首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Toward modeling the high chloride, low pH form of sulfite oxidase: Ka-band ESEEM of equatorial chloro ligands in oxomolybdenum(V) complexes
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Toward modeling the high chloride, low pH form of sulfite oxidase: Ka-band ESEEM of equatorial chloro ligands in oxomolybdenum(V) complexes

机译:建模高氯化物,低pH形式的亚硫酸盐氧化酶:氧钼(V)络合物中赤道氯配体的Ka波段ESEEM

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摘要

Two oxomolybdenum(V) complexes, (dttd)MoOCl and [(bdt)MoOCl(2)](-) (where dttd=2,3:8,9-dibenzo-1,4,7,10-tetrathiadecane and bdt=1,2-benzenedithiolate), which contain one or two equatorial chloro ligands, respectively, were studied by electron spin echo envelope modulation (ESEEM) spectroscopy in the microwave K(a)-band (approximately 29GHz). The ESEEM amplitude from the chloro ligands in both compounds is significantly greater than that tentatively attributed to chloride in the vicinity of the oxomolybdenum active site in the high chloride, low-pH (lpH) form of sulfite oxidase (SO). Thus, these ESEEM results rule out equatorial coordination of chloride in the enzyme, although the possibility for a weakly bound chloride in the trans axial position or nearby non-coordinated chloride(s) remains for lpH SO in solution.
机译:两种氧钼(V)配合物(dttd)MoOCl和[(bdt)MoOCl(2)](-)(其中dttd = 2,3:8,9-二苯并-1,4,7,10-四噻烷和bdt =通过电子自旋回波包络调制(ESEEM)光谱在微波K(a)波段(约29GHz)中研究了分别包含一个或两个赤道氯配体的1,2-苯二硫代)。两种化合物中来自氯配体的ESEEM幅度都明显大于暂定归因于亚硫酸盐氧化酶(SO)的高氯化物,低pH(lpH)形式的氧钼活性部位附近的氯化物。因此,这些ESEEM结果排除了酶中氯化物的赤道配位,尽管对于溶液中的1pH SO仍然存在跨轴向位置弱结合的氯化物或附近的未配位氯化物的可能性。

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