardfish (Synodus macrops) scales were used to isolate acid-soluble collagen (ASC) and pepsin-soluble collagen (PSC). Both ASC and PSC were identified as type I collagen with intact triple-helix structures by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and spectroscopy. The ASC and PSC had high amino acids of 237 residues/1000 residues and 236 residues/1000 residues, respectively. Thus, the maximum transition temperature (Tmax) of ASC (43.2 °C) was higher than that of PSC (42.5 °C). Interestingly, the Tmax of both ASC and PSC was higher than that of rat tail collagen (39.4 °C) and calf skin collagen (35.0 °C), the terrestrial collagen. Solubility tests showed that both ASC and PSC exhibited high solubility in the acidic pH ranges. ASC was less susceptible to the “salting out” effect compared with PSC. Both collagen types were nontoxic to HaCaT and MC3T3-E1 cells, and ASC was associated with a higher cell viability than PSC. These results indicated that ASC from lizardfish scales could be an alternative to terrestrial sources of collagen, with potential for biomedical applications.

scholarly journals MOLECULAR STRUCTURE OF GELATIN EXTRACTED FROM PARROT (Scarus sp) FISH SCALES

2020 ◽  
Vol 8 (1) ◽  
pp. 15
Author(s):  
Jeszy Novianti Andakke ◽  
Inneke F M Rumengan ◽  
Hizkia H Y Nainggolan ◽  
Lasma R M E Parapat ◽  
Engel Pandey ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Fourier Transform ◽  
Moisture Content ◽  
Key Words ◽  
Triple Helix ◽  
Fourier Transform Infrared ◽  
Water Soluble ◽  
Wave Number ◽  
Fish Scales ◽  
Single Helix

One of the protein molecules of fish scales is water soluble gelatin. Gelatin of fish scales could be best substitute of commercial available gelatin which derived from porcine and bovine. The purpose of this study was to determine the molecular structure of gelatin extracted from marine fish scale using Fourier transform infrared (FTIR) analysis, and to obtain the moisture content, pH and yield of gelatin. Samples were prepared from the wet and dried scales. As for the standard gelatin, the gelatin of the two samples are characterized with several types of amide groups. The two gelatin samples were slight different in absorption of wave length for amide A, B, I, II and III groups indicating the instability of the functional groups which may influence viscosity and gel strength. For the wet scales derived gelatin, the wave number absorption was found to be 3412 cm-1 (amide A), 2421 cm-1 (amide B), 1653 cm-1 (amide I), 1400 cm-1 (amide II), and 1001 cm-1 (amide III), while for the dried scales derived gelatin was 3435 cm-1 (amide A), 2920 cm-1 (amide B), 1635 cm-1 (amide I), 1404 cm-1 (amide II), and 1036 cm-1 (amide III). The wave number absorption of amide III of gelatin is smaller than the one of collagen, because gelatin is in form of single helix, not triple helix. The wet scales derived and dried scales derived gelatin show the moisture content of 15.0% and 13.7%, and yield of 2.33% and 2.43%, .respectively. For both samples, the pH value was 7. Key words : gelatin, fish scales, molecule structure, moisture, yield, pH Abstrak Salah satu dari molekul protein sisik ikan adalah gelatin larut air. Gelatin sisik ikan dapat menjadi pengganti terbaik dari gelatin komersial yang tersedia yang berasal dari babi dan sapi. Tujuan dari penelitian ini adalah untuk menentukan struktur molekul gelatin yang diekstrak dari sisik ikan laut menggunakan Analisis FTIR (Fourier Transform Infrared), dan untuk mendapatkan kadar air, pH dan rendemen gelatin. Sampel disiapkan dari sisik basah dan sisik kering. Adapun standar gelatin, gelatin dari kedua sampel ditandai dengan beberapa jenis gugus amida. Kedua sampel gelatin sedikit berbeda dalam penyerapan panjang gelombang untuk amida A, B, I, II dan III yang menunjukkan ketidakstabilan kelompok fungsional yang dapat mempengaruhi viskositas dan kekuatan gel. Untuk gelatin sisik basah, panjang gelombang serapan ditemukan pada 3412 cm-1 (amida A), 2421 cm-1 (amida B), 1653 cm-1 (amida I), 1400 cm-1 (amida II), and 1001 cm-1 (amida III), sedangkan untuk gelatin sisik kering adalah 3435 cm-1 (amida A), 2920 cm-1 (amida B), 1635 cm-1 (amida I), 1404 cm-1 (amida II), and 1036 cm-1 (amida III). Panjang gelombang serapan amida III pada gelatin lebih kecil dibanding kolagen, sehingga gelatin berbentuk single helix, bukan triple helix. Gelatin sisik basah dan sisik kering mengadung kadar air 15,0% dan 13,7%, rendemen 2,33% and 2,43%, secara berturut-turut. Untuk kedua sampel memiliki nilai pH 7. Key words : gelatin, sisik ikan, struktur molekul, kadar air, rendemen, pH

Enhancement by Heparin of Affinity between Cold-Insoluble Globulin and Native Collagen Type III

1979 ◽  
Author(s):  
H. Hörmann ◽  
F. Jilek
Keyword(s):  
Collagen Type ◽  
Weight Ratio ◽  
Collagen Type I ◽  
Type I ◽  
Collagen Type Iii ◽  
Type Iii ◽  
Soluble Collagen ◽  
Native Collagen ◽  
Collagen Molecules ◽  
Cold Insoluble Globulin

Affinity between collagen and cold-insoluble globulin was measured by complexing soluble 125-J labelled collagen preparations with the globulin. Precipitates containing considerable activity were formed at 4°C and 22°C by denatured soluble collagen, type I and type III, but only little by native soluble collagen. The precipitation of native collagen, type III, by cold-insoluble globulin was enhanced by heparin. Under optimal conditions at a weight ratio or heparin and cold-insoluble globulin of about 1:1 up to 60% of the collagen applied was insolubilized. Native collagen, type I, was complexed far less effectively even in presence of heparin. Electronmicroscopic and precipitation experiments using 125-J labelled cold-insoluble globulin indicated that heparin might induce a partial conversion of cold-insoluble globulin to a fibrillar derivative which exhibited improved binding properties for the rod-like native collagen molecules. – Supported by Deutsche Forschungsgemeinschaft, Project Ho 740/1.

The Preparation and Characteristic Research of Keratin Powder Based on TCEP

2014 ◽  
Vol 1053 ◽  
pp. 438-443
Author(s):  
Jian Yong Liu ◽  
Jie Wang ◽  
Hao Ming Li
Keyword(s):  
Differential Scanning Calorimetry ◽  
Fourier Transform ◽  
Moisture Content ◽  
Helical Structure ◽  
Ftir Analysis ◽  
Dsc Analysis ◽  
Scanning Calorimetry ◽  
Β Sheet ◽  
Melting Peak Temperature ◽  
Wool Keratin

In this paper, the wool was pretreated by TCEP (Tris (2-carboxyethyl) phosphine) a certain time, and then prepared wool keratin powder by mechanical lapping. The characteristics of the keratin powder carried out by Fourier transform infrared (FTIR) and Differential scanning calorimetry (DSC). From the FTIR analysis, TCEP first role in α-helical structure of wool, making its decline, and then acting on β-sheet. From the DSC analysis, the melting peak temperature of α-crystalline with the time of TCEP effect on wool, presenting the trend of first increased and then drophave. Dissolved the keratin powder in 88% formic acid, then keratin films were maded.The characteristics of the keratin films were measured, the moisture content of keratin film increases with the time of wool treated with TCEP. And the dissolution rate and ultimate strength in line with the change of FTIR and DSC analysis results.

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