• 제목/요약/키워드: trypsin activity

검색결과 404건 처리시간 0.034초

먹이섭취 후 흰다리새우, Litopenaeus vannamei (Boone) 소화기관의 trypsin 활성 및 배설률 (Post Feeding Trypsin Activity in the Digestive Organs and the Gastric Evacuation Rate of Litopenaeus vannamei (Boone))

  • 김수경;김대현;김봉래;김종식;조영록;서형철;김종화;한창희;장인권
    • 한국양식학회지
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    • 제19권1호
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    • pp.1-6
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    • 2006
  • 흰다리새우 양식기법의 최적화를 위하여 소화기간 동안의 간췌장, 전장 그리고 중장에서의 trypsin의 활성변화를 조사하였다. 체중에 대한 전장, 중장의 무게 그리고 그 무게 합의 비율은 섭취된 먹이의 이동 및 소화과정을 나타내는 지표로서 공급량과 잔류량에 의한 먹이섭취량을 측정하는 것 보다 더 정확한 지표로서 사용 가능하였다. 평균적으로 치대 먹이섭취량은 전장에서 먹이섭취 후 30분 이내에 체중에 0.3%로 나타났다. 또한 30분 이후부터 전장이 비워지기 시작되었으며 중장의 무게가 최대에 이르는 시각은 2시간째였다. $3{\sim}5$시간 후에는 먹이가 배설됨으로 인하여 중장의 체중에 대한 무게비가 감소하였으나 전장에서는 비교적 같은 비율을 유지하였다. 먹이섭취에 의한 trypsin활성변화는 간췌장에서 가장 커서 전장에서의 활성변화에 비하여 약 3배로 나타났다. 소화시간이 지날수록 간췌장에서의 trypsin 활성은 지속적으로 증가하였다. 전장에서의 trypsin 효소의 활성은 중장보다 약 $2{\sim}3$배정도 높았다 먹이섭취 후 2시간이 지났을 때 trypsin 활성은 303 n mol/mg/min였고, 4시간까지 이 활성이 유지($277{\sim}306$ n mol/mg/min)되었으며, 그 후에는 점차 감소하였다. 중장에서는 typsin 활성이 먹이를 섭취하여 한 시간이 지나면서 $65{\pm}29$ (SE) n mol/mg/min로 증가하였다. 그 이후에는 $80{\sim}97$ n mol/mg/min의 범위를 나타내었으며, 5시간이 경과하였을 때 $52{\pm}17$ (SE) n mol/mg/min로 감소하였고 소화관내에 잔류하고 있는 먹이 량은 최대 섭취량의 50%로 나타났다.

유우 Lactoferrin 효소가수분해물 항균 활성에 관한 연구 (Studies on the Antibacterial Activity of Enzymatic Hydrolyzates of Lactoferrin Derived from Bovine Colostrum)

  • 한수연;김종우
    • 농업과학연구
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    • 제25권1호
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    • pp.52-67
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    • 1998
  • 본 연구는 포유동물의 젖에 함유되어 있는 lactoferrin(LF)의 생리적 특성을 밝혀 기능성 식품 특히 항균작용을 이용한 식품제조업에의 이용을 위한 기초자료를 얻고자 실시하였다. 따라서 젖소의 초유로부터 lactoferrin을 분리 정제하여, 소화부위에 따른 lactoferrin의 항균활성을 분석하고자 pepsin, trypsin 및 chymotrypsin으로 분해하여 lactoferrin의 항균력을 측정하고, gel-filtration으로 분리 정제된 각각의 fraction별로 단백질을 정량하여 Escherichia coli와 Staphylococcus aureus에 접종하여 항균효과를 지니는 각 효소별 fraction의 분자량과 peptide fragment를 검토하였다. 1. 젖소의 초유로부터 분리 정제된 lactoferrin(LF)을 단백질 분해 효소인 pepsin, trypsin 및 chymotrypsin으로 분해한 결과 bovine lactoferrin은 SDS-PAGE를 수행하여 band를 확인할 수 있었다. pepsin으로 분해된 lactoferrin은 분자량 14KDa까지에서도 band를 확인할 수가 없었으며, trypsin과 chymotrypsin으로 분해한 lactoferrin은 분해되지 않은 lactoferrin이 존재함을 나타내고, 33KDa에서도 band를 확인할 수 있었다. 2. Sephadex G-50 column을 사용하여 bovine lactoferrin를 효과적으로 정제하였다. Sephadex G-50 column chromatography를 수행 한 결과 bovine lactoferrin은 Tris-HCl사이에서 용출되었으며, pepsin, trypsin 및 chymotrypsin으로 분해한 lactoferrin은 각각 2, 3, 2 개의 peak를 보였고, HPLC 분석결과 첫번째 peak는 주로 분해되지 않은 lactoferrin 수용체가 존재하는 것으로 확인되었으며, trypsin과 chymotrypsin처리에서 항균효과도 유사점을 관찰할 수 있었다. 3. 효소처리한 lactoferrin의 항균효과를 알아보기 위하여 Escherichia coli와 Staphylococcus aureus를 접종하여 항균활성을 비교하였다. 그 결과 각 효소에 대하여 pepsin으로 처리한 lactoferrin을 접종한 시험구가 대조구에 비하여 낮은 생장율을 보여 현저한 항균활성을 지님을 알 수 있었다. 그리고 trypsin과 chymotrysin에 의한 분해물도 미생물 배양 8시간까지는 효소 처리전 bovine lactoferrin보다는 항균활성을 나타냄을 알 수 있었다. 4. Sephadex G-50 column을 사용하여 분리 정제된 bovine lactoferrin fraction별로 SDS-PAGE를 실시한 결과 lactoferrin fraction의 경우는 chromatography 수행 결과와 비교하여, pepsin과 chymotrypsin 분해물은 저분자량임을 알 수 있었고, trypsin에 의한 lactoferrin만이 단일 band를 보임으로서 단백질 분해의 특징을 볼 수 있었다.

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Effect of Cultivars, Cooking and Processing on the Trypsin Inhibitor Activity of Soybean

  • Felipe, Penelope;Yang, Yoon-Hyung;Lee, Jung-Hee;Sok, Dai-Eun;Kim, Hyoung-Chin;Yoon, Won-Kee;Kim, Hwan-Mook;Kim, Mee-Ree
    • Preventive Nutrition and Food Science
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    • 제10권1호
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    • pp.6-10
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    • 2005
  • The trypsin inhibitor activity (TIA) of various soybean cultivars was evaluated by measuring the inhibition of trypsin activity using N-benzoyl-DL-arginine-p-nitro-anilide (BAPNA) as the substrate. The TIA values of eleven white shelled soybean cultivars including a glyphosate-tolerant soybean (16.58 to 17.90㎎/g) were not significantly different among cultivars. Black shelled soybeans had higher TIA values, ranging from 40.09 to 52.11㎎/g, compared to white shelled soybeans (p<0.05). When the TIA of commercially processed soybean foods were determined, no TIA was detected in soysauce, tofu and soybean paste. During conventional moist heating, the IT/sub 50/ (Time required to reach 50% inhibition of TIA) values were decreased as heating temperature and cooking pressure increased. The IT/sub 50/ values of moist heating were estimated to be 91.68, 37.71 and 19.50 min at 60, 80 and 100℃, respectively. The IT/sub 50/ value of microwave cooking was 4.75 min at medium heat, while that of the pressure cooking at 120℃ was only 2.62min. Moreover, there was a negative relationship between temperature and IT/sub 50/ values (R=0.92, p<0.01). The TIA of soybean sprouts was completely inactivated after heating at 100℃ for 5 min, although fresh soybean sprouts showed one fifth of the TIA value of white shelled soybeans. Based on our results, pressure cooking is the most effective cooking method to reduce TIA in soybeans.

Antioxidative and Neuroprotective Effects of Enzymatic Extracts from Leaves of Perilla frutescens var.japonica

  • Kim, Eun-Kyung;Lee, Seung-Jae;Lim, Beong-Ou;Jeon, You-Jin;Song, Min-Dong;Park, Tae-Kyu;Lee, Kwang-Ho;Kim, Bo-Kyung;Lee, Sang-Rak;Moon, Sang-Ho;Jeon, Byong-Tae;Park, Pyo-Jam
    • Food Science and Biotechnology
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    • 제17권2호
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    • pp.279-286
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    • 2008
  • The antioxidative activity of various enzymatic extracts from leaves of Perilla frutescens var. japonica was evaluated by measuring 1,1-diphenyl-2-picrylhydrazyl (DPPH), hydroxyl, and alkyl radical scavenging activity using an electron spin resonance (ESR) spectrometer. For this study, the leaves were enzymatically hydrolyzed by 8 carbohydrases (Dextrozyme, AMG, Promozyme, Maltogenase, Termamyl, Viscozyme, Celluclast, and BAN) and 9 proteases [Flavourzyme, Neutrase, Protamex, Alcalase, PP-trypsin (trypsin from porcine pancreas), papain, pepsin, $\alpha$-chymotrypsin, and BP-trypsin (trypsin from bovine pancreas)]. The DPPH radical scavenging activities of Promozyme and Alcalase extracts were the highest, and the $IC_{50}$ values were 77.25 and $109.66\;{\mu}g/mL$, respectively. All enzymatic extracts of the leaves scavenged hydroxyl radical, and the $IC_{50}$ values of Celluclast and pepsin extracts which were the highest activity were 243.34 and $241.86\;{\mu}g/mL$, respectively. The BAN and $\alpha$-chymotrypsin extracts showed the highest scavenging activities, and the $IC_{50}$ values were 21.13 and $33.23\;{\mu}g/mL$, respectively. The pepsin extracts from the leaves showed protective effect on $H_2O_2$-induced DNA damage. In addition, the pepsin extracts decreased cell death in PC-12 cells against $H_2O_2$-induced oxidative damage. The findings of the present study suggest that enzymatic extracts of the leaves possess antioxidative activity.

Effect of High Pressure on the Porcine Placenral Hydrolyzing Activity of Pepsin, Trypsin and Chymotrypsin

  • Chun, Ji-Yeon;Jo, Yeon-Ji;Min, Sang-Gi;Hong, Geun-Pyo
    • 한국축산식품학회지
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    • 제34권1호
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    • pp.14-19
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    • 2014
  • This study investigated the effects of protease treatments (trypsin, chymotrypsin, and pepsin) under various pressure levels (0.1-300 MPa) for the characteristics of porcine placenta hydrolysates. According to gel electrophoretic patterns, the trypsin showed the best placental hydrolyzing activity followed by chymotrypsin, regardless of the pressure levels. In particular, the peptide bands of tryptic-digested hydrolysate were not shown regardless of applied pressure levels. The peptide bands of hydrolysate treated chymotrypsin showed gradual decreases in molecular weights ($M_w$) with increasing pressure levels. However, the pepsin did not show any evidences of placental hydrolysis even though the pressure levels were increased to 300 MPa. The gel permeation chromatography (GPC) profiles showed that the trypsin and pepsin had better placental hydrolyzing activities under high pressure (particularly at 200 MPa), with lower $M_w$ distributions of the hydrolysates. Pepsin also tend to lower the $M_w$ of peptides, while the major bands of hydrolysates being treated at 300 MPa were observed at more than 7,000 Da. There were some differences in amino acid compositions of the hydrolysates, nevertheless, the peptides were mainly composed of glycine (Gly), alanine (Ala), hydroxyproline (Hyp) and proline (Pro). Consequently, the results indicate that high pressure could enhance the placental hydrolyzing activities of the selected proteases and the optimum pressure levels at which the maximum protease activity is around 200 MPa.

Overexpression of sprA and sprB Genes is Tightly Regulated in Streptomyces griseus

  • KIM , YOON-HEE;CHOI, SI-SUN;KANG, DAE-KYUNG;KANG, SANG-SOON;JEONG, BYEONG-CHUL;HONG, SOON-KWANG
    • Journal of Microbiology and Biotechnology
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    • 제14권6호
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    • pp.1350-1355
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    • 2004
  • The sprA and sprB genes, encoding the chymotrypsin-like proteases Streptomyces griseus protease A (SGPA) and Streptomyces griseus protease B (SGPB), and the sprT gene that encodes Streptomyces griseus trypsin (SGT) were cloned from S. griseus and were overexpressed in various strains of S. griseus. When the sprT gene was introduced into S. griseus, trypsin activity increased 2-fold in the A-factor deficient mutant strain, S. griseus HH1, and increased 4-fold in the wild strain, S. grise us IFO 13350. However, there was no detectable increase of chymotrypsin activity in the transformants of S. griseus with either sprA or sprB, in contrast to the results obtained from S. lividans as a heterologous host. To solve the negative gene dosage effects in S. griseus, either the sprA or the sprB genes with their own ribosome binding sites were linked to the downstream of the entire sprT gene, and the coexpression efficiency was examined in S. lividans and S. griseus. The transformants of S. lividans with either pWHM3-TA (sprT+sprA) or pWHM3­TB (sprT+sprB) showed 3-fold increase of trypsin activity over that of the control, however, only the transformant of pWHM3-TB demonstrated 7-fold increase in chymotrypsin activity, indicating that the pWHM3-TB has a successful construction for the overexpression of chymotrypsin in Streptomyces. When the coexpression vectors were introduced into S. griseus IFO 13350, the trypsin level sharply increased by more than 4-fold, however, the chymotrypsin level did not increase. These results strongly suggest that the overexpression of the sprA and sprB genes is tightly regulated in S. griseus.

대두발아(大豆發芽)에 따른 Trypsin Inhibitor Activity와 Protein Pattern의 변화(變化) (The Trypsin Inhibitor Activity and Protein Pattern of the Soybean During Germination)

  • 손혜숙;박정륭;이성우
    • Applied Biological Chemistry
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    • 제20권2호
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    • pp.182-187
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    • 1977
  • 본 실험은 대두(大豆)의 발아(發芽)에 따른 trypsin inhibitor activity(TIA)와 protein pattern의 변화에 관하여 조사함과 아울러 그 상관관계를 살퍼보기위한 목적으로 시도되었다. 자엽의 TIA는 발아(發芽)과정중(中) 조금 감소하였고, 배축에서는 급격히 감소해서 발아(發芽) 제 7일에는 제2일의 50%이하로 줄었다. 그리고 발아(發芽) 제 2,3,4일의 defatted dry sample에서 배축은 자엽보다 더 높은 TUI를 보여줬으며 배축의 수분함량이 자엽에 비해 높으므로 fresh sample당(當) TIA는 자엽보다 더 낮았다. 그리고 protein pattern은 자엽과 배축에 있어서 분자량이 큰 15S등의 polymer (band 1), 11S (band 2) 그리고 7S (band 3)가 감소했고 Rm치(値) 자엽의 band 5를 비롯하여 $0.5{\sim}1.0$사이에 높은 mobility를 가진 물질들이 생성(生成)되었다. 자엽의 band 4와 배축의 band 6은 거의 변하지 않았다. 그리고 발아에 따라 TIA의 감소와 저 장단백질의 감소는 있었으나 그 감소량이 서로 일치하지는 않았다.

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Relationship between White Spot Symptom and Physiological Status of Two Penaeid Shrimps

  • Kim, Su Kyoung;Kim, Myung Seok;Park, Myoung Ae;Kim, Su mi;Jang, In Kwon;Kim, Seok Ryel;Cho, Miyoung
    • 환경생물
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    • 제35권4호
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    • pp.461-467
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    • 2017
  • Shrimps infected with WSSV(White Spot Syndrome Virus) generally exhibit white spots in their inner space of carapaces as an acute clinical sign. In an effort to identify the correlation between this acute clinical sign and the condition, the index factors (RNA/DNA concentration and ratio, trypsin activity) were analyzed. A total 580 farmed Fenneropenaeus chinensis and 130 Lithopenaeus vannamei were collected from western and southern fifteen outdoor ponds in Korea. The status of the white spot pathology was divided into four stages (stage 0, stage I, stage II, and stage III), in accordance with the clinical signs as to the size and area of white spots. A significant decrease in RNA concentration and RNA/DNA ratio for multi-infected fleshy prawn (WSSV and vibrio sp.) occurred during the stage III (the whole carapace is covered with a white spot). In particular, RNA/DNA ratio was significantly lower as $1.47{\pm}0.04$ than other groups. A similar trend was also found in the single infection (WSSV), but the decrease was less than the multi-infection. In the species comparison, both species were vulnerable to the multi-infection, but L. vannamei was more sensitive than F. chinensis(ANOVA, p<0.05): A significant decrease in RNA concentration and RNA/DNA ratio was first found in stage II for the former species, while it was found in stage III for the latter species. Trypsin activity was also showed a similar tendency with nucleic acid variation. Multi-infected shrimp showed drastically decrease of trypsin activity. According to the results, clinical signs of the white spot under carapace have an only physiological effect on shrimp if they covered entirely with white spots.

트립신 처리에 따른 적송잎 추출물의 항산화 활성 및 항균 효과 (Antioxidant and Antimicrobial Activities of Trypsin-treated Pinus densiflora Ethanol Extract)

  • 문기은;박교현;이범주;김배환
    • 한국환경보건학회지
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    • 제44권3호
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    • pp.293-300
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    • 2018
  • Objectives: We investigated the antioxidant and antibacterial activities of Pinus densiflora ethanol extracts (PDEE) treated with trypsine as a protease. Methods: Various antioxidant activities were evaluated by measuring total contents of polyphenol and flavonoid, DPPH electron-donating ability and $ABTS^+$ radical scavenging activity of test material. To compare the antibacterial activity, paper disc diffusion assay was performed against two resident bacteria in human skin (Staphylococcus aureus and Staphylococcus epidermidis). Results: As for the total contents of polyphenol and flavonoid, and the electron-donating ability and ABTS+ radical scavenging activity, both PDEE and trypsin-treated Pinus densiflora ethanol extract (T-PDEE) showed high antioxidant activity in dose-dependent manner. And the T-PDEE showed slightly higher activity than PDEE, which indicated protease treatment seemed to affect in antioxidant activity. In the result of paper disc diffusion assay, antibacterial activity was confirmed in all two types of skin resident bacteria. T-PDEE was more active than PDEE and it seems that treatment of protease may increase the antibacterial activity of PDEE. Conclusion: All of these results, we confirmed that treatment of protease to PDEE can increase the antioxidant and antibacterial activities, and it can be explained thought that this would be applicable as a cosmeceutical material in the future.

생쥐 배아의 부화에 관여하는 Trypsin 유사 효소의 발현과 역할 (Expression and Role of Trypsin-Like Enzyme Involved in Hatching of Preimplantation Mouse Embryos)

  • 김수경;강희규;전진현;최규완;김문규
    • 한국발생생물학회지:발생과생식
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    • 제5권1호
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    • pp.17-21
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    • 2001
  • 생쥐 초기배아의 체외배양 시 부화에 관련된 단백질 분해효소의 발현 시기와 존재부위를 알아보고 trypsin억제제 benzamidine을 배양액에 첨가하여 부화효소의 역할을 살펴보았다. 부화 효소로 제안되고 있는 trypsin 유사효소의 발현부위를 확인하기 위해 rhodamine이 부착되어 있는 Trypsin subsfrate probe를 이용하여 형광염색하였다. 생쥐 배아의 발생과정에서 trypsin 유사효소의 발현은 후기 상실 배아에서부터 관찰되었으며, 포배기 배아에서는 영양배엽 표면에서 전체적으로 관찰되었다. 특히, 부화가 진행되고 있는 배아의 부화 개시 부위 (blebbing)에서 그 염색 정도가 상대적으로 강함을 확인할 수 있었다. 생쥐 4-세포기 배아의 체외배양 시 배양액에 trypsin 억제제인 benzamidine을 ImM 농도로 첨가하였을 때 포배기로의 발생률은 영향을 받지 않았지만, 부화율은 15.8%로 대조군의 83.0%에 비해 유의하게 (p<0.02) 낮게 나타났다. 배아의 발생단계에 따라 5mM의 benzamidine을 12시간 동안 처리한 경우 부화율이 8.7%로 대조군의 83.0%에 비해 유의하게(p<0.01)낮았다. 결론적으로, trypsin 유사효소는 초기 포배기에서부터 발현되기 시작하며 특히, 후기 포배기에서 그 효소의 작용이 부화 과정에 커다란 영향을 미치는 것이 확인되었다. 또한 배양중 부화 과정에서는 배아 자체에서 분비되는 trypsin 유사효소의 역할만으로도 부화할 수는 있지만 생체 내에서는 배아와 자궁내막 상피와의 상승적 상호 작용에 의해 부화과정이 더 활발히 진행되는 것으로 생각된다.

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