1.14.15.17 evolution AtPaO is a Rieske-type iron–sulfur cluster-containing enzyme that is identical to Arabidopsis accelerated cell death 1 and homologous to lethal leaf spot 1 (LLS1) of maize 676765 1.14.15.17 evolution PaO is an evolutionarily conserved protein, and EAS1 is 68% identical to the Arabidopsis ACCERLERATED CELL DEATH (ACD1) protein -, 736578 1.14.15.17 malfunction during the early growth stage (at the 3th leaf stage), eas1 mutants do not show detectable differences compared to wild-type plants. At the heading stage, old leaves of eas1 mutants turn yellowish or brownish, when wild-type plants are still healthy and green. Small chlorotic lesions are first observed near the tip, and then spread down to the entire leaves of eas1 mutants. At the grain filling stage, the leaf senescence phenotype of eas1 is more apparent compared to wild-type, as most eas1 mutant leaves, culms and sheaths turned to dark brown. In addition to the leaf senescence phenotype, the mature eas1 mutant plants also exhibit apparent developmental defects, such as semi-dwarfism, reduced tiller number and partial-filling -, 736578 1.14.15.17 malfunction enzyme inhibition or downregulation leads to accumulation of pheophorbide a, a key intermediate of chlorophyll catabolism, which causes cell death in complete darkness in a transgenic Arabidopsis plant, As-ACD1. When senescence is induced by a continuous dark period, leaves of As-ACD1 plants become dehydrated, phenotype, overview 700721 1.14.15.17 malfunction the absence of PAO in mutants or antisense lines from different plant species results in premature cell death. Phototoxicity of Pheide a is considered to trigger the observed cell death phenotype in a light-dependent manner 737013 1.14.15.17 metabolism chlorophyll metabolism and proteins (enzymes) involved, including pheophorbide a oxygenase, overview -, 737240 1.14.15.17 metabolism enzyme PaO seems to be a key regulator of chlorophyll catabolism 676765 1.14.15.17 metabolism in land plants, chlorophyll is broken down to colorless linear tetrapyrroles in a highly conserved multistep pathway. The pathway is termed the PAO pathway, because the opening of the chlorine macrocycle present in chlorophyll catalyzed by pheophorbide a oxygenase (PAO), the key enzyme of the pathway. The PAO pathway is active during leaf senescence and in ripening fruits. Chlorophyll breakdown does not only occur during leaf senescence and fruit ripening, but also at steady state, during post-harvest and in response to biotic and abiotic stresses, chlorophyll is turned over or degraded, at least to some extent 737013 1.14.15.17 metabolism in land plants, chlorophyll is broken down to colorless linear tetrapyrroles in a highly conserved multistep pathway. The pathway is termed the PAO pathway, because the opening of the chlorophyllide macrocycle present in chlorophyll catalyzed by pheophorbide a oxygenase (PAO), the key enzyme of the pathway. The PAO pathway is active during leaf senescence and in ripening fruits. Chlorophyll breakdown does not only occur during leaf senescence and fruit ripening, but also at steady state, during post-harvest and in response to biotic and abiotic stresses, chlorophyll is turned over or degraded, at least to some extent 737013 1.14.15.17 metabolism the enzyme is important in the chlorophyll degradation pathway during leaf senescence. The porphyrin macrocycle of pheophorbide is oxygenolytically cleaved by the joint action of pheophorbide, the pheophorbide a oxygenase, PaO, and the red chlorophyll catabolite reductase, RCCR, overview 699270 1.14.15.17 additional information catabolites such as hypermodified FCCs and urobilinogenoidic chlorophyll catabolites point to divergent paths of the PAO pathway that might exist in some plant species 737013 1.14.15.17 physiological function a close correlation between chlorophyll degradation and enzyme expression exists during broccoli senescence 725808 1.14.15.17 physiological function chlorophyll breakdown during senescence is an integral part of plant development and leads to the accumulation of colorless catabolites. The loss of green pigment is due to an oxygenolytic opening of the porphyrin macrocycle of pheophorbide (pheide) a followed by a reduction to yield a fluorescent chlorophyll catabolite. This step is comprised of the interaction of two enzymes, pheide a oxygenase (PaO) and red chl catabolite reductase. Senescence-related activity of PaO 676765 1.14.15.17 physiological function gene EAS1 encodes a PaO enzyme containing a putative bipartite chloroplast-targeting peptide, both of which are genetically important for the function of EAS1 during plant growth and development. Pheophorbide a oxygenase (PaO) is a key enzyme for chlorophyll breakdown and involved in chlorophyll degradation during leaf senescence -, 736578 1.14.15.17 physiological function physical interaction between pheophorbide a oxygenase, PAO, and red chlorophyll catabolite reductase, RCCR, required for activity, and interaction with stay-green proteins 737013 1.14.15.17 physiological function physical interaction between pheophorbide a oxygenase, PAO, and red chlorophyll catabolite reductase, RCCR, required for activity, and interaction with stay-green proteins, the latter is required for PaO-RCCR interaction. PaO enzyme expression is highly regulated 737013