Oxidation of ferrocytochrome c by lignin peroxidase.

Oxidation of ferrocytochrome c by lignin peroxidase.
复制标题

木质素过氧化物酶氧化铁细胞色素 c。

DOI:
--
复制
发表时间:
1994
期刊:
影响因子:
2.9
通讯作者:
M. Gold
M. Gold
中科院分区:
生物学3区
文献类型:
--
作者:
H. Wariishi;D. Sheng;M. Gold

文献摘要

参考文献

被引文献

相似文献

我们证明直接氧化亚铁细胞色素c的木质素过氧化物酶(LiP)从木质素降解的担子菌,黄孢原毛革菌。稳态动力学数据符合过氧化物酶乒乓机制,而不是有序的双-双乒乓机制,这表明铁细胞色素c减少LiP化合物I和II是不可逆的。整个反应的pH依赖性显然是由两个因素控制,电子转移速率的pH依赖性和在H2 O2存在下酶失活的pH依赖性。在100 μ M H2 O2的存在下,藜芦醇(VA)显着增强细胞色素c氧化在pH 3.0,但在pH 4.5以上的影响不大。在< 10 μ M H_2O_2存在下,VA对反应的刺激作用大大减弱。与细胞色素c过氧化物酶的反应,LiP氧化亚铁细胞色素c的离子强度增加,这意味着参与的聚合物底物和酶之间的静电相互作用。反应产物铁细胞色素C抑制VA氧化LiP在一个非竞争性的方式,这表明细胞色素C结合LiP在一个网站不同的小芳香底物结合位点。最近的晶体学研究表明,血红素是埋在LiP蛋白质和不可用的直接相互作用与聚合物基板,这表明电子转移从铁细胞色素c LiP发生在一个相对较长的范围。讨论了VA在该电子转移反应中的作用。(250字处删节)
We demonstrate direct oxidation of ferrocytochrome c by lignin peroxidase (LiP) from the lignin-degrading basidiomycete, Phanerochaete chrysosporium. Steady-state kinetic data fit a peroxidase ping-pong mechanism rather than an ordered bi-bi ping-pong mechanism, suggesting that the reductions of LiP compounds I and II by ferrocytochrome c are irreversible. The pH dependence of the overall reaction apparently is controlled by two factors, the pH dependence of the electron-transfer rate and the pH dependence of enzyme inactivation in the presence of H2O2. In the presence of 100 microM H2O2, veratryl alcohol (VA) significantly enhanced cytochrome c oxidation at pH 3.0 but had little effect above pH 4.5. In the presence of < 10 microM H2O2, the stimulating effect of VA on the reaction is greatly diminished. As with cytochrome c peroxidase reactions, LiP oxidation of ferrocytochrome c decreased as the ionic strength increased, implying the involvement of electrostatic interactions between the polymeric substrate and enzyme. The reaction product ferricytochrome c inhibited VA oxidation by LiP in a noncompetitive manner, suggesting that cytochrome c binds to LiP at a site different from the small aromatic substrate binding site. Recent crystallographic studies show that the heme is buried in the LiP protein and unavailable for direct interaction with polymeric substrates, suggesting that electron transfer from ferrocytochrome c to LiP occurs over a relatively long range. The role of VA in this electron-transfer reaction is discussed.(ABSTRACT TRUNCATED AT 250 WORDS)
DOI: 10.1016/s0021-9258(17)35994-x
发表时间: 1986-02
期刊: The Journal of biological chemistry
影响因子: --
作者:
M. Tien;T. Kirk;C. Bull;J. Fee
通讯作者: M. Tien;T. Kirk;C. Bull;J. Fee
苯肼和叠氮化钠灭活木质素过氧化物酶。
DOI: 10.1016/0003-9861(90)90539-b
发表时间: 1990
影响因子: 3.9
作者:
DePillis,GD;Wariishi,H;Gold,MH;OrtizdeMontellano,PR
通讯作者: OrtizdeMontellano,PR
在藜芦醇、丙二酸或草酸以及氧气存在下,木质素过氧化物酶氧化 Mn2。
DOI: 10.1021/bi00498a008
发表时间: 1990
期刊: Biochemistry
影响因子: 2.9
作者:
Popp,JL;Kalyanaraman,B;Kirk,TK
通讯作者: Kirk,TK
DOI: 10.1126/science.1334573
发表时间: 1992-12-11
期刊: SCIENCE
影响因子: 56.9
作者:
PELLETIER, H;KRAUT, J
通讯作者: KRAUT, J
DOI: --
发表时间: 1982
期刊: The Journal of biological chemistry
影响因子: --
作者:
Kang,DS;Erman,JE
通讯作者: Erman,JE