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红树植物叶片中的吡啶补救途径和烟酸缀合物的合成。

Pyridine salvage and nicotinic acid conjugate synthesis in leaves of mangrove species.

机构信息

Department of Biological Sciences, Graduate School of Humanities and Sciences, Ochanomizu University, 2-1-1 Otsuka, Bunkyo-ku, Tokyo 112-8610, Japan.

出版信息

Phytochemistry. 2010 Jan;71(1):47-53. doi: 10.1016/j.phytochem.2009.09.033. Epub 2009 Nov 11.

Abstract

The metabolic fate of [carbonyl-14C]nicotinamide was surveyed in leaf disks of seven mangrove species, Bruguiera gymnorrhiza, Rhizophora stylosa, Kandeliaobovata, Sonneratia alba, Pemphis acidula, Lumnitzera racemosa and Avicennia marina, with and without 250 mM NaCl. Uptake of [14C]nicotinamide by leaf disks was stimulated by 250 mM NaCl in K. candel, R. stylosa, A. marina and L. racemosa. [Carbonyl-14C]nicotinamide was converted to nicotinic acid and was utilised for the synthesis of nucleotides and nicotinic acid conjugates. Formation of nicotinic acid by the deaminase reaction was rapid; there was little accumulation of nicotinamide in the disks 3h after administration. Radioactivity from [carbonyl-14C]nicotinamide was incorporated into pyridine nucleotides (mainly NAD and NADP) in all mangrove leaves, and the rates varied from 2% (in L. racemosa) to 15% (S. alba) of the total radioactivity taken up. NaCl generally reduced nicotinic acid salvage for NAD and NADP. In all mangrove leaf disks, the most heavily labelled compounds (up to 70% of total radioactivity) were trigonelline (N-methylnicotinic acid) and/or nicotinic acid N-glucoside. Trigonelline was formed in all mangrove plants, but N-glucoside synthesis was found only in leaves of A. marina and K. obovata. In A. marina, incorporation of radioactivity into N-glucoside (51%) was much greater than incorporation into trigonelline (2%). In general, NaCl stimulates the synthesis of these pyridine conjugates. The rate of decarboxylation of nicotinic acid in roots of A. marina seedlings was much greater than for the corresponding reaction observed in leaves.

摘要

[羰基-14C]烟酰胺在七种红树植物叶片中的代谢命运进行了研究,这七种植物分别是:木榄(Bruguiera gymnorrhiza)、桐花树(Rhizophora stylosa)、白骨壤(Kandelia obovata)、海桑(Sonneratia alba)、水黄皮(Pemphis acidula)、卤蕨(Lumnitzera racemosa)和尖瓣海莲(Avicennia marina),同时研究了有无 250mM NaCl 两种情况。在 K. candel、R. stylosa、A. marina 和 L. racemosa 中,250mM NaCl 刺激叶片对 [14C]烟酰胺的摄取。[羰基-14C]烟酰胺转化为烟酸,并用于核苷酸和烟酸缀合物的合成。脱氨酶反应迅速形成烟酸;给药 3 小时后,叶片中烟酰胺积累很少。[羰基-14C]烟酰胺的放射性掺入所有红树叶片的吡啶核苷酸(主要是 NAD 和 NADP)中,速率从 2%(在卤蕨中)到 15%(在海桑中)不等,占总放射性的比例。NaCl 通常会减少烟酸对 NAD 和 NADP 的回收利用。在所有红树叶片中,标记化合物最多(占总放射性的 70%)的是葫芦巴碱(N-甲基烟酸)和/或烟酸 N-葡萄糖苷。在所有红树植物中都形成了葫芦巴碱,但仅在 A. marina 和 K. obovata 的叶片中发现了 N-葡萄糖苷的合成。在 A. marina 中,放射性物质掺入 N-葡萄糖苷(51%)的速率远高于掺入葫芦巴碱(2%)的速率。总的来说,NaCl 刺激这些吡啶缀合物的合成。A. marina 幼苗根中的烟酸脱羧率远高于叶片中的相应反应。

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