Corpas Francisco J, Barroso Juan B, Carreras Alfonso, Quirós Miguel, León Ana M, Romero-Puertas María C, Esteban Francisco J, Valderrama Raquel, Palma José M, Sandalio Luisa M, Gómez Manuel, del Río Luis A
Departamento de Bioquímica, Biología Celular y Molecular de Plantas, Consejo Superior de Investigaciones Científicas, E-18080 Granada, Spain.
Plant Physiol. 2004 Sep;136(1):2722-33. doi: 10.1104/pp.104.042812. Epub 2004 Sep 3.
The cellular and subcellular localization of endogenous nitric oxide (NO.) in leaves from young and senescent pea (Pisum sativum) plants was studied. Confocal laser scanning microscopy analysis of pea leaf sections with the fluorescent probe 4,5-diaminofluorescein diacetate revealed that endogenous NO. was mainly present in vascular tissues (xylem and phloem). Green fluorescence spots were also detected in the epidermal cells, palisade and spongy mesophyll cells, and guard cells. In senescent leaves, NO. generation was clearly reduced in the vascular tissues. At the subcellular level, by electron paramagnetic resonance spectroscopy with the spin trap Fe(MGD)(2) and fluorometric analysis with 4,5-diaminofluorescein diacetate, NO. was found to be an endogenous metabolite of peroxisomes. The characteristic three-line electron paramagnetic resonance spectrum of NO., with g = 2.05 and a(N) = 12.8 G, was detected in peroxisomes. By fluorometry, NO. was also found in these organelles, and the level measured of NO. was linearly dependent on the amount of peroxisomal protein. The enzymatic production of NO. from l-Arg (nitric oxide synthase [NOS]-like activity) was measured by ozone chemiluminiscence. The specific activity of peroxisomal NOS was 4.9 nmol NO. mg(-1) protein min(-1); was strictly dependent on NADPH, calmodulin, and BH(4); and required calcium. In senescent pea leaves, the NOS-like activity of peroxisomes was down-regulated by 72%. It is proposed that peroxisomal NO. could be involved in the process of senescence of pea leaves.
研究了内源一氧化氮(NO.)在幼嫩和衰老豌豆(Pisum sativum)植株叶片中的细胞和亚细胞定位。用荧光探针4,5-二氨基荧光素二乙酸酯对豌豆叶片切片进行共聚焦激光扫描显微镜分析,结果显示内源NO.主要存在于维管组织(木质部和韧皮部)中。在表皮细胞、栅栏和海绵叶肉细胞以及保卫细胞中也检测到绿色荧光斑点。在衰老叶片中,维管组织中的NO.生成明显减少。在亚细胞水平上,通过自旋捕获剂Fe(MGD)(2)的电子顺磁共振光谱和4,5-二氨基荧光素二乙酸酯的荧光分析,发现NO.是过氧化物酶体的一种内源性代谢产物。在过氧化物酶体中检测到了具有g = 2.05和a(N) = 12.8 G特征的NO.三线电子顺磁共振光谱。通过荧光测定法,在这些细胞器中也发现了NO.,并且测得的NO.水平与过氧化物酶体蛋白的量呈线性相关。通过臭氧化学发光法测定了由L-精氨酸产生NO.的酶活性(类似一氧化氮合酶[NOS]的活性)。过氧化物酶体NOS的比活性为4.9 nmol NO. mg(-1)蛋白min(-1);严格依赖于NADPH、钙调蛋白和BH(4);并且需要钙。在衰老的豌豆叶片中,过氧化物酶体的类似NOS的活性下调了72%。有人提出,过氧化物酶体NO.可能参与豌豆叶片的衰老过程。