高等学校化学学报
高等學校化學學報
고등학교화학학보
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES
2014年
3期
476-481
,共6页
郑阿萍%王芳%邢蕊%蒋爱华%王力
鄭阿萍%王芳%邢蕊%蔣愛華%王力
정아평%왕방%형예%장애화%왕력
多金属氧酸盐%酪氨酸酶%非变性聚丙烯凝胶电泳%抑制作用
多金屬氧痠鹽%酪氨痠酶%非變性聚丙烯凝膠電泳%抑製作用
다금속양산염%락안산매%비변성취병희응효전영%억제작용
Polyoxometalate%Mushroom tyrosinase%Native polyacrylamide gel electrophoresis( PAGE)%Inhi-bition effect
以H3 PW12 O40和H4 SiW12 O40(简写为PW12和SiW12)为效应物,测定其对酪氨酸酶活力的抑制作用.通过非变性聚丙烯凝胶( Native-PAGE)电泳确定酪氨酸酶是多家族基因编码,其分子量为3×104~3.4×104,4.2×104~4.6×104,6.4×104~6.8×104,且均具有活性,测定PW12和SiW12对酪氨酸酶的抑制效果,并结合酶动力学法研究其抑制机理.结果表明,当PW12和SiW12浓度分别达到13和25 mmol/L时,酪氨酸酶的活力完全被抑制,即PW12和SiW12对酪氨酸酶二酚酶具有不同程度的抑制效果.当所加酶量为0.0173 mg/mL时, PW12和SiW12对酪氨酸酶二酚酶活力的半抑制率( IC50)分别为1.57和2.31 mmol/L,它们对酪氨酸酶二酚酶的抑制均为可逆过程.其中, PW12对二酚酶的抑制类型为混合型,其KI及KIS分别为0.34和0.43 mmol/L, SiW12对二酚酶的抑制类型表现为竞争型,其KI为0.59 mmol/L.综合考虑IC50值和抑制常数等参数, PW12对酪氨酸酶二酚酶的抑制能力优于SiW12.
以H3 PW12 O40和H4 SiW12 O40(簡寫為PW12和SiW12)為效應物,測定其對酪氨痠酶活力的抑製作用.通過非變性聚丙烯凝膠( Native-PAGE)電泳確定酪氨痠酶是多傢族基因編碼,其分子量為3×104~3.4×104,4.2×104~4.6×104,6.4×104~6.8×104,且均具有活性,測定PW12和SiW12對酪氨痠酶的抑製效果,併結閤酶動力學法研究其抑製機理.結果錶明,噹PW12和SiW12濃度分彆達到13和25 mmol/L時,酪氨痠酶的活力完全被抑製,即PW12和SiW12對酪氨痠酶二酚酶具有不同程度的抑製效果.噹所加酶量為0.0173 mg/mL時, PW12和SiW12對酪氨痠酶二酚酶活力的半抑製率( IC50)分彆為1.57和2.31 mmol/L,它們對酪氨痠酶二酚酶的抑製均為可逆過程.其中, PW12對二酚酶的抑製類型為混閤型,其KI及KIS分彆為0.34和0.43 mmol/L, SiW12對二酚酶的抑製類型錶現為競爭型,其KI為0.59 mmol/L.綜閤攷慮IC50值和抑製常數等參數, PW12對酪氨痠酶二酚酶的抑製能力優于SiW12.
이H3 PW12 O40화H4 SiW12 O40(간사위PW12화SiW12)위효응물,측정기대락안산매활력적억제작용.통과비변성취병희응효( Native-PAGE)전영학정락안산매시다가족기인편마,기분자량위3×104~3.4×104,4.2×104~4.6×104,6.4×104~6.8×104,차균구유활성,측정PW12화SiW12대락안산매적억제효과,병결합매동역학법연구기억제궤리.결과표명,당PW12화SiW12농도분별체도13화25 mmol/L시,락안산매적활력완전피억제,즉PW12화SiW12대락안산매이분매구유불동정도적억제효과.당소가매량위0.0173 mg/mL시, PW12화SiW12대락안산매이분매활력적반억제솔( IC50)분별위1.57화2.31 mmol/L,타문대락안산매이분매적억제균위가역과정.기중, PW12대이분매적억제류형위혼합형,기KI급KIS분별위0.34화0.43 mmol/L, SiW12대이분매적억제류형표현위경쟁형,기KI위0.59 mmol/L.종합고필IC50치화억제상수등삼수, PW12대락안산매이분매적억제능력우우SiW12.
H3 PW12 O40 and H4 SiW12 O40 ( abbreviated as PW12 and SiW12 ) were taken as inhibitors and their inhibitory effects and mechanisms on mushroom tyrosinase were evaluated by Native polyacrylamide gel electro-phoresis( PAGE) electrophoresis method and kinetic enzymatic method. The Native-PAGE electrophoresis re-sults show that tyrosinase are encoded by a multigene family, their molecular weight are mainly 3í104-3.4í104 , 4.2í104-4.6í104 and 6.4í104-6.8í104 , which were all active. The inhibitory effects of Kiggin-type polyoxotungstates, H3 PW12 O40 and H4 SiW12 O40 on mushroom tyrosinase were evaluated, and then the inhibito-ry mechanisms were further studied combined with the kinetic enzymatic method. The results indicated that the enzyme was inactive when the concentration of PW12 and SiW12 was 13 and 25 mmol/L, respectively. More-over, the kinetic enzymatic method suggested that both PW12 and SiW12 exhibited potent inhibitory activities with IC50 value of 1.57 and 2.31 mmol/L, respectively. PW12 was found to be a mixed-type inhibitor with KI=0.34 mmol/L and KIS=0.43 mmol/L, while SiW12 was suggested to be competitive inhibitor of tyrosinase with KI of 0.59 mmol/L. Based on a comprehensive consideration of IC50 and inhibitory constants, PW12 was more effective against mushroom tyrosinase than SiW12 .