Katoh S, Sueoka T, Hikita H
Deptartment of Biochemistry, Meikai University School of Dentistry, Saitama, Japan.
J Nutr Sci Vitaminol (Tokyo). 1992;Spec No:497-500. doi: 10.3177/jnsv.38.special_497.
Computer simulation analysis of the experimental data showed that Cl'-keto PH4 and C2'-keto PH4 were sequential intermediates of the reduction of PPH4 to BH4 by SPR and that the reaction in the last step of the BH4 biosynthesis proceeds as follows: PPH4-->Cl'-keto PH4-->C2'-keto PH4-->BH4 Cl'-keto PH4 is not detectable in the reduction of PPH4 by the purified SPR at neutral pH since isomerization (-->) [8] may occur far more rapidly than the first reduction (-->).
对实验数据的计算机模拟分析表明,Cl'-酮基-PH4和C2'-酮基-PH4是SPR将PPH4还原为BH4过程中的连续中间体,并且BH4生物合成最后一步的反应如下:PPH4→Cl'-酮基-PH4→C2'-酮基-PH4→BH4。在中性pH条件下,纯化的SPR将PPH4还原时,Cl'-酮基-PH4无法检测到,因为异构化(-->[8])可能比首次还原(-->)快得多。