• 한국식품영양학회지
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• 제8권4호
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• pp.335-343
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• 1995

In order to enhance the utility of alaska-pollack, the optimum conditions for the preparation of pronase hydrolysate. The optimum temperature and pH for the hydrolysis of alaska-pollack by pronase were 4$0^{\circ}C$ and pH 7.0. The reaction time and enzyme concentration were 4 hr and 1,000 units per g of substrate. Under the above optimum conditions alaska-pollack was hydrolysed by pronase yielding a hydrolytic degree of about 89eye. The bitterness and hyrophobicity of pronase hydrolysate were decreased with increasing reaction time. Hydrophobic amino acids(Tyr, Met, Ala, flu, Leu, and Phe) were increased for 2 hr, but fur thor hydrolysis was showed decrease of hydrophobic amino acids content. Palatable amino acids (Asp, Glu, Pro, Ser, Thr and Gly) were increased with hydrolysis time.

• Applied Biological Chemistry
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• 제35권5호
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• pp.339-345
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• 1992

명태육의 식품가공적성과 이용성을 높이기 위해 pronase에 의한 명태단백의 가수분해조건과 fruit-와 stem-bromelain에 의한 plastein의 합성 반응조건을 검토하였다. Pronase 가수분해 최적조건인 반응pH 7.0, 반응온도 $40^{\circ}C$, 기질 g당 효소첨가량 1,000units 및 반응시간 4시간에서 89% 분해도를 보이는 명태단백의 가수분해물을 제조하였다. Plastein은 pH가 각각 5.0(stem-bromelain)과 7.0(fruit-bromelain)으로 조정된 기질 30% 용액에 bromelain 1%를 가하여 $40^{\circ}C$, 24시간 진탕반응하여 합성하였다. 이 최적조건에서 합성된 plastein은 각각 22.6과 20.8 아미노산 잔기를 가진 펩타이드로 구성되어 있었으며 관능검사에 의해 반응초보다 크게 쓴맛이 제거되는 결과를 나타내었다.

• 한국수산과학회지
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• 제49권5호
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• pp.594-599
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• 2016

Infection with HIV (Human immunodeficiency virus), over time, develops into acquired immunodeficiency syndrome (AIDS). The development of non-toxic and effective anti-HIV drugs is one of the most promising strategies for the treatment of AIDS. In this study, we investigated the anti-HIV-1 activity of gelatin hydrolysates from Alaska pollack skin. Gelatin hydrolysates were prepared using four enzymes (alcalase, flavourzyme, neutrase, and pronase E). Among these, the pronase E gelatin hydrolysate was found to inhibit HIV-1 infection in the human T cell-line MT4. It exhibited inhibitory activity on HIV-1_IIIB-induced cell lysis, reverse transcriptase activity, and viral p24 production at noncytotoxic concentrations. Moreover, it decreased the activation of matrix metalloproteinase-2 (MMP-2) in vitro. Because HIV infection-induced activation of MMP-2 can accelerate collagen resolution and collapse of the immune system, pronase E gelatin hydrolysate might prevent the activation of MMP-2 in cells, resulting in collagen stabilization and immune cell homeostasis consistent with anti-HIV activation. These results suggest that pronase E gelatin hydrolysate could potentially be incorporated into a novel therapeutic agent for HIV/AIDS patients.

• KSBB Journal
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• 제6권4호
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• pp.327-336
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• 1991

수산물 가공시 부산물로 얻어지는 어피(魚皮)를 보다 효율적으로 이용하기 위하여 효소로 대구피를 가수분해할 때 가수분해조건을 구명하였으며 그 가수분해물을 이용한 천연조미료(모조간장 및 복합조미료)의 개발을 시도하였다. pH-drop법으로 대구피분해에 있어서의 collagenase, trypsin 및 pronase의 활성을 비교해 본 결과 pronase가 가장 활성이 높았으며 이 pronase의 $K_m$ 및 $V_{max}$값은 각각 1.82 mgN/ml, 0.06 mgN/mL/min였다. Pronase에 의한 대구피 가수분해조건은 반응온도 $50^{\circ}C$, 반응시간 3시간, pH6, 효소농도 0.03%였으며, 이 조건하에서의 가수분해도는 78.8%였다. 그러나 대구피를 collagenase로 1시간 분해시킨 후 pronase로 처리할 경우 가수분해도는 90.83%였다. 이때 가수분해물의 분자량은 8,000 dalton이었다. 아미노산 조성은 glycine(27.95%), glutamic acid(10.94%), proline(10.48%), aspartic acid(7.47%), serine(7.39%)이 전체 아미노산의 64.23%였으나 쓴맛을 내는 valine, methionine, isoleucine, leucine, phenylalanine, histidine 등은 13.05%에 불과하였다. 가수분해물과 기타 부원료로 제조한 모조간장원액과 시판 100% 양조간장을 8:2(v/v)로 혼합한 모조간장은 시판대두간장에 비해 최소유의차 검정 결과 맛, 색 및 종합평가면에서 5% 유의수준내에서 유의차가 없었다. 가수분해물 31.7% 함유한 복합조미료도 시판 복합조미료와 관능적으로 비교해 본 결과 복합조미료로서의 손색이 없는 제품이었다.

• Fisheries and Aquatic Sciences
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• 제12권3호
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• pp.163-170
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• 2009

This study was conducted to obtain the gelatin fraction with a high anti oxidative activity from Alaska pollock surimi by-products using a two-step enzymatic hydrolysis and ultrafiltration. Among gelatin hydrolysates from refiner discharge of Alaska Pollock surimi, the highest antioxidative activity (81.5%) resulted from gelatin hydrolysate sequentially treated with Pronase E and Flavourzyme each for 2 hr. However, no difference was seen in the anti oxidative activity of the second hydrolysate (Pronase E-/Flavourzyme-treated hydrolysate) when compared to the permeate fractionated through a 10-kDa membrane. The results suggest that the Pronase E-/Flavourzyme-treated hydrolysate from refiner discharge gelatin of Alaska pollock surimi can be used as a supplementary raw material for improving health functionality.

• 한국식품과학회지
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• 제28권4호
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• pp.678-683
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• 1996

Pronase 등 8개의 단백분해효소를 사용하여 말쥐치를 가수분해시 생성되는 펩타이드의 양을 측정한 결과, bromelain과 neutrase에 의한 가수분해물의 펩타이드 생성량은 4시간 가수분해시 6.13 mg/ml와 6.01 mg/ml로 높은 생성량을 보였으며, 유리아미노산의 생성량은 4시간 가수분해시 alcalase에 의한 가수분해물이 4.20 mg/ml로 높은 유리 아미노산의 생성량을 보였다. 가수분해도를 측정한 결과, 4시간 가수분해시 esp/sav와 alcalase의 가수분해물은 88.9%와 86.2%의 비교적 높은 가수분해도를 보였다. 또한 핵산관련 물질은 5'-GMP가 다른 핵산 관련물질에 비해 높은 생성량을 보였다. 가수분해물의 펩타이드의 평균길이는 $8.5{\sim}14.5$로 bromelain에 의한 가수분해물이 가장 짧은 펩타이드 길이를 가진 반면, neutrase에 의한 가수분해물은 14.5로 가장 긴 펩타이드로 구성되었다.

• Bulletin of the Korean Chemical Society
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• 제20권11호
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• pp.1299-1302
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• 1999

Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) was used to demonstrate cross-linking of peptides induced by transglutaminase. The presence of ε-( Υ-glutamyl)lysine isopeptide cross-link in the acid hydrolysate of the cross-linking reaction mixture was also demonstrated by MALDI-TOF-MS without prior separation. MALDI-TOF-MS quickly provided peptide mass maps after pronase digestion of the cross-linked peptide adduct, which enabled us to monitor the hydrolytic sequence. Pronase appears to preferentially hydrolyze peptide bonds distant from the cross-link before hydrolyzing peptide bonds around the cross-link. The results suggest that pronase digestion followed by MALDI-TOF-MS could be used for determination of amino acid sequence around a modification site.

• KSBB Journal
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• 제15권6호
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• pp.635-643
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• 2000

To compare the antioxidative activities of fish skin and bovine skin gelatin hydrolysate, gelatin hydrolysates from Alaska pollack and bovine skin were prepared by various enzymatic hydrolysis methods (1st step, Alcalase; 2nd step, pronase E; 3rd step, collagenase) using a continuous three-step membrane reactor. The molecular weight distributions of the 1st, 2nd and 3rd step hydrolysates were 7∼10 kDa, 2∼5 kDa and 0.7∼0.9 kDa, respectively. The antioxidative activity of fish skin gelatin hydrolysate was stronger than that of bovine skin gelatin hydrolysate, and in particular, both of 2nd step hydrolysates showed more antioxidative activity than hydrolysates of any other step. The optimum antioxidative activity concentration of the 2nd step hydeolysates of fish and boving skin were 1% (w/w) in a linoleic acid water-alcohol emulsion. In cultured cells exposed to t-butyl hydroperoxide (t-BHP), the 2nd step hydrolysate of fish skin gelatin delayed cell death most. These results suggest that the antioxidative activity of fish skin gelatin hydrolysate is higher than that of bovine skin gelatin hydrolysate because of their different amino acid contents.

• BMB Reports
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• 제34권3호
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• pp.219-224
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• 2001

To identify the antioxidative peptides in the gelatin hydrolysate of bovine skin, the gelatin was hydrolyzed with serial digestions in the order of Alcalase, pronase E, and collagenase using a three-step recycling membrane reactor. The second enzymatic hydrolysate (hydrolyzed with pronase E) was composed of peptides ranging from 1.5 to 4.5 kDa, and showed the highest antioxidative activity, as determined by the thiobarbituric acid method. Three different peptides were purified from the second hydrolysate using consecutive chromatographic methods. This included gel filtration on a Sephadex G-25 column, ion-exchange chromatography on a SP-Sephadex C-25 column, and high-performance liquid chromatography on an octadecylsilane chloride column. The isolated peptides were composed of 9 or 10 amino acid residues. They are: Gly-Glu-Hyp-Gly-Pro-Hyp-Gly-Ala-Hyp (PI), Gly-ProHyp-Gly-Pro-Hyp-Gly-Pro-Hyp-Gly (PII), and Gly-ProHyp-Gly-Pro-Hyp-Gly-Pro-Hyp (PIII), as characterized by Edman degradation and fast-atom bombardment mass spectrometry. The antioxidative activities of the purified peptides were measured using the thiobarbituric acid method, and the cell viability with a methylthiazol tetrazolium assay The results showed that PII had potent antioxidative activity on peroxidation of linoleic acid. Moreover, the cell viability of cultured liver cells was significantly enhanced by the addition of the peptide. These results suggest that the purified peptide, PII, from the gelatin hydrolysate of bovine skin is a natural antioxidant, which has potent antioxidative activity.

• 한국식품영양과학회지
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• 제21권5호
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• pp.519-524
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• 1992

탈지유채박(Brassica napus var. Youngsan)으로부터 추출, 정제하여 얻어진 유채단백질을 가수분해하여 가수분해물의 이화학적 및 기능적 특성을 조사하였다. 가수분해물의 UN 및 고유형광 스펙트럼은 각각 274nm, 360nm에서 최대치를 나타내었다. 황색도는 약간 감소한 반면 표면 소수성은 약 4배 감소하였다. SDS-PAGE 분석 결과 상당부분이 1.4~$1.2{\times}10^4$ dalton의 분자량을 가진 band로 나타났으며, pH별 용해도는 산성부근에서 10~15% 정도 증가하였고, 수분 및 유흡수성, 거품 팽창성, 에멀젼 안정성은 증가한 반면 절대 점도, 열 및 칼슘 응고성, 거품 안정성, 에멀젼 활성지수는 감소하였다.