• 제목/요약/키워드: A-esterase

검색결과 336건 처리시간 0.031초

염장과정 중 무의 조직감과 이와 관련된 화학적, 효소활성 변화 (Changes in Textural Properties of Korean Radish and relevant Chemical, Enzymatic Activities during Salting)

  • 이희섭;이귀주
    • 한국식생활문화학회지
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    • 제8권3호
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    • pp.267-274
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    • 1993
  • 무의 염장과정 중 소금의 침투량, 담금액의 pH와 산도 및 조직감의 변화와 이와 관련된 화학적 변화, 효소활성 변화를 알아보고자 하였다. 그 결과는 다음과 같다. 1. 3%와 10% 소금용액에서 생무와 열처리한 무를 담구어 4일간 저장하였을 때, 무 조직 내의 소금농도는 2일까지는 빠르게 증가하였으며 침투속도는 10% 소금용액에서 더욱 컸으며 열처리구에서 더 높았다. 2. 무의 염장과정 중 담금액의 pH는 낮아지고 산도는 증가하여 염장 10일째에 pH는 3.45, 산도는 0.52%를 나타내었다. 3. 힘-거리곡선의 형태는 생무의 경우, 파열점(a)과 최대 압착변형점(c)이 일치하거나 a 이후에 더 큰 c가 나타나서 positive slope을 갖는 곡선이 주종을 이루나, 염장한 무는 a와 c가 일치하면서 특징적인 하나의 peak만을 나타내거나 혹은 a 이후에 최대변형력이 작아지면서 negative slope의 곡선이 주로 나타났다. 또한, 염장이 진행됨에 따라 무의 peak 수는 점차 줄어들었다. 압착시험, 침투관통시험 및 절단시험을 통하여 무의 조직감 변화를 측정한 결과, 무의 압착변형력은 염장과정 중 전반적으로 감소하였다. 크기가 다른 탐침을 이용하여 침투관통시험을 행한 결과, 전반적으로 침투관통력은 감소하였으며 탐침의 직경이 클수록 침투관통력은 증가하는 것으로 나타났다. 또한 절단력은 염장과정 중 증가하였다. 이로부터 염장과정 중 무의 견고성은 감소하였으며 무의 질긴정도(toughness)는 증가하는 것으로 생각된다. 4. AIS로부터 펙틴질을 분획하여 그 함량을 측정한 결과, 염장과정 중 HWSP 함량과 HXSP 함량은 증가하였으며 HClSP 함량은 감소하였다. 5. 염장과정 중 효소 활성의 변화는 발효 4일째까지 증가하다가 감소하였으며 무 염장액에서보다 무 고형분에서의 PG 활성이 크게 나타났다. PE 활성은 염장과정 중 무 고형분과 무 염장액에서 계속 감소하였다. 한편, Cx-cellulase은 염장 초기에는 거의 활성을 나타내지 않았으나 염장 2일째부터 활성이 나타나기 시작하였다.

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TMT 유도성 인지 기능 상실에 대한 대보(밤 품종) 내피 추출물의 효과 (Effect of Daebo (Castanea crenata) Inner Skin Extract on TMT-induced Learning and Memory Injury)

  • 김현주;정지희;조유나;진동은;진수일;김만조;허호진
    • 한국식품과학회지
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    • 제45권5호
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    • pp.661-665
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    • 2013
  • 본 연구에서는 국내 대표 밤 품종인 대보(Daebo)의 내피를 활용하여 TMT 유도성 인지 기능 상실에 대한 개선 효과를 연구하였다. 실험에서 각 농도별(5, 10, 20 mg/kg of body weight)로 대보 내피 에틸아세테이트 분획물을 섭취한 mouse를 TMT로 인지기능 손상을 유발하여 Y-maze test와 passive avoidance test한 결과, Y-maze test에서 분획물을 섭취한 group이 TMT 단독 처리군과 비교하였을 때 공간 인지기능을 개선시켰고, passive avoidance test 또한 latency time이 증가한 것으로 나타나 TMT에 의해 유발되는 뇌 신경독성 동물 모델로부터 기억 및 학습능력 개선 효과를 갖는 것으로 확인되었다. 또한 in vivo 동물 실험 후 mouse로부터 적출된 whole brain tissue를 대상으로 ex vivo AChE 활성 및 MDA 함량측정 실험한 결과, 에틸아세테이트 분획물이 TMT효과 대비 AChE의 활성을 일부 유의적으로 억제하는 것을 알 수 있었다. 결론적으로 대보 내피 에틸아세테이트 분획물은 신경전달물질인 AChE의 활성을 저해하고 뇌 신경세포 보호 효과를 통하여 인지기능 개선 효과를 유도할 수 있는 것으로 사료된다.

Dichlorvos가 흰쥐 심근의 미세구조에 미치는 영향 (A Study on the Ultrastructural Changes of Cardiac Muscle in Dichlorvos Treated Albino Rat)

  • 백태경;이화모;정호삼
    • Applied Microscopy
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    • 제24권3호
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    • pp.23-33
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    • 1994
  • It is well known that dichlorvos (DDVP), an organophosphate insecticide in common use, is so easily and rapidly hydrolyzed and excreted that it has usually little toxic effect on human body. In these days, however, it is widely used as an industrial and domestic insecticide and as an anthelmintic agent for animals, so that the accident of chemical poisoning occurs frequently. DDVP acts as a powerful inhibitor of carboxylic esterase, which can cause accumulation of acetylcholine at the synapses so paralysis of muscle and the transmission failure in cholinergic synapses dueing to desensitization of acetylcholin receptor may occure. Moreover accumulation of the acetylcholine brings about the elevation of the cyclic-AMP, which alters the cellular metabolisms of nucleic acid, carbohydrate, protein and lipid. Present study has undertaken to investigate the cardiotoxic effect of DDVP by electron microscopic study. A total of 30 Sprague-Dawley strain rats, weighing about 250gm were used as experimental animals. 2mg/kg/day of DDVP is intraperitonealy injected 3 times with intervals of every other day. On 1 day, 3 days, 5 days, 7 days and 14 days after drug administration, the animals were sacrified by cervical dislocation. Left ventricular cardiac muscles were resected and sliced into $1mm^3$. The specimens were embedded with Epon 812 and prepared by routine methods for electron microscopical observation. All preparations were stained with lead citrate and uranyl acetate and then observed with Hitachi-600 transmission electron microscope. The results were as follows: 1. In the cardiac muscle of DDVP treated rats, mitochondria with disorganized double membrane and mitochondrial crista, and vacuole formation in mitochondrial matrix were observed. But structures of mitochondria were recovered to normal in 14 days group. 2. In the cardiac muscle of DDVP treated rats, cisternae of sarcoplasmic reticulum were dilated and sacculated. But these changes were recovered to normal in 14 days group. 3. In the cardiac muscle of DDVP treated rats, glycogen particles around damaged myofibrils were decreased. But amount of glycogen particles were restored in 14 days group. 4. In the cardiac muscle of DDVP treated rats, disruption and discontinuation of myofilaments and disorganization of Z-disc were observed. But the structures of myofibrils were recovered to normal in 14 days group. It is consequently suggested that DDVP would induce the reversible degenerative changes on the ultrastructures in cardiac muscle of rat.

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추출방법에 따른 참취(Aster scaber Thunb.)의 페놀화합물 함량과 생리활성 및 소화효소 저해 효과 (Polyphenolic Compounds, Physiological Activities, and Digestive Enzyme Inhibitory Effect of Aster scaber Thunb. Extracts According to Different Extraction Processes)

  • 김재원;윤광섭
    • 한국식품영양과학회지
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    • 제43권11호
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    • pp.1701-1708
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    • 2014
  • 참취의 활용 및 생리활성을 증가시킬 수 있는 적정 추출방법을 알아보고자 상온교반, 환류냉각, 가압가열, 저온고압 및 초음파 추출법을 이용하여 추출한 두벌 째 수확 참취 추출물의 생리활성을 비교하였다. 추출 수율은 환류냉각추출, 초음파추출, 가압가열추출, 상온추출, 저온고압추출 순으로 높았다. 폴리페놀, 플라보노이드 함량은 저온고압추출에서 유의적으로 높았고, 상압가열, 고온고압, 초음파추출에서는 대등한 함량을 나타내었다. 페놀화합물 정량의 경우 chlorogenic acid 함량은 가압가열추출에서 유의적으로 높았으며 cynarin 함량의 경우 환류냉각, 저온고압 및 초음파 추출에서 유의적으로 높았고, astragalin 함량의 경우 저온고압추출에서 높은 함량이 검출되었다. Xanthine oxidase(XO), angiotensin I-converting enzyme(ACE), HMG-CoA reductase 저해활성의 경우 저온고압추출 및 초음파 추출물에서 우수한 활성을 나타내었으며, 소화효소 저해활성(${\alpha}$-amylase, trypsin, lipase)에서도 유사한 경향을 나타내었다. 이러한 결과를 종합해 볼 때 저온고압 및 초음파 추출물에서 소재 활용가치가 높을 것으로 사료되며 천연 항산화제 및 기능성 증진을 위한 소재로 이용 가능할 것으로 판단된다.

Effects of Common Bile Duct Ligation on Serum and Hepatic Carboxylesterase Activity in Ethanol-Intoxicated Rats

  • Ahn, Kwan-Wook;Kim, You-Hee
    • BMB Reports
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    • 제32권4호
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    • pp.331-338
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    • 1999
  • Ethanol catabolism is thought to produce metabolic disorders resulting in alcoholic liver disease. To investigate the mutual effects of ethanol catabolism and cholestasis induced by common bile duct ligation on the activities of carboxylesterase, we have determined the enzyme activities in rat hepatic (cytosolic, mitochondrial, and microsomal) preparations as well as in rat serum using ten animal models: normal rats (group 1), sham-operated rats (group 2), common bile duct-ligated rats (group 3), ethanol-intoxicated rats (group 4), sham-operation plus chronic ethanol-intoxicated rats (group 5), common bile duct-ligated plus chronic ethanol-intoxicated rats at 1.5h and 24h (groups 7A and 7B), and duct-ligated and acute ethanol intoxicated rats at 1.5 h and 24 h (groups 8A and 8B). The $K_m$ and $V_{max}$ values of carboxylesterase from these hepatic preparations of cholestatic rat liver combined with chronic ethanol intoxication were also measured by using ethyl valerate as the substrate from the 14th day post-ligation. Carboxylesterase activities of all hepatic preparations and rat serum (group 3) showed significant decreases compared to the activities from the sham-operated control (group 2). Enzyme kinetic parameters indicated that $V_{max}$ of carboxylesterase from all the hepatic preparations in cholestatic rats (group 3) decreased significantly, although the $K_m$ values were about the same as in the sham-operated control (group 2). When cholestasis was combined with chronic ethanol intoxication (group 6), carboxylesterase activities showed further decrease in all the hepatic preparations and serum compared to the control activity (group 5). The $V_{max}$ also decreased significantly, although $K_m$ values did not change. When common bile duct ligation was combined with acute ethanol intoxication (group 8), the enzyme activities in the rat liver and serum showed significant decrease compared to the activity from acute ethanol-intoxicated rats (group 7). However, quite contrary to this, the activities of serum from acute ethanol intoxication 1.5 h (group 7A) increased significantly compared to the activities in the normal control (group 1). These results, therefore, suggest that the biosynthesis of hepatic carboxyl-esterase seems to decrease when cholestasis is combined with chronic and acute ethanol intoxication, and the decrease in activity is more significant than from cholestasis alone.

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국내 생막걸리에서 분리한 야생 효모의 특성 (Characteristics of wild yeast isolated from non-sterilized Makgeolli in Korea)

  • 정수지;여수환;문지영;최한석;백성열
    • 한국식품저장유통학회지
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    • 제24권7호
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    • pp.1043-1051
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    • 2017
  • 본 연구는 각 지역의 생막걸리에서 분리된 야생 효모의 다앙한 발효학적 특성을 조사하기 위해 34종을 수집하고 효모를 분리, 동정하였다. 야생효모는 62 균주로 분리되었고, 26S rDNA 염기서열을 분석한 결과, Saccharomyces cerevisiae와 Pichia kudriavzevii로 동정 되었다. 62개의 균주들 중 발효학적 특성이 우수한 균주들을 선발하기 위해 황화수소와 $CO_2$ 생성능, 알코올 내성, 응집성 및 향기 성분 생성능을 분석하였다. 알코올 내성과 $CO_2$ 생성능의 상관성을 확인하기 위해 주성분분석(Principal Components Analysis)을 하였다. PC1 양의 방향에 강하게 부하되는 균주는 YM37, YM31, YM32, YM22로 분석되었으며, 총 0.14-0.18 g/72 h의 $CO_2$ 생성으로 대조군에 비해 높은 발효능을 보였고, 이들 중 YM22를 제외하고 불쾌취인 황화수소를 생성하지 않았다. 또한 이 4개의 균주들은 알코올 내성 15% 이상을 보유하며, 응집성은 0.5-1.0 mL 사이인 flocculation type으로 확인되었다. API 분석 및 cerulenin, TFL 저항성을 실험한 결과, 향기성분 생성능이 좋은 효모는 황화수소와 알코올 내성, 응집성 실험에서 우수한 발효학적 특성을 보인 YM37, YM31, YM32, YM22를 포함한 총 33개로 확인되었다. 이러한 결과를 통해 우리나라 생막걸리에서 분리한 야생 효모의 알코올 발효 및 향미 특성을 확인하였으며, 분리된 야생 효모는 주류 제조의 종균 효모로 이용 가능성을 확인하였다.

Multistix$^{(R)}$-SG와 Comgur-9-test$^{(R)}$RL에 의한 요시험지봉검사 성적의 비교 (Comparison of the Results of Multistix$^{(R)}$SG and Comber-9-Test$^{(R)}$ RL Urine Dipstick Assay)

  • 김대철;김경동;정보찬;김정숙;조길호
    • Journal of Yeungnam Medical Science
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    • 제8권1호
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    • pp.42-52
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    • 1991
  • 최근 널리 사용되고 있는 제조회사가 다른 두가지 요시험지봉(Combur-9-test$^{(R)}$ RL & Multistix$^{(R)}$-SG)으로 요검사를 실시하면, 그 결과치의 표현에 있어 차이가 있으므로, 결과치 판정시 질병의 진단이나 치료의 효과 판정 및 경과관찰에 있어서 발생할 수 있는 혼란을 줄이고자, 환자검체와 표준검체에서 실시한 요시험지봉 검사결과를 비교 검토하여 아래와 같은 결론을 얻었다. 또한 두 시험지봉검사에 결과를 교환함에 있어 상응하는 결과치도 조사하였다. Combur-9-test RL 및 Multistix-SG를 이용하여, 1990년 12월 16일 부터 15일간 영남대학교 의과대학 부속병원 임상병리과에 요검사가 의뢰된 501명의 환자검체를 대상으로 하여 요시험지봉으로 화학적검사를 반정량적으로 시행한 결과 대체로 ${\pm}1$등급 범위내에서 일치하였다. Combur-9-test RL을 이용한 leukocyte esterase 검사와 요침사검사간의 비교에서 현미경적 농뇨와의 일치율은 83.7%, 민감도 48.1%, 특이도 90.3%, 양성예측율 47.4% 및 음성예측율 90.5%로 나타났다. Combur-9-test RL을 사용한 nitrite검사와 요배양검사간의 비교에서 요배양 양성과의 일치율은 93.0%, 민감도 19.4%, 특이도 84.7%, 양성예측율 53.8% 및 음성예측율 94.1%로 나타났다. 단백의 주 성분이 알부민 및 글로부린인 검체에서 실시한 요단백검사에서는 양자 모두에서 sulfosalicylic acid 법이 가장 민감하였고, 다음은 Multistix-SG, Combur-9-test RL의 순이었다. 요빌리루빈 및 요당검사에서는 두시험지봉이 비슷한 민감도를 나타내었다. 요중 백혈구검사에서는 요침사검사가, 요중 잠혈검사에서는 Combur-9-test RL이 가장 민감하였다.

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Remifentanil Protects Human Keratinocyte Through Autophagic Expression

  • Kim, Eok Nyun;Park, Chang Hoon;Woo, Mi Na;Yoon, Ji Young;Park, Bong Soo;Kim, Yong Ho;Kim, Cheul Hong
    • 대한치과마취과학회지
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    • 제14권2호
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    • pp.101-106
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    • 2014
  • Background: Remifentanil, an ultra-short-acting mu-opioid receptor agonist, is unique from other opioids because of its esterase-based metabolism, minimal accumulation, and very rapid onset and offset of clinical action. Remifentanil can prevent the inflammatory response and can suppress inducible nitric oxide synthase expression in a septic mouse model. However, the effects of remifentanil on human keratinocyte and autophagy have yet to be fully elucidated during hypoxia-reoxygenation. Here we investigated whether remifentanil confers protective effect against hypoxia-reoxygenation in human keratinocyte and, if so, whether autophagy mediates this effect. Methods: The human keratinocytes were cultured under 1% oxygen tension. The cells were gassed with 94% $N_2$, and 5% $CO_2$ and incubated for 24 h at $37^{\circ}C$. To determine whether the administration of affects human keratinocytes hypoxia-reoxygenation injury, cells were then exposed to various concentrations of remifentanil (0.01, 0.1, 0.5 and 1 ng/ml) for 2 h. After remifentanil treatment, to simulate reoxygenation and recovery, the cells were reoxygenated for 12 h at $37^{\circ}C$. Control group did not receive remifentanil treatment. Normoxia group did not receive hypoxia and remifentanil treatment for 36 h. 3-MA group was treated 3-methyladenine (3-MA) for 1h before remifentanil treatment. Cell viability was measured using a quantitative colorimetric assay with MTT, showing the mitochondrial activity of living cells. Cells were stained with fluorescence and analyzed with Western blot analysis to find out any relations with activation of autophagy. Results: Prominent accumulation of autophagic specific staining MDC was observed around the nuclei in RPT group HaCaT cells. Similarly, AO staining, red fluorescent spots appeared in RPT group HaCaT cells, while the Normoxia, control and 3-MA groups showed mainly green cytoplasmic fluorescence. We here examined activation of autophagy related protein under H/R-induced cells by Western blotting analysis. Atg5, Beclin-1, LC3-II (microtubule-associated protein 1 light chain 3 form II) and p62 was elevated in RPT group cells. But they were decreased when autophagy was suppressed by 3-MA (Fig. 5). Conclusions: Although the findings of this study are limited to an in vitro interpretation, we suggest that remifentanil may have a beneficial effect in the recovery of wound from hypoxia-reoxygenation injury.

Hydrolysis of Agricultural Residues and Kraft Pulps by Xylanolytic Enzymes from Alkaliphilic Bacillus sp. Strain BK

  • Kaewintajuk Kusuma;Chon Gil-Hyong;Lee Jin-Sang;Kongkiattikajorn Jirasak;Ratanakhanokchai Khanok;Kyu Khin Lay;Lee John-Hwa;Roh Min-Suk;Choi Yun-Young;Park Hyun;Lee Yun-Sik
    • Journal of Microbiology and Biotechnology
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    • 제16권8호
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    • pp.1255-1261
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    • 2006
  • An alkaliphilic bacterium, Bacillus sp. strain BK, was found to produce extracellular cellulase-free xylanolytic enzymes with xylan-binding activity. Since the pellet-bound xylanase is eluted with 2% TEA from the pellet of the culture, they contain a xylan-binding region that is stronger than the xylan-binding xylanase of the extracellular enzyme. The xylanases had a different molecular weight and xylan-binding ability. The enzyme activity of xylanase in the extracellular fraction was 6 times higher than in the pellet-bound enzyme. Among the enzymes, xylanase had the highest enzyme activity. When Bacillus sp. strain BK was grown in pH 10.5 alkaline medium containing xylan as the sole carbon source, the bacterium produced xylanase, arabinofuranosidase, acetyl esterase, and $\beta$-xylosidase with specific activities of 1.23, 0.11, 0.06, and 0.04 unit per mg of protein, respectively. However, there was no cellulase activity detected in the crude enzyme preparation. The hydrolysis of agricultural residues and kraft pulps by the xylanolytic enzymes was examined at 50$^{\circ}C$ and pH 7.0. The rate of xylan hydrolysis in com hull was higher than those of sugarcane bagasse, rice straw, com cop, rice husk, and rice bran. In contrast, the rate of xylan hydrolysis in sugarcane pulp was 2.01 and 3.52 times higher than those of eucalyptus and pine pulp, respectively. In conclusion, this enzyme can be used to hydrolyze xylan in agricultural residues and kraft pulps to breach and regenerate paper from recycled environmental resources.

Effects of stale maize on growth performance, immunity, intestinal morphology and antioxidant capacity in broilers

  • Liu, J.B.;Yan, H.L.;Zhang, Y.;Hu, Y.D.;Zhang, H.F.
    • Asian-Australasian Journal of Animal Sciences
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    • 제33권4호
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    • pp.605-614
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    • 2020
  • Objective: This study was conducted to determine the effects of stale maize on growth performance, immunity, intestinal morphology, and antioxidant capacity in broilers. Methods: A total of 800 one-day-old male Arbor Acres broilers (45.4±0.5 g) were blocked based on body weight, and then allocated randomly to 2 treatments with 20 cages per treatment and 20 broilers per cage in this 6-week experiment. Dietary treatments included a basal diet and diets with 100% of control maize replaced by stale maize. Results: The content of fat acidity value was higher (p<0.05) while the starch, activities of catalase and peroxidase were lower (p<0.05) than the control maize. Feeding stale maize diets reduced (p<0.05) average daily feed intake (ADFI) throughout the experiment, feed conversion ratio (FCR) during d 0 to 21 and the whole experiment as well as relative weight of liver, spleen, bursa of Fabricius and thymus (p<0.05) on d 21. Feeding stale maize diets decreased jejunum villus height (VH) and VH/crypt depth (CD) (p<0.05) on d 21 and 42 as well as ileum VH/CD on d 42. The levels of immunoglobulin G, acid α-naphthylacetate esterase positive ratios and lymphocyte proliferation on d 21 and 42 as well as lysozyme activity and avian influenza antibody H5N1 titer on d 21 decreased (p<0.05) by the stale maize. Feeding stale maize diets reduced (p<0.05) serum interferon-γ, tumor necrosis factor-α, interleukin-2 on d 21 and interleukin-6 on d 21 and 42. Broilers fed stale maize diets had lower levels of (p<0.05) total antioxidative capacity on d 42, superoxide dismutase and glutathione peroxidase on d 21 and 42, but higher (p<0.05) levels of malondialdehyde on d 21 and 42. Conclusion: Feeding 100% stale maize decreased ADFI and FCR, caused adverse effects on immunity and antioxidant function and altered intestinal morphology in broilers.