CHLOROPHYLL DEGRADATION

THE OXIDATIVE BURST IN PLANT DISEASE RESISTANCE

Lamb, C. J., & Dixon, R. A. (1997) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.48.1.251 · Cited by 3,219

Algae: An Introduction to Phycology

Mann, D. G., & Jahns, H. M. (1996) · University of Groningen research database (University of Groningen / Centre for Information Technology) · Cited by 1,579

Evidence for Chilling-Induced Oxidative Stress in Maize Seedlings and a Regulatory Role for Hydrogen Peroxide.

Prasad, T. K., Anderson, M. D., Martin, B. A., & Stewart, C. R. (1994) · The Plant Cell · doi:10.1105/tpc.6.1.65 · Cited by 997

Chlorophyll Biosynthesis

von WETTSTEIN, D., Gough, S. P., & Kannangara, C. G. (1995) · The Plant Cell · doi:10.2307/3870056 · Cited by 511

THE DEGRADATION OF CHLOROPHYLL — A BIOLOGICAL ENIGMA

Hendry, G. A. F., Houghton, J. D., & Brown, S. B. (1987) · New Phytologist · doi:10.1111/j.1469-8137.1987.tb00181.x · Cited by 472

Chlorophyll metabolism in higher plants. VII. Chlorophyll degradation in senescing tobacco leaves; phenolic-dependent peroxidative degradation

Kato, M., & Shimizu, S. (1987) · Canadian Journal of Botany · doi:10.1139/b87-097 · Cited by 455

Crops that stay green1

Thomas, H., & Smart, C. M. (1993) · Annals of Applied Biology · doi:10.1111/j.1744-7348.1993.tb04086.x · Cited by 391

Movement and subcellular localization of a tobamovirus in Arabidopsis

Lartey, R. T., Ghoshroy, S., Ho, J., & Citovsky, V. (1997) · The Plant Journal · doi:10.1046/j.1365-313x.1997.00527.x · Cited by 336

Chlorophyll Breakdown in Senescent Leaves

Matile, P., Hörtensteiner, S., Thomas, H., & Kräutler, B. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.4.1403 · Cited by 317

An ABC‐transporter of Arabidopsis thaliana has both glutathione‐conjugate and chlorophyll catabolite transport activity

Tommasini, R., Vogt, E., Fromenteau, M., Hörtensteiner, S., Matile, P., Amrhein, N., & Martinoia, E. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00076.x · Cited by 286

Consistent Sets of Spectrophotometric Chlorophyll Equations for Acetone, Methanol and Ethanol Solvents

Ritchie, R. J. (2006) · Photosynthesis Research · doi:10.1007/s11120-006-9065-9 · Cited by 1,323

Biochemical bases of appearance and texture changes in fresh-cut fruit and vegetables

Toivonen, P. M. A., & Brummell, D. A. (2008) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2007.09.004 · Cited by 930

CHLOROPHYLL DEGRADATION DURING SENESCENCE

Hörtensteiner, S. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105212 · Cited by 868

The McCree-de Wit-Penning de Vries-Thornley respiration paradigms: 30 years later.

Amthor, J. (2000) · Annals of Botany · doi:10.1006/anbo.2000.1175 · Cited by 822

Chlorophyll breakdown in higher plants

Hörtensteiner, S., & Kräutler, B. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.12.007 · Cited by 797

Singlet oxygen production in photosynthesis

Krieger‐Liszkay, A. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh237 · Cited by 794

The molecular analysis of leaf senescence – a genomics approach

Buchanan‐Wollaston, V., Earl, S., Harrison, E., Mathas, E., Navabpour, S., Page, T., & Pink, D. A. C. (2002) · Plant Biotechnology Journal · doi:10.1046/j.1467-7652.2003.00004.x · Cited by 757

Universal chlorophyll equations for estimating chlorophylls a, b, c, and d and total chlorophylls in natural assemblages of photosynthetic organisms using acetone, methanol, or ethanol solvents

Ritchie, R. J. (2008) · Photosynthetica · doi:10.1007/s11099-008-0019-7 · Cited by 684

N ONPHOTOSYNTHETIC M ETABOLISM IN P LASTIDS

Neuhaus, H. E., & Emes, M. J. (2000) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.51.1.111 · Cited by 627

Pheophytin Pheophorbide Hydrolase (Pheophytinase) Is Involved in Chlorophyll Breakdown during Leaf Senescence in Arabidopsis

Schelbert, S., Aubry, S., Burla, B., Agne, B., Kessler, F., Krupinska, K., & Hörtensteiner, S. (2009) · The Plant Cell · doi:10.1105/tpc.108.064089 · Cited by 621

Why Leaves Turn Red in Autumn. The Role of Anthocyanins in Senescing Leaves of Red-Osier Dogwood

Feild, T. S., Lee, D. W., & Holbrook, N. M. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010063 · Cited by 583

Singlet oxygen production in photosystem II and related protection mechanism

Krieger‐Liszkay, A., Fufezan, C., & Trebst, A. (2008) · Photosynthesis Research · doi:10.1007/s11120-008-9349-3 · Cited by 572

The Senescence-Induced Staygreen Protein Regulates Chlorophyll Degradation

Park, S., Yu, J., Park, J., Li, J., Yoo, S., Lee, N.-Y., Lee, S., Jeong, S.-W., Seo, H. S., Koh, H., et al. (2007) · The Plant Cell · doi:10.1105/tpc.106.044891 · Cited by 566

Biogenesis, molecular regulation and function of plant isoprenoids.

Bouvier, F., Rahier, A., & Camara, B. (2005) · Progress in Lipid Research · doi:10.1016/j.plipres.2005.09.003 · Cited by 498

Delayed senescence of apple leaves by exogenous melatonin treatment: toward regulating the ascorbate–glutathione cycle

Wang, P., Yin, L., Liang, D., Li, C., Ma, F., & Yue, Z. (2011) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2011.00966.x · Cited by 464

Chlorophyll breakdown: Pheophorbide a oxygenase is a Rieske-type iron–sulfur protein, encoded by the accelerated cell death 1 gene

Pružinská, A., Tanner, G., Anders, I., Roca, M., & Hörtensteiner, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2036571100 · Cited by 457

Jasmonates and octadecanoids: Signals in plant stress responses and development

Wasternack, C. H., & Hause, B. (2002) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(02)72070-9 · Cited by 415

Stay-green regulates chlorophyll and chlorophyll-binding protein degradation during senescence

Hörtensteiner, S. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2009.01.002 · Cited by 413

Recent advances in chlorophyll biosynthesis and breakdown in higher plants

Eckhardt, U., Grimm, B., & H�rtensteiner, S. (2004) · Plant Molecular Biology · doi:10.1007/s11103-004-2331-3 · Cited by 384

STAY-GREEN and Chlorophyll Catabolic Enzymes Interact at Light-Harvesting Complex II for Chlorophyll Detoxification during Leaf Senescence in Arabidopsis

Sakuraba, Y., Schelbert, S., Park, S., Han, S.-H., Lee, B., Besagni, C., Kessler, F., Hörtensteiner, S., & Paek, N. (2012) · The Plant Cell · doi:10.1105/tpc.111.089474 · Cited by 372

Leaf senescence and nutrient remobilisation in barley and wheat

Gregersen, P. L., Holm, P. B., & Krupinska, K. (2008) · Plant Biology · doi:10.1111/j.1438-8677.2008.00114.x · Cited by 354

Leaf Senescence: Signals, Execution, and Regulation

Guo, Y., & Gan, S. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)71003-6 · Cited by 348

Cloning of chlorophyllase, the key enzyme in chlorophyll degradation: Finding of a lipase motif and the induction by methyl jasmonate

Tsuchiya, T., Ohta, H., Okawa, K., Iwamatsu, A., Shimada, H., Masuda, T., & Takamiya, K.-I. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.15362 · Cited by 335

An evaluation of the efficacy of using selected solvents for the extraction of lipids from algal biomass by the soxhlet extraction method

Ramluckan, K., Moodley, K. G., & Bux, F. (2013) · Fuel · doi:10.1016/j.fuel.2013.07.118 · Cited by 321

The Control of Autumn Senescence in European Aspen

Fracheboud, Y., Luquez, V., Björkén, L., Sjödin, A., Tuominen, H., & Jansson, S. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.133249 · Cited by 314

UV-C treatment delays postharvest senescence in broccoli florets

Costa, L., Vicente, A. R., Civello, P. M., CHAVES, A. R., & Martínez, G. A. (2006) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2005.10.012 · Cited by 312

Chlorophyll Breakdown in Senescent Arabidopsis Leaves. Characterization of Chlorophyll Catabolites and of Chlorophyll Catabolic Enzymes Involved in the Degreening Reaction

Pružinská, A., Tanner, G., Aubry, S., Anders, I., Moser, S., Müller, T., Ongania, K. ‐., Kräutler, B., Ji-Young, Y., Liljegren, S. J., et al. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.065870 · Cited by 309

The Arabidopsis- accelerated cell death gene ACD2 encodes red chlorophyll catabolite reductase and suppresses the spread of disease symptoms

Mach, J., Castillo, A., Hoogstraten, R. A., & Greenberg, J. T. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.771 · Cited by 306

Chlorophyll breakdown by chlorophyllase: isolation and functional expression of the Chlase1 gene from ethylene‐treated Citrus fruit and its regulation during development

Jacob‐Wilk, D., Holland, D., Goldschmidt, E. Ε., Riov, J., & Eyal, Y. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00637.x · Cited by 285

Quality-Related Enzymes in Fruit and Vegetable Products: Effects of Novel Food Processing Technologies, Part 1: High-Pressure Processing

Terefe, N. S., Buckow, R., & Versteeg, C. (2013) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2011.566946 · Cited by 281

Chlorophyllase 1, a Damage Control Enzyme, Affects the Balance between Defense Pathways in Plants

Kariola, T., Brader, G., Li, J., & Palva, E. T. (2004) · The Plant Cell · doi:10.1105/tpc.104.025817 · Cited by 277

Non-destructive tests on the prediction of apple fruit flesh firmness and soluble solids content on tree and in shelf life

Zude-Sasse, M., Heröld, B., Roger, J., Maurel, V. B., & Landahl, S. (2005) · Journal of Food Engineering · doi:10.1016/j.jfoodeng.2005.06.027 · Cited by 275

Degradation pathway(s) of chlorophyll: what has gene cloning revealed?

Takamiya, K.-I., Tsuchiya, T., & Ohta, H. (2000) · Trends in Plant Science · doi:10.1016/s1360-1385(00)01735-0 · Cited by 271

The mitochondrion – an organelle commonly involved in programmed cell death in Arabidopsis thaliana

Yao, N., Eisfelder, B. J., Marvin, J., & Greenberg, J. T. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02239.x · Cited by 269

Pigment dynamics and autumn leaf senescence in a New England deciduous forest, eastern USA

Lee, D. W., O'Keefe, J. F., Holbrook, N. M., & Feild, T. S. (2003) · Ecological Research · doi:10.1111/j.1440-1703.2003.00588.x · Cited by 262

Molecular cloning and function analysis of the stay green gene in rice

Jiang, H., Li, M., Liang, N., Yan, H., Wei, Y., Xu, X., Liu, J., Xu, Z., Chen, F., & Wu, G. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03221.x · Cited by 259

Multi-walled carbon nanotubes stimulate callus induction, secondary metabolites biosynthesis and antioxidant capacity in medicinal plant Satureja khuzestanica grown in vitro

Ghorbanpour, M., & Hadian, J. (2015) · Carbon · doi:10.1016/j.carbon.2015.07.056 · Cited by 253

Update on the biochemistry of chlorophyll breakdown

Hörtensteiner, S. (2012) · Plant Molecular Biology · doi:10.1007/s11103-012-9940-z · Cited by 249

Chlorophyllase Is a Rate-Limiting Enzyme in Chlorophyll Catabolism and Is Posttranslationally Regulated

Harpaz‐Saad, S., Azoulay, T., Arazi, T., Ben-Yaakov, E., Mett, A., Shiboleth, Y. M., Hörtensteiner, S., Gidoni, D., Gal‐On, A., Goldschmidt, E. Ε., et al. (2007) · The Plant Cell · doi:10.1105/tpc.107.050633 · Cited by 248

The Critical Role of Arabidopsis Electron-Transfer Flavoprotein:Ubiquinone Oxidoreductase during Dark-Induced Starvation

Ishizaki, K., Larson, T. R., Schauer, N., Fernie, A. R., Graham, I. A., & Leaver, C. J. (2005) · The Plant Cell · doi:10.1105/tpc.105.035162 · Cited by 244

A NAP-AAO3 Regulatory Module Promotes Chlorophyll Degradation via ABA Biosynthesis in Arabidopsis Leaves

Yang, J., Worley, E., & Udvardi, M. K. (2014) · The Plant Cell · doi:10.1105/tpc.114.133769 · Cited by 244

In Vivo Participation of Red Chlorophyll Catabolite Reductase in Chlorophyll Breakdown

Pružinská, A., Anders, I., Aubry, S., Schenk, N., Tapernoux-Lüthi, E. M., Müller, T., Kräutler, B., & Hörtensteiner, S. (2007) · The Plant Cell · doi:10.1105/tpc.106.044404 · Cited by 243

Why some leaves are anthocyanic and why most anthocyanic leaves are red?

Manetas, Y. (2005) · Flora · doi:10.1016/j.flora.2005.06.010 · Cited by 239

ArabidopsisACCELERATED CELL DEATH2 Modulates Programmed Cell Death

Yao, N., & Greenberg, J. T. (2005) · The Plant Cell · doi:10.1105/tpc.105.036251 · Cited by 239

Functional Genomic Analysis of the HY2 Family of Ferredoxin-Dependent Bilin Reductases from Oxygenic Photosynthetic Organisms

Frankenberg‐Dinkel, N., Mukougawa, K., Kohchi, T., & Lagarias, J. C. (2001) · The Plant Cell · doi:10.1105/tpc.13.4.965 · Cited by 238

Chloroplast Proteomics and the Compartmentation of Plastidial Isoprenoid Biosynthetic Pathways

Joyard, J., Ferro, M., Masselon, C., Seigneurin‐Berny, D., Salvi, D., Garin, J., & Rolland, N. (2009) · Molecular Plant · doi:10.1093/mp/ssp088 · Cited by 238

Methyl jasmonate treatments reduce chilling injury and activate the defense response of guava fruits

González-Aguilar, G. A., Tiznado‐Hernández, M. E., Zavaleta-Gatica, R., & Martínez‐Téllez, M. Á. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.11.165 · Cited by 222

Biochemistry of Indian summer: physiology of autumnal leaf coloration

Matile, P. (2000) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00081-4 · Cited by 207

TheArabidopsis vitamin E pathway gene5-1Mutant Reveals a Critical Role for Phytol Kinase in Seed Tocopherol Biosynthesis

Valentin, H. E., Lincoln, K., Moshiri, F., Jensen, P. K., Qi, Q., Venkatesh, T. V., Karunanandaa, B., Baszis, S. R., Norris, S. R., Savidge, B., et al. (2005) · The Plant Cell · doi:10.1105/tpc.105.037077 · Cited by 202

The Role of Homogentisate Phytyltransferase and Other Tocopherol Pathway Enzymes in the Regulation of Tocopherol Synthesis during Abiotic Stress

Collakova, E., & DellaPenna, D. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.026138 · Cited by 201

Transport Processes of Solutes across the Vacuolar Membrane of Higher Plants

Martinoia, E., Massonneau, A., & Frangne, N. (2000) · Plant and Cell Physiology · doi:10.1093/pcp/pcd059 · Cited by 197

The NAC transcription factor ANAC046 is a positive regulator of chlorophyll degradation and senescence in Arabidopsis leaves

Oda-Yamamizo, C., Mitsuda, N., Sakamoto, S., Ogawa, D., Ohme‐Takagi, M., & Ohmiya, A. (2016) · Scientific Reports · doi:10.1038/srep23609 · Cited by 191

Differential effects of glyphosate and aminomethylphosphonic acid (AMPA) on photosynthesis and chlorophyll metabolism in willow plants

Gomes, M. P., Manac’h, S. G. L., Maccario, S., Labrecque, M., Lucotte, M. M., & Juneau, P. (2015) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2015.11.010 · Cited by 195

Breakdown of chlorophyll: A nonenzymatic reaction accounts for the formation of the colorless “nonfluorescent” chlorophyll catabolites

Oberhuber, M., Berghold, J., Breuker, K., Hörtensteiner, S., & Kräutler, B. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1232207100 · Cited by 175

Responses of Horticultural Commodities to Low Oxygen: Limits to the Expanded Use of Modified Atmosphere Packaging

Beaudry, R. M. (2000) · HortTechnology · doi:10.21273/horttech.10.3.491 · Cited by 174

Responses of Nannochloropsis oceanica IMET1 to Long-Term Nitrogen Starvation and Recovery

Dong, H.-P., Williams, E., Wang, D.-Z., Xie, Z.-X., Hsia, R.-C., Jenck, A., Halden, R., Li, J., Chen, F., & Place, A. R. (2013) · Plant Physiology · doi:10.1104/pp.113.214320 · Cited by 173

The Cut Flower: Postharvest Considerations

da ., J. A. T. (2003) · Journal of Biological Sciences · doi:10.3923/jbs.2003.406.442 · Cited by 173

The adaptive significance of autumn leaf colours

Wilkinson, D. M., Sherratt, T. N., Phillip, D. M., Wratten, S. D., Dixon, A. F. G., & Young, A. J. (2002) · Oikos · doi:10.1034/j.1600-0706.2002.990223.x · Cited by 167

The role of plastoglobules in thylakoid lipid remodeling during plant development

Rottet, S., Besagni, C., & Kessler, F. (2015) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2015.02.002 · Cited by 168

Mechanism and Significance of Chlorophyll Breakdown

Christ, B., & Hörtensteiner, S. (2013) · Journal of Plant Growth Regulation · doi:10.1007/s00344-013-9392-y · Cited by 158

Effect of ethephon and 6-benzylaminopurine on chlorophyll degrading enzymes and a peroxidase-linked chlorophyll bleaching during post-harvest senescence of broccoli (Brassica oleracea L.) at 20°C

Costa, L., Civello, P. M., CHAVES, A. R., & Martínez, G. A. (2004) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2004.07.007 · Cited by 157

The Arabidopsis-accelerated cell death Gene ACD1 is Involved in Oxygenation of Pheophorbide a: Inhibition of the Pheophorbide a Oxygenase Activity does not Lead to the “Stay-Green” Phenotype in Arabidopsis

Tanaka, R., Hirashima, M., Satoh, S., & Tanaka, A. (2003) · Plant and Cell Physiology · doi:10.1093/pcp/pcg172 · Cited by 155

Disruption of microalgal cells using high-frequency focused ultrasound

Wang, M., Yuan, W. W., Jiang, X., Jing, Y., & Wang, Z. (2013) · Bioresource Technology · doi:10.1016/j.biortech.2013.11.054 · Cited by 159

Cytosolic pyruvate,orthophosphate dikinase functions in nitrogen remobilization during leaf senescence and limits individual seed growth and nitrogen content

Taylor, L. E., Nunes‐Nesi, A., Parsley, K., Leiss, A., Leach, G., Coates, S. A., Wingler, A., Fernie, A. R., & Hibberd, J. M. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04179.x · Cited by 150

Arabidopsis onset of leaf death mutants identify a regulatory pathway controlling leaf senescence

Jing, H., Sturre, M. J. G., Hille, J., & Dijkwel, P. P. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01400.x · Cited by 148

Effects of heat treatment on chlorophyll degrading enzymes in stored broccoli (Brassica oleracea L.)

Funamoto, Y., Yamauchi, N., Shigenaga, T., & Shigyo, M. (2002) · Postharvest Biology and Technology · doi:10.1016/s0925-5214(01)00135-1 · Cited by 147

Singlet Oxygen Stress in Microorganisms

Glaeser, J., Nuss, A. M., Berghoff, B. A., & Klug, G. (2011) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-381043-4.00004-0 · Cited by 146

Chlorophylls: Chemistry and Biological Functions

Pareek, S., Sagar, N. A., Sharma, S., Kumar, V., Agarwal, T., González-Aguilar, G. A., & Yahia, E. M. (2017) · Wiley eBooks · doi:10.1002/9781119158042.ch14 · Cited by 145

Leaf senescence and activities of the antioxidant enzymes

Procházková, D., & Wilhelmová, N. (2007) · Biologia Plantarum · doi:10.1007/s10535-007-0088-7 · Cited by 143

Coronatine alleviates salinity stress in cotton by improving the antioxidative defense system and radical-scavenging activity

Xie, Z., Duan, L., Tian, X., Wang, B., Eneji, A. E., & Li, Z. (2007) · Journal of Plant Physiology · doi:10.1016/j.jplph.2007.06.001 · Cited by 143

Chlorophyll loss associated with heat-induced senescence in bentgrass

Jespersen, D., Zhang, J., & Huang, B. (2016) · Plant Science · doi:10.1016/j.plantsci.2016.04.016 · Cited by 140

Citrus Chlorophyllase Dynamics at Ethylene-Induced Fruit Color-Break: A Study of Chlorophyllase Expression, Posttranslational Processing Kinetics, and in Situ Intracellular Localization

Azoulay‐Shemer, T., Harpaz‐Saad, S., Belausov, E., Lovat, N. E. J., Krokhin, O. V., Spicer, V., Standing, K. G., Goldschmidt, E. Ε., & Eyal, Y. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.124933 · Cited by 140

An approach to non-destructive apple fruit chlorophyll determination

Zude-Sasse, M., Truppel, I., & Heröld, B. (2002) · Postharvest Biology and Technology · doi:10.1016/s0925-5214(01)00173-9 · Cited by 139

Impact of UV-B irradiation on chlorophyll degradation and chlorophyll-degrading enzyme activities in stored broccoli (Brassica oleracea L. Italica Group) florets

Aiamla-or, S., Kaewsuksaeng, S., Shigyo, M., & Yamauchi, N. (2009) · Food Chemistry · doi:10.1016/j.foodchem.2009.10.056 · Cited by 134

Identification and fine mapping of a thermo-sensitive chlorophyll deficient mutant in rice (Oryza sativa L.)

Liu, W., Fu, Y., Hu, G., Si, H., Zhu, L., Wu, C., & Sun, Z. (2007) · Planta · doi:10.1007/s00425-007-0525-z · Cited by 133

Colorless Tetrapyrrolic Chlorophyll Catabolites Found in Ripening Fruit Are Effective Antioxidants

Müller, T., Ulrich, M., Ongania, K., & Kräutler, B. (2007) · Angewandte Chemie · doi:10.1002/anie.200703587 · Cited by 112

Effects of 1-MCP on chlorophyll degradation pathway-associated genes expression and chloroplast ultrastructure during the peel yellowing of Chinese pear fruits in storage

Cheng, Y., Dong, Y., Yan, H., Wenya, G., Shen, C., Guan, J., Liu, L., & Zhang, Y. (2012) · Food Chemistry · doi:10.1016/j.foodchem.2012.05.017 · Cited by 130

The Colors of Autumn Leaves as Symptoms of Cellular Recycling and Defenses Against Environmental Stresses

Ougham, H., Morris, P., & Thomas, H. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)66004-8 · Cited by 127

Phylogenetic and Ontogenetic Influences on the Distribution of Anthocyanins and Betacyanins in Leaves of Tropical Plants

Lee, D. W., & Collins, T. M. (2001) · International Journal of Plant Sciences · doi:10.1086/321926 · Cited by 127

Breakdown of Chlorophyll in Higher Plants—Phyllobilins as Abundant, Yet Hardly Visible Signs of Ripening, Senescence, and Cell Death

Kräutler, B. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201508928 · Cited by 129

Regulation of the tetrapyrrole biosynthetic pathway leading to heme and chlorophyll in plants and cyanobacteria

Vavilin, D. V., & Vermaas, W. F. J. (2002) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2002.1150102.x · Cited by 123

Chloroplast to chromoplast transition in tomato fruit: spectral confocal microscopy analyses of carotenoids and chlorophylls in isolated plastids and time-lapse recording on intact live tissue

Egea, I., Bian, W.-P., Barsan, C. I., Jauneau, A., Pech, J., Latché, A., Li, Z., & Christian Chervin, A. (2011) · Annals of Botany · doi:10.1093/aob/mcr140 · Cited by 120

The control of chlorophyll catabolism and the status of yellowing as a biomarker of leaf senescence

Ougham, H., Hörtensteiner, S., Armstead, I. P., Donnison, I. S., King, I. P., Thomas, H., & Mur, L. A. J. (2008) · Plant Biology · doi:10.1111/j.1438-8677.2008.00081.x · Cited by 119

Enhanced stability of thylakoid membrane proteins and antioxidant competence contribute to drought stress resistance in the tasg1 wheat stay-green mutant

Tian, F., Gong, J., Zhang, J., Zhang, M., Wang, G., Li, A.-X., & Wang, W. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert004 · Cited by 118

Phytohormones and microRNAs as sensors and regulators of leaf senescence: Assigning macro roles to small molecules

Sarwat, M., Naqvi, A. R., Ahmad, P., Ashraf, M., & Akram, N. A. (2013) · Biotechnology Advances · doi:10.1016/j.biotechadv.2013.02.003 · Cited by 118

Different Mechanisms Are Responsible for Chlorophyll Dephytylation during Fruit Ripening and Leaf Senescence in Tomato

Guyer, L., Hofstetter, S. S., Christ, B., Lira, B. S., Rossi, M., & Hörtensteiner, S. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.239541 · Cited by 117

Solar Fuel Production Based on the Artificial Photosynthesis System

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