• 제목/요약/키워드: biochemical activity

검색결과 1,646건 처리시간 0.023초

HEPATO-AND RENAL TOXICITY OF AQUEOUS EXTRACT OF A MUSHROOM, AMANITA VOLVATA IN MICE

  • Chang, Il-Moo;Kazumasa Yokoyama;Yuji Ishihara;Morio Fukuara
    • Toxicological Research
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    • 제5권1호
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    • pp.1-7
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    • 1989
  • Toxic effects of a mushroom, Amanita volvata, were studied in respect to biochemical and histological changes induced in the liver and kidneys of mice. The changes in biochemical parameters characteristically appeared 12 hrs after oral administration of an aqueous extract of the mushroom. The hepatic glycogen decreased markedly to 17% of the control level and a concemitant decrease in blood glucose was also observed. The activity of serum glutamic oxaloacetic transaminase (SGOT) was elevated by 2.5-fold and the level of blood urea nitrogen (BUN) increased by 3-fold, respectively, 12 hrs after administration of the mushroom, their levels being maintained up to 24 hrs.

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Crystal Structure and Functional Characterization of a Cytochrome P450 (BaCYP106A2) from Bacillus sp. PAMC 23377

  • Kim, Ki-Hwa;Lee, Chang Woo;Dangi, Bikash;Park, Sun-Ha;Park, Hyun;Oh, Tae-Jin;Lee, Jun Hyuck
    • Journal of Microbiology and Biotechnology
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    • 제27권8호
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    • pp.1472-1482
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    • 2017
  • Bacterial cytochrome P450 (CYP) steroid hydroxylases are effectively useful in the pharmaceutical industry for introducing hydroxyl groups to a wide range of steroids. We found a putative CYP steroid hydroxylase (BaCYP106A2) from the bacterium Bacillus sp. PAMC 23377 isolated from Kara Sea of the Arctic Ocean, showing 94% sequence similarity with BmCYP106A2 (Bacillus megaterium ATCC 13368). In this study, soluble BaCYP106A2 was overexpressed to evaluate its substrate-binding activity. The substrate affinity ($K_d$ value) to 4-androstenedione was $387{\pm}37{\mu}M$. Moreover, the crystal structure of BaCYP106A2 was determined at $2.7{\AA}$ resolution. Structural analysis suggested that the ${\alpha}8-{\alpha}9$ loop region of BaCYP106A2 is intrinsically mobile and might be important for initial ligand binding. The hydroxyl activity of BaCYP106A2 was identified using in vitro enzyme assays. Its activity was confirmed with two kinds of steroid substrates, 4-androstenedione and nandrolone, using chromatography and mass spectrometry methods. The main products were mono-hydroxylated compounds with high conversion yields. This is the second study on the structure of CYP106A steroid hydroxylases, and should contribute new insight into the interactions of bacterial CYP106A with steroid substrates, providing baseline data for studying the CYP106A steroid hydroxylase from the structural and enzymatic perspectives.

Radiomodifying Potential of Panax ginseng in Liver of Swiss Albino Mice against Gamma Radiation

  • Sharma, Mukesh Kumar;Kumar, Madhu;Kumar, Ashok
    • Journal of Ginseng Research
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    • 제28권2호
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    • pp.78-86
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    • 2004
  • Panax ginseng occupies an important role in the folk medicine of China, Korea and Japan. The present study was undertaken to determine the radioprotective efficacy of ginseng root extract in the liver of Swiss albino mice. The animals were divided into 4 groups. Group I-Only vehicle was administered. Group II-The animals received 10 mg/kg body weight ginseng root extract i.p. for 4 consecutive days. Group III-Animals were irradiated with 8Gy gamma radiation at the dose rate of 1.69 Gy/min at the distance of 80 ems. Group IV-Animals were given by ginseng root extract (10 mg/kg body weight) continuously for 4 days and on 4th day they were irradiated with 8 Gy gamma radiation after 30 min. The animals from above groups were autopsied on 1,3,7,14 and 30 days. Biochemical estimations of phosphatases (acid & alkaline), LDH (lactate dehydrogenase), LPO (lipid peroxidation) and GSH (reduced glutathione) in liver and SGOT (serum glutamate oxaloacetate transaminase), SGPT (serum glutamate pyruvate transaminase) and alkaline phosphatase in serum were done. In ginseng treated group acid phosphatase (ACP), alkaline phosphatase (ALP), LPO and LDH in liver and SGOT, SGPT and alkaline phosphatase in serum did not show any significant alteration. However, a significant increase in GSH content in liver was recorded. In irradiated group there was a significant increase in ACP, ALP and LPO content in liver and SGOT & SGPT in serum was noted. Whereas, a significant decrease was recorded in GSH and LDH activity in liver and alkaline phosphatase activity in serum. Pretreatment of ginseng with radiation significantly alters the biochemical parameters in liver and serum. A significant decline in ACP, ALP activity and LPO content in liver and SGOT and SGPT activity in serum was observed. However, a significant increase in GSH content and LDH activity in liver and ALP activity in serum was estimated. The present study suggests that pretreatment of ginseng before irradiation significantly protects the liver and maintains the enzyme activity.

Phosphorylation on the PPP2R5D B regulatory subunit modulates the biochemical properties of protein phosphatase 2A

  • Yu, Un-Young;Ahn, Jung-Hyuck
    • BMB Reports
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    • 제43권4호
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    • pp.263-267
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    • 2010
  • To characterize the biochemical properties of the PP2A regulatory B subunit, PPP2R5D, we analyzed its phosphorylation sites, stoichiometry and effect on holoenzyme activity. PPP2R5D was phosphorylated on Ser-53, Ser-68, Ser-81, and Ser-566 by protein kinase A, and mutations at all four of these sites abolished any significant phosphorylation in vitro. In HEK293 cells, however, the Ser-566 was the major phosphorylation site after PKA activation by forskolin, with marginal phosphorylation on Ser-81. Inhibitory tyrosine phosphorylation on Tyr-307 of the PP2A catalytic C subunit was decreased after forskolin treatment. Kinetic analysis showed that overall PP2A activity was increased with phosphorylation by PPP2R5D phosphorylation. The apparent Km was reduced from $11.25\;{\mu}M$ to $1.175\;{\mu}M$ with PPP2R5D phosphorylation, resulting in an increase in catalytic activity. These data suggest that PKA-mediated activation of PP2A is enabled by PPP2R5D phosphorylation, which modulates the affinity of the PP2A holoenzyme to its physiological substrates.

EROD-microbioassay에 의한 학교 소각로 잔재 중 다이옥신 유사물질의 측정 (Determination of Dioxin-like Components in the School Waste Incinerator Residues by EROD-microbioassay)

  • 정규혁;오승민;윤완진
    • 한국환경보건학회지
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    • 제26권3호
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    • pp.11-17
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    • 2000
  • There are among the most relevant toxic emissions from incinerators such as polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), dioxin-like polychlorinated biphenyls (PCBs). Induction of cytochrome P4501A1 catalyzed 7-ethoxyresorufin O-deethylase(EROD) activity in mammalian cell culture(EROD bioassay) is thought to be a selective and sensitive parameter used for the quantification of dioxin-like components. In this study, the toxic emissions from several school waste incinerators were evaluated by determination of CYPIA catalytic activity and cytotoxicity using cell culture microbioassay. The incinerator residue and soil samples were collected from the schools located in Kyunggi province from April to June 1999. The samples were extracted in a Soxhlet apparatus using toluene for 20 hours. In order to clean-up, concentrated crude extracts were applied to basic alumina column. The EROD activities of extracts in the H4IIE cells were from 1.91$\pm$0.32 ng-TEQ/g to 24.54$\pm$3.48 ng-TEQ/g of biochemical-TEQ value. In soil samples, CYP1A catalytic activity was 0.09~0.64 ng-TEQ/g. EROD bioassay, seems to be a useful short-term bioassay when information about the biological response of complex environmental samples is needed. Although further study is needed, these results indicate that the potent toxic emissions are produced from school waste semi-incinerators.

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α-Galactosidase를 생산하는 고온성 Bacillus coagulans KM-1 균주의 생화학적 특성 (Biochemical Characterization of α-Galactosidase-Producing Thermophilic Bacillus coagulans KM-1)

  • 남기호;장미순;박희연;이레나 코네바
    • 한국수산과학회지
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    • 제47권5호
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    • pp.516-521
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    • 2014
  • A bacterium producing ${\alpha}$-galactosidase (${\alpha}$-$\small{D}$-galactoside galactohydrolase, EC 3.2.1.22) was isolated. The isolate, KM-1 was identified as Bacillus coagulans based on its 16S rRNA sequence, morphology, and biochemical properties. ${\alpha}$-Galactosidase activity was detected the culture supernatant of B. coagulans KM-1. The bacterium showed the maximum activity for hydrolyzing para-nitrophenyl-${\alpha}$-$\small{D}$-galactopyranoside (pNP-${\alpha}Gal$) at pH 6.0 and $50^{\circ}C$. It hydrolyzed oligomeric substrates such as melibiose, raffinose, and stachyose liberating a galactose residue, indicating that the B. coagulans KM-1 ${\alpha}$-galactosidase hydrolyzed ${\alpha}$-1,6 linkage. The results suggest that the decreased stachyose and raffinose contents in fermented soybean meal are due to the ${\alpha}$-galactosidase activity.

Cypermethrin과 Piperonyl butoxide가 rat의 독성반응에 미치는 영향 (Effect of Cypermethrin and Piperonyl Butoxide on Toxic Response in Rats)

  • 정규혁;홍사욱
    • 약학회지
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    • 제34권2호
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    • pp.69-79
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    • 1990
  • The aim of this experiment is to observe the toxicity of cypermethrin[S, R- -cyano-3-phenoxybenzyl-(1R, 1s, cis, trans)-2,2-dimethyl-3-(2,2-dichlorovinyl) cyclopropane carboxylate]and to investigate the synergistic effect of piperonyl butoxide on the cypermethrin toxicity. In cypermethrin (CYP) treated group, the biochemical parameters such as ALT, LDH, glucose in serum were remarkably elevated. The content of cytochrome P-450 and activity of NADPH-cytochrome c reductase in renal microsomal fraction were increased but those in hepatic microsomal fraction were not significantly increased. The activity of aniline hydroxylase and ATPase in liver were decreased. In the case of CYP plus piperonyl butoxide (PB) treated group, AST, ALT, LDH and glucose were more increased. Cytochrome P-450 and NADPH-cytochrome c reductase in liver and kidney were supressed and aniline hydroxylase and ATPase in liver were more decreased. Especially, in the case of CYP plus PB 100 mg/kg treated group, hepatic TBA value was increased but activity of glucose-6-phosphatase was remarkably depressed.

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토마토 Locular Fluid Lectin의 생화학적 성질 (Biochemical Properties of Locular Fluid Lectin of Tomato)

  • 노광수
    • KSBB Journal
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    • 제23권1호
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    • pp.48-53
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    • 2008
  • 토마토의 locular fluid로부터 최종적으로 Sephadex G-200 affinity chromatography에 의해 lectin을 분리한 다음, 이들의 분자량, 적혈구 응집력, 혈액특이성, 열 안정성, 최적 온도 및 pH 안정성의 생화학적 성질을 연구하였다. SBS-PAGE의 결과, 분자량이 39 kDa와 23 kDa로서 각각 2개의 subunit로 구성된 124 kDa의 분자량을 가지는 tetramer이다. 트립신으로 처리된 사람의 A, B, O, AB형의 혈액을 사용하여 각각의 혈구응집반응을 확인한 결과, A, B, O, AB형 모두에서 응집반응이 일어났으며, 이 중 B형 혈액에서 가장 높은 활성을 나타냈으며, A와 O형은 중간, AB형은 가장 낮은 활성을 보였다. 분리된 토마토 locular fluid의 최적반응 온도는 $50^{\circ}C$로서, 가장 높은 $70^{\circ}C$를 포함하는 $40-80^{\circ}C$에서 열 안정성을 보였으며, 이의 최적 pH는 7.0이다.

담배잎의 노화과정에 따른 단백질의 생화학적 변화 (Biochemical Changes of Protein during the Senescence of Tobacco Leaf)

  • 이상각;심상인;강병화
    • 한국작물학회지
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    • 제41권5호
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    • pp.563-568
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    • 1996
  • 담배 생육단계별 RNA, protease 활성도와 단백질 패턴의 변화를 파악하여 노화가 진행되는 과정에서 생리 ㆍ생화학적인 변화의 기초자료를 얻고자 본 실험을 수행하였으며 결과는 다음과 같다. 가용성 단백질 함량은 출엽 후 15일까지 증가하여 출엽 후 35일까지 일정하게 유지하였다. 총 RNA 함량은 출엽 후 15일에 가장 높았으며 출엽후 30일까지 급격한 감소를 보였다. Protease 활성 변화는 중성 protease (pH 7.8)가 활성이 높았으며 노화말기인 출엽 후 50일부터 갑자기 증가하였다. 전기영동 패턴은 큰 변화가 없었으나 61.0kd의 polypeptide은 출엽 후 35일부터 생성되어 노화말기까지 증가하였다.

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Biochemical Properties of Acetylcholinesterase from the Larval Head of Bombyx mori

  • Lee, Hwa-Jun;Lee, Heui-Sam;Lee, Pyeong-Jae;Cho, Il-Je;Lee, Sang-Mong;Moon, Jae-Yu
    • International Journal of Industrial Entomology and Biomaterials
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    • 제1권1호
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    • pp.73-78
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    • 2000
  • We investigated some biochemical properties of acetylcholinesterase (AChE) in the Bombyx mori larval head. 1% Triton X-100 (v/v) was suitable for extracting AChE from the silkworm larval head but 1 M NaCl was not suitable. PAGE analysis showed a single band of AChE that was detected by histochemical staining using acetylthiocholine as a substrate. AChE was also partially purified with Sepharose 6B and DEAE-cellulose column. Finally, the specific activity of partially purified enzyme solution was 7.6. The study on inhibitor specificity indicated that the enzyme under study was a true cholinesterase (ChE) or AChE. AChE activity was maximum at the substrate concentration of $5{\times}10^{-4}$ M and the excess substrate inhibited the AChE activity. The optimal pH and temperature were pH 7.0-9.0 and 30-35$^{\circ}C$.

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