Andralojc P J, Dawson G W, Parry M A, Keys A J
Institute of Arable Crops Research, Rothamsted Experimental Station, Harpenden, Hertfordshire, U.K.
Biochem J. 1994 Dec 15;304 ( Pt 3)(Pt 3):781-6. doi: 10.1042/bj3040781.
The synthesis of 2-carboxy-D-arabinitol-1-phosphate (CA1P), the naturally occurring inhibitor of ribulose-1,5-bisphosphate carboxylase/oxygenase, was studied in leaves of the French bean Phaseolus vulgaris, L. Leaves were supplied with air containing 14CO2 in the light then the plants were transferred to normal air in the light or in the dark. Leaf samples were frozen in liquid nitrogen, ground to a powder and extracted with acid. Lipids, pigments and cations were removed from the extract and CA1P and 2-carboxy-D-arabinitol (CA) recovered by anion exchange chromatography. The CA1P was further purified by its specific binding to purified ribulose-1,5-bisphosphate carboxylase/oxygenase. CA and CA1P were identified by chromatographic properties and n.m.r. spectra. When plants were kept for 15 h in darkness after exposure to 14CO2, up to 2.2% and 5.5% of the radioactivity in the extracts was present in CA1P and CA, respectively. The most radioactivity appeared in these compounds when photosynthesis from 14CO2 took place at low photosynthetic photon flux density (PPFD). Under such conditions, radioactivity was detected in CA1P after only 10 min. During subsequent exposure to normal air (12CO2) at low PPFD the amount of radioactivity in CA1P remained almost constant for 6 h; in darkness the rate of incorporation of radioactivity into CA1P reached a maximum after 2 h and the radioactivity was still increasing 6 h later. At low PPFD, the amount of CA1P in the leaves reached a maximum after 2 h. In darkness, the amount of CA1P began to increase rapidly after a lag of almost 1 h, well ahead of the increase in radioactivity in CA1P.
对2-羧基-D-阿拉伯糖醇-1-磷酸(CA1P)的合成进行了研究,CA1P是核酮糖-1,5-二磷酸羧化酶/加氧酶的天然抑制剂,研究对象为法国菜豆(Phaseolus vulgaris, L.)的叶片。在光照条件下,向叶片供应含14CO2的空气,然后将植株转移至正常空气中,光照或黑暗条件均可。将叶片样品在液氮中冷冻,研磨成粉末并用酸提取。从提取物中去除脂质、色素和阳离子,通过阴离子交换色谱法回收CA1P和2-羧基-D-阿拉伯糖醇(CA)。通过其与纯化的核酮糖-1,5-二磷酸羧化酶/加氧酶的特异性结合进一步纯化CA1P。通过色谱性质和核磁共振光谱鉴定CA和CA1P。在暴露于14CO2后,植株在黑暗中放置15小时,提取物中分别有高达2.2%和5.5%的放射性存在于CA1P和CA中。当在低光合光子通量密度(PPFD)下进行14CO2光合作用时,这些化合物中出现的放射性最多。在这种条件下,仅10分钟后就在CA1P中检测到放射性。在随后低PPFD条件下暴露于正常空气(12CO2)期间,CA1P中的放射性量在6小时内几乎保持不变;在黑暗中,放射性掺入CA1P的速率在2小时后达到最大值,6小时后放射性仍在增加。在低PPFD下,叶片中CA1P的量在2小时后达到最大值。在黑暗中,CA1P的量在几乎1小时的滞后后开始迅速增加,远早于CA1P中放射性的增加。