Walters Kent R, Pan Qingfeng, Serianni Anthony S, Duman John G
From the Departments of Biological Sciences, Notre Dame, Indiana 46556.
Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556; Omicron Biochemicals, Inc., South Bend, Indiana 46617.
J Biol Chem. 2009 Jun 19;284(25):16822-16831. doi: 10.1074/jbc.M109.013870. Epub 2009 Apr 29.
Adult Upis ceramboides do not survive freezing in the summer but tolerate freezing to -60 degrees C in midwinter. The accumulation of two cryoprotective polyols, sorbitol and threitol, is integral to the extraordinary cold-hardiness of this beetle. U. ceramboides are the only animals known to accumulate high concentrations of threitol; however, the biosynthetic pathway has not been studied. A series of (13)C-labeled compounds was employed to investigate this biosynthetic pathway using (13)C{(1)H} NMR spectroscopy. In vivo metabolism of (13)C-labeled glucose isotopomers demonstrates that C-3-C-6 of glucose become C-1-C-4 of threitol. This labeling pattern is expected for 4-carbon saccharides arising from the pentose phosphate pathway. In vitro experiments show that threitol is synthesized from erythrose 4-phosphate, a C(4) intermediate in the PPP. Erythrose 4-phosphate is epimerized and/or isomerized to threose 4-phosphate, which is subsequently reduced by a NADPH-dependent polyol dehydrogenase and dephosphorylated by a sugar phosphatase to form threitol. Threitol 4-phosphate appears to be the preferred substrate of the sugar phosphatase(s), promoting threitol synthesis over that of erythritol. In contrast, the NADPH-dependent polyol dehydrogenase exhibits broad substrate specificity. Efficient erythritol catabolism under conditions that promote threitol synthesis, coupled with preferential threitol biosynthesis, appear to be responsible for the accumulation of high concentrations of threitol (250 mm) without concomitant accumulation of erythritol.
成年的赤拟谷盗在夏季无法在冷冻条件下存活,但在冬季中期能耐受零下60摄氏度的冷冻。两种抗冻多元醇,山梨醇和苏糖醇的积累,是这种甲虫非凡抗寒能力的关键。赤拟谷盗是已知唯一能积累高浓度苏糖醇的动物;然而,其生物合成途径尚未得到研究。一系列碳-13标记的化合物被用于利用碳-13{氢}核磁共振光谱研究这条生物合成途径。碳-13标记的葡萄糖异构体的体内代谢表明,葡萄糖的C-3至C-6变成了苏糖醇的C-1至C-4。这种标记模式与磷酸戊糖途径产生的四碳糖类的预期相符。体外实验表明,苏糖醇由磷酸戊糖途径中的C4中间体4-磷酸赤藓糖合成。4-磷酸赤藓糖差向异构化和/或异构化为4-磷酸苏糖,随后被依赖NADPH的多元醇脱氢酶还原,并被糖磷酸酶去磷酸化形成苏糖醇。4-磷酸苏糖醇似乎是糖磷酸酶的首选底物,相比于赤藓醇,它更有利于促进苏糖醇的合成。相比之下,依赖NADPH的多元醇脱氢酶表现出广泛的底物特异性。在促进苏糖醇合成的条件下,赤藓醇能高效分解代谢,再加上优先的苏糖醇生物合成,似乎是高浓度苏糖醇(250 mM)积累而不伴随赤藓醇积累的原因。