• Food Science and Biotechnology
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• 제16권4호
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• pp.549-556
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• 2007

The study was carried out to examine on the refiner discharge from Alaska pollock as a collagen resource by characterizing biochemical and functional properties of collagen. The refiner discharge from Alaska pollock surimi manufacturing was a good resource for collagen extraction according to the results of total protein, heavy metal, volatile basic nitrogen, collagen content, amino acid composition, and thermal denaturation temperature (TDT). TDT of acid soluble collagen from refiner discharge showed $20.7^{\circ}C$, which was similar to that of collagen from Alaska pollock muscle and was higher than that of collagen from Alaska pollock skin. TDT of acid-soluble collagen from refiner discharge was, however, lower than those of skin collagens from warm fish and land animal. Acid-soluble collagen from refiner discharge of Alaska pollock could be used as a functional ingredient for food and industrial applications according to the results of water and oil absorption capacities, and emulsion properties. In addition, if the thermal stability of the acid-soluble collagens is improved, collagen from refiner discharge from Alaska pollock could be more effectively used.

• 한국식품저장유통학회지
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• 제17권1호
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• pp.91-99
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• 2010

상어의 껍질과 육 조직으로부터 산 (citric acid) 가용성 콜라겐 (ASC)과 pepsin 가용성 콜라겐 (PSC)의 추출 및 탈색조건을 조사하였다. 비 콜라겐 단백질을 제거하기 위한 적정 NaOH 농도는 0.3 N이었으며 처리시간은 9시간이었다. 상어껍질의 탈색은 생 원료에 대하여 10배량의 0.48% sodium hypochlorite로 60분간 처리하는 것이 적절하였다. ASC 및 PSC의 추출시 산의 적정농도는 각각 0.3 M 및 0.1 M이었고, 추출시간은 각각 72시간 및 24시간 이었다. 산가용성 콜라겐인 ASSC (citric acid soluble shark skin collagen)와 ASMC (citric acid soluble shark muscle collagen), pepsin 가용성 콜라겐인 PSSC(pepsin and citric soluble shark skin collagen)와 PSMC (pepsin soluble shark muscle collagen)에 함유된 총 단백질 함량은 각각 88.66, 83.09, 90.33 및 84.81% (dry basis)이었으며 시판 표준 콜라겐의 88.86%와 대등하였다. Hydroxyproline의 함량으로부터 산출한 순 콜라겐 함량은 ASC에서는 25.70~70.31%, PSC에서는 32.94~83.09%이었다. 상어육과 껍질 (dry basis) 100 g으로부터 얻을 수 있는 콜라겐의 수율은 ASC는 53.85~57.22%, PSC는 20.81~23.28%이었다.

• 한국식품과학회지
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• 제27권4호
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• pp.576-581
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• 1995

피부조직에서 추출한 콜라겐의 유동특성을 검토하여 콜라겐을 효율적으로 활용할 수 있는 기초자료를 얻고자 하였다. 콜라겐의 점도는 동물의 나이와 성(sex), 콜라겐 종류에 따라 차이를 보였다. 즉, 주령에 따라서는 콜라겐의 종류에 관계없이 $6{\sim}12$주령의 것이 비교적 높게 나타났으며, 동일 주령에서는 수컷의 점도보다 암컷의 점도가, 그리고 불용성 콜라겐의 점도보다 산가용성 콜라겐의 점도가 높게 나타났다. 콜라겐 용액은 Bingham plastic 및 thixotropic 유체의 특성을 나타냈으며, 온도, pH, 에탄올 농도 및 콜라겐 농도에 따라 점도 변화가 뚜렷하게 나타났다. 즉, 콜라겐 농도를 6%까지 높일 경우 콜라겐 용액의 점조도는 직선적으로 증가하는 경향(산가용성 콜라겐 r=0.972, 불용성 콜라겐 r=0.957)을 나타냈는데, 산가용성 콜라겐의 증가속도가 불용성 콜라겐의 경우보다 높게 나타났다. 온도 증가에 따라 콜라겐 용액의 점조도는 감소하였으며 특히, 산가용성 콜라겐에서는 $30{\sim}40^{\circ}C$ 온도구간에서 점조도가 급격히 감소하였다. pH에 따라 산가용성 콜라겐의 점조도는 pH 6에서 최대치를 보였고, pH 10 부근에서 다시 증가하는 biphasic 현상을 나타냈으나, 불용성 콜라겐의 경우는 pH에 큰 영향을 받지 않았다. 에탄올 농도에 따른 산가용성 콜라겐과 불용성 콜라겐의 점조도는 에탄올 농도 $40{\sim}60%$ 수준에서 높게 나타났다.

• Fisheries and Aquatic Sciences
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• 제21권4호
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• pp.7.1-7.8
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• 2018

In this study, we isolated and characterized the acid-soluble skin collagen of Pacific bluefin tuna (PBT, Thunnus orientalis). The PBT skin collagen was composed of two ${\alpha}$ chains (${\alpha}1$ and ${\alpha}2$) and one ${\beta}$ chain. The denaturation temperature of PBT collagen was low although it was rich in proline and hydroxyproline. The primary structure of PBT skin collagen was almost identical to that of calf and salmon skin collagen; however, it differed with respect to the epitope recognition of the antibody against salmon type I collagen. These results suggest that the primary structure of skin collagen was highly conserved among animal species, although partial sequences that included the epitope structure differed among collagens.

• 한국식품영양과학회지
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• 제27권2호
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• pp.305-312
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• 1998

Normal tensile strength in collagen fibrils is due to intermolecular and intramolecular crosslinks which are known to be altered in aging. Pyridinoline, a mature crosslink which is stable and nonreducible, is derived from two hydroxyallysine and one hydroxylysine residues of collagen fibrils. The excess formation of pyridinoline in collagen is associated with making the tissue stiffer, less soluble and less digestible by enzymes. Lysyl oxidase is the enzyme that initiates the biosynthesis or crosslinks in collagen by catalyzing the oxidative deamination of the lysyl and hydroxylysyl residues in these molecules, and its activity is inhibited by $\beta$-aminopropionitrile(BAPN). Our previous work demonstrated that the pyridinoline content of bone collagen significantly was increased during incubation for 5 weeks at 37$^{\circ}C$ invitro, but it was diecrased by the addition of ascorbic acdi(AsA). In this study, we clarified the specific action of AsA in aging process in vitro enzymatic reaction.

• 한국식품영양과학회지
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• 제26권3호
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• pp.501-506
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• 1997

As pyridinoline is one of the predominant cross-lins in a mature collagen, pyridinoline formation may be an essential step during the growth process to obtain normal mechanical strength in collagen fibrils. However, the excess formation of pyridinoline in collagen will probably make the tissue stiffer, less soluble and less digestible by enzymes. We investigated the changes of pyridinoline of bone collagen and the role of ascforbic acid(AsA) on the formation of pyridinoline. The pyridinoline content of bone collagen significantly increased during incubation for 1~5 weeks at 37$^{\circ}C$ in vitro. The addition of AsA decreased pyridinoline to half the amount found in controls with 5 week incubation. When dehydroascorbic acid(DHA) and L-2, 3-diketogulonic acid (DKG), the oxidative products of AsA, were supplemented to bone collagen solution instead of AsA, the content of pyridinoline in bone collagen was about 80% or 70% that of controls, respectively. These results suggest that pyridinoline content decreases by the addition of AsA in vitro. Furthermore, it was shown that AsA in oxidized from also affected the formation of pyridinoline.

• 한국식품저장유통학회지
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• 제16권3호
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• pp.419-426
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• 2009

상어 collagens(SC)(ASSC: 산가용성 껍질 collagen, ASMC: 산가용성 육 collagen, PSSC: pepsin 가용성 껍질 collagen, PSMC: pepsin 가용성 육 collagen)의 항산화성, 항균성, tyrosinase 및 elstase 저해활성을 표품(시판 marine collagen)과 비교하였다. SC($1{\sim}5\;mg/mL$)의 전자공여능은 $14.91{\sim}17.21%$로 표품의 $4.82{\sim}5.48%$에 비하여 $3.0{\sim}3.6$배가 높았다. SC($5{\sim}80\;mg/mL$)의 SOD활성은 4.67${\sim}37.28%$로 STMC 보다 $1.9{\sim}5.9$배가 높았다. SC의 S. aureus와 S. enteritidis에 대한 최소저해농도(MIC)는 $5{\mu}g$/disc로 표품의 $200{\mu}g$/disc보다 현저하게 낮았다. E. coli에 대한 MIC는 ASSC 및 ASMC에서는 $200{\mu}g$/disc인 반면 PSSC 및 PSMC는 $100{\mu}g$/disc이었으며 표품에서는 항균활성이 없었다. S. aureus에 대한 항균력은 PSMC가, S. enteritidis에 대한 항균력은 ASMC가, E. coli에 대한 항균력은 PSMC가 가장 높았다. SC($3{\sim}5\;mg/mL$)의 tyrosinase 저해활성은 $58.95{\sim}98.16%$로 표품의 $17.67{\sim}26.25%$보다 $3.34{\sim}3.74$배가 높았다. SC의 elastase 저해활성은 농도가 0.5 mg/mL에서 1 mg/mL으로 높아짐에 따라 비례적으로 증가하였고 1 mg/mL에서의 활성도는 $53.33{\sim}80.00%$로 STMC의 50.67% 보다 높았으며 PSSC에서 가장 높은 저해활성을 나타내었다. 산 및 pepsin 가용성의 모든 상어 collagen은 STMC에 비하여 $1.1{\sim}4.0$배의 높은 활성을 나타내었다. 이상의 결과 상어 collagens은 시판 marine collagen보다 항산화성, 항균성, tyrosinase 및 elastase 저해활성이 우수하여 새로운 기능성 소재로서의 활용성이 기대된다.

• Fisheries and Aquatic Sciences
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• 제24권12호
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• pp.406-414
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• 2021

The objective of this study was to investigate the yield and characteristics of collagen protein extracted from the muscle of four different species of mantis shrimp: Miyakella nepa, Harpiosquilla harpax, Erugosquilla woodmasoni, and Odontodactylus cultrifer. Mantis shrimp muscle was extracted by using a pepsin-solubilization technique, with 0.5 M acetic acid and 5% pepsin enzyme. The highest collagen yield was from M. nepa muscle (0.478 ± 0.06%), which was significantly greater (p < 0.05) than that from H. harpax, O. cultrifer, and E. woodmasoni (0.313 ± 0.03%, 0.123 ± 0.02%, and 0.015 ± 0.00%, respectively). The freeze-dried collagen appeared as thin fibers, and formed an opaque film. The pepsin-soluble collagen (PSC) from four mantis shrimp species was analyzed by gel electrophoresis. The results showed that all species of mantis shrimp contained type I collagen, consisting of β, α1, and α2 subunits with average molecular weights of 250, 145, and 118 kDa, respectively. The study of the solubility of collagen showed that, for NaCl, collagen had the highest relative solubility in 2% NaCl (80.20 ± 4.95%). In contrast, the solubility decreased at higher NaCl concentrations. However, in terms of pH, collagen had the highest relative solubility at pH 3 (91.32 ± 5.14%), and its solubility decreased at higher pH. FT-IR spectroscopy was used to compare the collagen with a model compound. Five wavenumbers in the spectrum for model collagen were identified: Amide A (3,406-3,421 cm^-1), amide B (2,916-2,940 cm^-1), amide I (1,639-1,640 cm^-1), amide II (1,539-1,570 cm^-1), and amide III (1,234-1,250 cm^-1).

• 한국수산과학회지
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• 제42권6호
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• pp.574-579
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• 2009

Acid- and pepsin-solubilized collagens were extracted from the skin of shark (Isurus oxyrinchus) and their physicochemical properties were characterized by amino acid analysis, SDS-PAGE, the composition of collagen types, solubility and denaturation temperature. Acid - and pepsin-solubilized collagens from shark skin had an imino acid of 188.8 and 186.2 residues/1,000 amino acids, respectively. SDS-PAGE showed two different${\alpha}$ chains ($\alpha1$ and $\alpha2$) and $\beta$-component. The component ratio of type I and V was 10:1, and the type III was not found. Solubility of acid-soluble collagen was low in the range of pH 6.0 to pH 11.0. On the other hand, pepsin-solubilized collagen showed a low solubility in the range of pH 7.0-9.0. Temperature for denaturation of acid- and pepsin-solubilized collagens were $25^{\circ}C$ and $27^{\circ}C$, respectively.

• Animal Bioscience
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• 제36권6호
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• pp.953-961
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• 2023

Objective: This study aimed to investigate the effect of dorsal cranial myopathy (DCM) on chicken meat quality. Methods: Sixty-six Ross 308 AP broilers, 47 days old, of both sexes, weighing about 3.51 kg, were slaughtered according to standard industrial practices, and evaluated for meat color, pH, chemical composition, collagen content, fatty acid profile, and histopathological parameters. Comparisons between normal and DCM-affected meat were performed using Student's t-test at the 5% significance level. Results: Histological analysis of muscle tissues affected by DCM showed myofiber degeneration, proliferation of inflammatory cells, fibroplasia, and necrosis with fibrosis. DCM samples had lower protein content and higher moisture, ash, insoluble collagen, total collagen, and pH. DCM-affected meat was redder and more yellowish. There were no differences in lipid or soluble collagen contents between groups. DCM-affected meat had higher percentages of arachidonic acid (C20:4n-6) and eicosapentaenoic acid (C20:5n-3). Conclusion: This study revealed that DCM-affected meat exhibits considerable changes in quality parameters.