首页> 美国卫生研究院文献>Biochemical Journal >Synthesis of retinyl phosphate mannose and dolichyl phosphate mannose from endogenous and exogenous retinyl phosphate and dolichyl phosphate in microsomal fraction. Specific decrease in endogenous retinyl phosphate mannose synthesis in vitamin A deficiency.
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Synthesis of retinyl phosphate mannose and dolichyl phosphate mannose from endogenous and exogenous retinyl phosphate and dolichyl phosphate in microsomal fraction. Specific decrease in endogenous retinyl phosphate mannose synthesis in vitamin A deficiency.

机译:由内源性和外源性磷酸视黄酯和磷酸二氢甲酯以微粒体级分合成磷酸视黄酯磷酸甘露糖和磷酸二氢甲酯甘露糖。维生素A缺乏症中内源性磷酸视黄酯磷酸甘露糖合成的特异性降低。

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摘要

Rat liver microsomal fraction synthesized Ret-P-Man (retinyl phosphate mannose) and Dol-P-Man (dolichyl phosphate mannose) from endogenous Ret-P (retinyl phosphate) and Dol-P (dolichyl phosphate). Ret-P-Man synthesis displayed an absolute requirement for a bivalent cation, and also Dol-P-Man synthesis was stimulated by bivalent metal ions. Mn2+ and Co2+ were the most active, with maximum synthesis of Ret-P-Man occurring at 5-10 mM: Mg2+ was also active, but at higher concentrations. At 5mM-Mn2+ the amount of endogenous Ret-P mannosylated in incubation mixtures containing 5 microM-GDP-mannose in 15 min at 37 degrees C was approx. 3 pmol/mg of protein. In the same assays about 7-10 pmol of endogenous Dol-P was mannosylated. Bivalentcation requirement for Ret-P-Man synthesis from exogenous Ret-P showed maximum synthesis at 2.5 mM-Mn2+ or -Co2+. In addition to Ret-P-Man and Dol-P-Man, a mannolipid co-chromatographing with undecaprenyl phosphate mannose was detected. Triton X-100 (0.5%) abolished Ret-P-Man synthesis from endogenous Ret-P and caused a 99% inhibition of Ret-P-Man synthesis from exogenous Ret-P. The presence of detergent (0.5%) also inhibited Dol-P-Man synthesis from endogenous Dol-P and altered the requirement for Mn2+. Microsomal fraction from Syrian golden hamsters was also active in Ret-P-Man and Dol-P-Man synthesis from endogenous Ret-P and Dol-P. At 5 mM-Mn2+ about 2.5 pmol of endogenous Ret-P and 3.7 pmol of endogenous Dol-P were mannosylated from GDP-mannose per mg of protein in 15 min at 37 degrees C. On the other hand, microsomal fraction from vitamin A-deficient hamsters contained 1.2 pmol of Ret-P and 14.1 pmol of Dol-P available for mannosylation. Since GDP-mannose: Ret-P and GDP-mannose: Dol-P mannosyltransferase activities were not affected, depletion of vitamin A must affect Ret-P and Dol-P pools in opposite ways.
机译:大鼠肝微粒体级分由内源性Ret-P(磷酸视黄酯)和Dol-P(磷酸二氢酯)合成Ret-P-Man(视黄磷酸磷酸甘露糖)和Dol-P-Man(磷酸二氢磷酸甘露糖)。 Ret-P-Man合成显示出对二价阳离子的绝对要求,而且Dol-P-Man合成也受到二价金属离子的刺激。 Mn2 +和Co2 +最具活性,Ret-P-Man的最大合成发生在5-10 mM:Mg2 +也具有活性,但浓度较高。在5mM-Mn2 +浓度下,在37°C下15分钟内,含有5 microM-GDP-甘露糖的孵育混合物中内源Ret-P甘露糖基化的量约为。 3 pmol / mg的蛋白质。在相同的测定中,约7-10 pmol的内源性Dol-P被甘露糖基化。从外源Ret-P合成Ret-P-Man的二价要求显示在2.5 mM-Mn2 +或-Co2 +处合成最大。除Ret-P-Man和Dol-P-Man外,还检测到用十一碳烯基磷酸甘露糖进行的甘露糖脂共色谱。 Triton X-100(0.5%)取消了内源Ret-P合成Ret-P-Man,并抑制了99%抑制外源Ret-P合成Ret-P-Man。去垢剂(0.5%)的存在也抑制了内源性Dol-P合成Dol-P-Man,并改变了对Mn2 +的需求。来自叙利亚金仓鼠的微粒体组分也活跃于由内源性Ret-P和Dol-P合成的Ret-P-Man和Dol-P-Man。在37°C的条件下,在15分钟内从GDP-甘露糖中每毫克蛋白质甘露糖基化了5 mM-Mn2 +约2.5 pmol内源性Ret-P和3.7 pmol内源性Dol-P。另一方面,维生素A-的微粒体部分缺乏的仓鼠含有1.2 pmol的Ret-P和14.1 pmol的Dol-P可用于甘露糖基化。由于GDP-甘露糖:Ret-P和GDP-甘露糖:Dol-P甘露糖基转移酶的活性未受影响,因此维生素A的消耗必须以相反的方式影响Ret-P和Dol-P库。

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