Pheophytinase Knockdown Impacts Carbon Metabolism and Nutraceutical Content Under Normal Growth Conditions in Tomato.

Although chlorophyll (Chl) degradation is an essential biochemical pathway for plant physiology, our knowledge regarding this process still has unfilled gaps. Pheophytinase (PPH) was shown to be essential for Chl breakdown in dark-induced senescent leaves. However, the catalyzing enzymes involved in pigment turnover and fruit ripening-associated degreening are still controversial. Chl metabolism is closely linked to the biosynthesis of other isoprenoid-derived compounds, such as carotenoids and tocopherols, which are also components of the photosynthetic machinery. Chls, carotenoids and tocopherols share a common precursor, geranylgeranyl diphosphate, produced by the plastidial methylerythritol 4-phosphate (MEP) pathway. Additionally, the Chl degradation-derived phytol can be incorporated into tocopherol biosynthesis. In this context, tomato turns out to be an interesting model to address isoprenoid-metabolic cross-talk since fruit ripening combines degreening and an intensely active MEP leading to carotenoid accumulation. Here, we investigate the impact of PPH deficiency beyond senescence by the comprehensive phenotyping of SlPPH-knockdown tomato plants. In leaves, photosynthetic parameters indicate altered energy usage of excited Chl. As a mitigatory effect, photosynthesis-associated carotenoids increased while tocopherol content remained constant. Additionally, starch and soluble sugar profiles revealed a distinct pattern of carbon allocation in leaves that suggests enhanced sucrose exportation. The higher levels of carbohydrates in sink organs down-regulated carotenoid biosynthesis. Additionally, the reduction in Chl-derived phytol recycling resulted in decreased tocopherol content in transgenic ripe fruits. Summing up, tocopherol and carotenoid metabolism, together with the antioxidant capacity of the hydrophilic and hydrophobic fractions, were differentially affected in leaves and fruits of the transgenic plants. Thus, in tomato, PPH plays a role beyond senescence-associated Chl degradation that, when compromised, affects isoprenoid and carbon metabolism which ultimately alters the fruit's nutraceutical content.

[1]  F. Carrari,et al.  Down-regulation of tomato PHYTOL KINASE strongly impairs tocopherol biosynthesis and affects prenyllipid metabolism in an organ-specific manner , 2015, Journal of experimental botany.

[2]  A. Weber,et al.  Remobilization of Phytol from Chlorophyll Degradation Is Essential for Tocopherol Synthesis and Growth of Arabidopsis , 2015, Plant Cell.

[3]  E. Cahoon,et al.  Chlorophyll Synthase under Epigenetic Surveillance Is Critical for Vitamin E Synthesis, and Altered Expression Affects Tocopherol Levels in Arabidopsis1[OPEN] , 2015, Plant Physiology.

[4]  F. Carrari,et al.  Crop yield: challenges from a metabolic perspective. , 2015, Current opinion in plant biology.

[5]  F. Carrari,et al.  Fruits from ripening impaired, chlorophyll degraded and jasmonate insensitive tomato mutants have altered tocopherol content and composition. , 2015, Phytochemistry.

[6]  Y. Charng,et al.  Analysis of an Arabidopsis heat-sensitive mutant reveals that chlorophyll synthase is involved in reutilization of chlorophyllide during chlorophyll turnover. , 2014, The Plant journal : for cell and molecular biology.

[7]  L. Freschi,et al.  Plant degreening: evolution and expression of tomato (Solanum lycopersicum) dephytylation enzymes. , 2014, Gene.

[8]  So-Yon Park,et al.  Arabidopsis STAY-GREEN2 is a negative regulator of chlorophyll degradation during leaf senescence. , 2014, Molecular plant.

[9]  E. Cahoon,et al.  Chlorophyll Degradation: The Tocopherol Biosynthesis-Related Phytol Hydrolase in Arabidopsis Seeds Is Still Missing1[C][W][OPEN] , 2014, Plant Physiology.

[10]  Bruno S. Lira,et al.  Different Mechanisms Are Responsible for Chlorophyll Dephytylation during Fruit Ripening and Leaf Senescence in Tomato1[W][OPEN] , 2014, Plant Physiology.

[11]  H. Thomas,et al.  The stay-green trait. , 2014, Journal of experimental botany.

[12]  D. Centeno,et al.  Leaf metabolite profile of the Brazilian resurrection plant Barbacenia purpurea Hook. (Velloziaceae) shows two time-dependent responses during desiccation and recovering , 2014, Front. Plant Sci..

[13]  L. P. Bidel,et al.  Carotenoid responses to environmental stimuli: integrating redox and carbon controls into a fruit model. , 2014, Plant, cell & environment.

[14]  Koichiro Tamura,et al.  MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. , 2013, Molecular biology and evolution.

[15]  E. Fantini,et al.  Dissection of Tomato Lycopene Biosynthesis through Virus-Induced Gene Silencing1[C][W][OPEN] , 2013, Plant Physiology.

[16]  S. Hörtensteiner Update on the biochemistry of chlorophyll breakdown , 2013, Plant Molecular Biology.

[17]  J. Giovannoni,et al.  A STAY-GREEN protein SlSGR1 regulates lycopene and β-carotene accumulation by interacting directly with SlPSY1 during ripening processes in tomato. , 2013, The New phytologist.

[18]  J. Rose,et al.  Regulation of ripening and opportunities for control in tomato and other fruits. , 2013, Plant biotechnology journal.

[19]  T. Duffy,et al.  Transcriptional regulation of tocopherol biosynthesis in tomato , 2013, Plant Molecular Biology.

[20]  M. Qi,et al.  Photosynthesis, photoinhibition, and antioxidant system in tomato leaves stressed by low night temperature and their subsequent recovery. , 2012, Plant science : an international journal of experimental plant biology.

[21]  J. Pech,et al.  Proteomic Analysis of Chloroplast-to-Chromoplast Transition in Tomato Reveals Metabolic Shifts Coupled with Disrupted Thylakoid Biogenesis Machinery and Elevated Energy-Production Components1[W] , 2012, Plant Physiology.

[22]  Daniel W. A. Buchan,et al.  The tomato genome sequence provides insights into fleshy fruit evolution , 2012, Nature.

[23]  Su-Hyun Han,et al.  STAY-GREEN and Chlorophyll Catabolic Enzymes Interact at Light-Harvesting Complex II for Chlorophyll Detoxification during Leaf Senescence in Arabidopsis[C][W] , 2012, Plant Cell.

[24]  David M. Goodstein,et al.  Phytozome: a comparative platform for green plant genomics , 2011, Nucleic Acids Res..

[25]  Zhengguo Li,et al.  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. , 2011, Annals of botany.

[26]  R. Tanaka,et al.  Chlorophyll cycle regulates the construction and destruction of the light-harvesting complexes. , 2011, Biochimica et biophysica acta.

[27]  F. Carrari,et al.  Genetic dissection of vitamin E biosynthesis in tomato , 2011, Journal of experimental botany.

[28]  Christian Wilhelm,et al.  Energy dissipation is an essential mechanism to sustain the viability of plants: The physiological limits of improved photosynthesis. , 2011, Journal of plant physiology.

[29]  L. Freschi,et al.  Correlation between citric acid and nitrate metabolisms during CAM cycle in the atmospheric bromeliad Tillandsia pohliana. , 2010, Journal of plant physiology.

[30]  S. Shigeoka,et al.  Understanding Oxidative Stress and Antioxidant Functions to Enhance Photosynthesis1 , 2010, Plant Physiology.

[31]  F. Rolland,et al.  Sugar signalling and antioxidant network connections in plant cells , 2010, The FEBS journal.

[32]  O. Gascuel,et al.  New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. , 2010, Systematic biology.

[33]  H. Gautier,et al.  HPLC assay of tomato carotenoids: validation of a rapid microextraction technique. , 2009, Journal of agricultural and food chemistry.

[34]  I. Vass,et al.  Janus-faced charge recombinations in photosystem II photoinhibition. , 2009, Trends in plant science.

[35]  B. Burla,et al.  Pheophytin Pheophorbide Hydrolase (Pheophytinase) Is Involved in Chlorophyll Breakdown during Leaf Senescence in Arabidopsis[W][OA] , 2009, The Plant Cell Online.

[36]  A. Moorman,et al.  Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data , 2009, Nucleic acids research.

[37]  P. Gallusci,et al.  Effects of exogenous glucose on carotenoid accumulation in tomato leaves. , 2008, Physiologia plantarum.

[38]  R. Tanaka,et al.  Tetrapyrrole biosynthesis in higher plants. , 2007, Annual review of plant biology.

[39]  B. Pogson,et al.  Vitamin synthesis in plants: tocopherols and carotenoids. , 2006, Annual review of plant biology.

[40]  Junsoo Lee,et al.  Tocopherol and tocotrienol contents of raw and processed fruits and vegetables in the United States diet , 2006 .

[41]  P. Dörmann,et al.  A Salvage Pathway for Phytol Metabolism in Arabidopsis* , 2006, Journal of Biological Chemistry.

[42]  R. Last,et al.  The Arabidopsis vitamin E pathway gene5-1 Mutant Reveals a Critical Role for Phytol Kinase in Seed Tocopherol Biosynthesis[W][OA] , 2005, The Plant Cell Online.

[43]  P. Rey,et al.  Vitamin E Protects against Photoinhibition and Photooxidative Stress in Arabidopsis thaliana , 2005, The Plant Cell Online.

[44]  John W Erdman,et al.  The tomato as a functional food. , 2005, The Journal of nutrition.

[45]  P. Dörmann,et al.  Alterations in Tocopherol Cyclase Activity in Transgenic and Mutant Plants of Arabidopsis Affect Tocopherol Content, Tocopherol Composition, and Oxidative Stress1 , 2005, Plant Physiology.

[46]  G. Horgan,et al.  Relative expression software tool (REST©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR , 2002 .

[47]  W. Frommer,et al.  SUT2, a Putative Sucrose Sensor in Sieve Elements , 2000, Plant Cell.

[48]  K Maxwell,et al.  Chlorophyll fluorescence--a practical guide. , 2000, Journal of experimental botany.

[49]  H. Thomas,et al.  Five ways to stay green. , 2000, Journal of experimental botany.

[50]  C. Rice-Evans,et al.  Antioxidant activity applying an improved ABTS radical cation decolorization assay. , 1999, Free radical biology & medicine.

[51]  P. Di Mascio,et al.  Physical and chemical scavenging of singlet molecular oxygen by tocopherols. , 1990, Archives of biochemistry and biophysics.

[52]  R. J. Porra,et al.  Determination of accurate extinction coefficients and simultaneous equations for assaying chlorophylls a and b extracted with four different solvents: verification of the concentration of chlorophyll standards by atomic absorption spectroscopy , 1989 .

[53]  W. Gruissem,et al.  Changes in Photosynthetic Capacity and Photosynthetic Protein Pattern during Tomato Fruit Ripening. , 1987, Plant physiology.

[54]  A. Holzwarth,et al.  The role of the xanthophyll cycle and of lutein in photoprotection of photosystem II. , 2012, Biochimica et biophysica acta.

[55]  P. Pospíšil Molecular mechanisms of production and scavenging of reactive oxygen species by photosystem II. , 2012, Biochimica et biophysica acta.

[56]  K. Fukuzawa,et al.  Kinetics and dynamics of singlet oxygen scavenging by alpha-tocopherol in phospholipid model membranes. , 1997, Free radical biology & medicine.