Butler R N, Arora K K, Collins J G, Flanigan I, Lawson M J, Roberts-Thomson I C, Williams J F
Department of Gastroenterology, Queen Elizabeth Hospital, Woodville South, South Australia.
Biochem Int. 1990 Oct;22(2):249-60.
The colonic cells of the large intestine are one of the most proliferative tissues of the animal body. The pentose pathway has an essential role in cell division and growth being the only pathway forming ribose 5-P necessary for all nucleotide and nucleic acid sunthesis. The pentose pathway may also provide reducing potential as NADPH for biosynthesis and C-3- C-8 glycolyl compounds. The maximum catalytic capacities of the reactions of the non-oxidative pentose pathway for the conversion of ribose 5-P to hexose and triose phosphates by the proximal and distal colon under feeding and starvation regimes are among the highest in the animal body. The qualitative presence of the oxidative pentose pathway was assessed by measurement of the C-1/C-6 ratio value of 1.67-1.82. Enzymes of the F-type and L-type pentose pathways are present in colonocytes and their maximum catalytic activities in colonocyte cytosol are reported. The contribution of the F-type pentose cycle to the total glucose metabolism of colonocytes, measured by the specific yield method, is negligibly low (approximately 1.5%). Colonic epithelial cells use glucose at a high rate (7.1 +/- 0.33 mumol min-1g-1 dry wt) and 79% of the glucose is converted to lactate. Arabinose 5-P has an intermediary role in the formation of keto pentose, sedoheptulose and hexose phosphates from ribose 5-P by colonocyte cytosol. The intermediary and reaction products of [1-13C] ribose 5-P dissimilation by colonocytes is investigated by 13C NMR spectroscopy. The 13C positional isotope distributions show labelling of C-1 and C-3 of hexose 6-phosphates consistent with either the theoretical predictions of the F-type pentose pathway or of the activities of exchange reactions catalysed by transketolase and/or transaldolase. Measurements of exchange reactions showed that the C-1/C-3 labelling of these compounds is mostly, if not wholly, attributable to exchange catalysis by these group transferring enzymes. The results suggest that the F-type PC has little role in the glucose metabolism of colonocytes and pentose phosphate formation may thus occur by a contribution (approx 20% of the total glucose metabolism) by the alternate L-type pathway.
大肠的结肠细胞是动物体内增殖能力最强的组织之一。戊糖途径在细胞分裂和生长中起着至关重要的作用,是形成所有核苷酸和核酸合成所需的5-磷酸核糖的唯一途径。戊糖途径还可为生物合成和C-3 - C-8糖基化合物提供作为NADPH的还原电位。在进食和饥饿状态下,近端和远端结肠中戊糖非氧化途径将5-磷酸核糖转化为己糖和磷酸丙糖反应的最大催化能力在动物体内是最高的。通过测量C-1/C-6比值为1.67 - 1.82来评估氧化戊糖途径的定性存在。F型和L型戊糖途径的酶存在于结肠细胞中,并报道了它们在结肠细胞胞质溶胶中的最大催化活性。通过特定产率法测量,F型戊糖循环对结肠细胞总葡萄糖代谢的贡献极低(约1.5%)。结肠上皮细胞以高速率利用葡萄糖(7.1±0.33 μmol min-1g-1干重),并且79%的葡萄糖转化为乳酸。5-磷酸阿拉伯糖在结肠细胞胞质溶胶中由5-磷酸核糖形成酮戊糖、景天庚酮糖和磷酸己糖的过程中起中间作用。通过13C核磁共振光谱研究结肠细胞对[1-13C]5-磷酸核糖异化的中间产物和反应产物。13C位置同位素分布显示6-磷酸己糖的C-1和C-3标记与F型戊糖途径的理论预测或转酮醇酶和/或转醛醇酶催化的交换反应活性一致。交换反应的测量表明,这些化合物的C-1/C-3标记大多(如果不是全部)归因于这些基团转移酶的交换催化作用。结果表明,F型戊糖循环在结肠细胞的葡萄糖代谢中作用很小,因此戊糖磷酸的形成可能通过替代的L型途径贡献(约占总葡萄糖代谢的20%)而发生。