首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Leghemoglobin green derivatives with nitrated hemes evidence production of highly reactive nitrogen species during aging of legume nodules
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Leghemoglobin green derivatives with nitrated hemes evidence production of highly reactive nitrogen species during aging of legume nodules

机译:带有血红素化血红素的豆血红蛋白绿色衍生物证明在豆类小结节衰老过程中产生高反应性氮

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摘要

Globins constitute a superfamily of proteins widespread in all kingdoms of life, where they fulfill multiple functions, such as efficient O2 transport and modulation of nitric oxide bioactivity. In plants, the most abundant Hbs are the symbiotic leghemoglobins (Lbs) that scavenge O2 and facilitate its diffusion to the N2-fixing bacteroids in nodules. The biosynthesis of Lbs during nodule formation has been studied in detail, whereas little is known about the green derivatives of Lbs generated during nodule senescence. Here we characterize modified forms of Lbs, termed Lbam, Lbcm, and Lbdm, of soybean nodules. These green Lbs have identical globins to the parent red Lbs but their hemes are nitrated. By combining UV-visible, MS, NMR, and resonance Raman spectroscopies with reconstitution experiments of the apoprotein with protoheme or mesoheme, we show that the nitro group is on the 4-vinyl. In vitro nitration of Lba with excess nitrite produced several isomers of nitrated heme, one of which is identical to those found in vivo. The use of antioxidants, metal chelators, and heme ligands reveals that nitration is contingent upon the binding of nitrite to heme Fe, and that the reactive nitrogen species involved derives from nitrous acid and is most probably the nitronium cation. The identification of these green Lbs provides conclusive evidence that highly oxidizing and nitrating species are produced in nodules leading to nitrosative stress. These findings are consistent with a previous report showing that the modified Lbs are more abundant in senescing nodules and have aberrant O2 binding.
机译:球蛋白构成了生活中所有王国中广泛分布的蛋白质的超家族,它们履行多种功能,例如有效的O2转运和一氧化氮生物活性的调节。在植物中,最丰富的Hb是清除O2并促进其扩散到结节中固定N2的类细菌的共生豆球蛋白(Lbs)。已经详细研究了结节形成过程中Lbs的生物合成,而对结节衰老过程中产生的Lbs绿色衍生物知之甚少。在这里,我们表征大豆结节的Lbs的修饰形式,称为Lbam,Lbcm和Lbdm。这些绿色Lb与母红色Lb具有相同的珠蛋白,但它们的血红素已被硝化。通过结合紫外线可见光,质谱,核磁共振和共振拉曼光谱与载脂蛋白与原血红素或中血红素的重构实验相结合,我们表明硝基位于4-乙烯基上。用过量的亚硝酸盐对Lba进行体外硝化会产生硝化血红素的几种异构体,其中之一与体内发现的异构体相同。抗氧化剂,金属螯合剂和血红素配体的使用表明硝化取决于亚硝酸盐与血红素Fe的结合,所涉及的反应性氮物种源自亚硝酸,最有可能是硝基阳离子。对这些绿色Lb的鉴定提供了确凿的证据,表明结节中会产生高度氧化和硝化的物种,导致亚硝化胁迫。这些发现与先前的报告一致,该报告显示修饰的Lbs在致敏结节中更丰富,并且具有异常的O2结合。

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