Cited by 152Plant biochemistry and biosynthesisPhotosynthetic Processes and MechanismsAlgal biology and biofuel production

The DOI matches its Crossref record; 40 of the 42 references it cites were found in a registry or an index.

Xanthophyll synthesis in diatoms: quantification of putative intermediates and comparison of pigment conversion kinetics with rate constants derived from a model

Lohr, Martin, Wilhelm, Christian·2001·Planta

DOI 10.1007/s004250000403

Open this paper in CoChat — free account

Abstract

Recently, we reported the presence of the violaxanthin-antheraxanthin-zeaxanthin cycle in diatoms, and showed that violaxanthin is the putative precursor of both diadinoxanthin and fucoxanthin in the diatom Phaeodactylum tricornutum Bohlin (M. Lohr and C. Wilhelm, 1999, Proc. Natl. Acad. Sci. USA 96: 8784-8789). In the present study, two possible intermediates in the synthesis of violaxanthin from beta-carotene were identified in P. tricornutum, namely beta-cryptoxanthin and beta-cryptoxanthin epoxide. In low light, the latter pigment prevails, but in high light beta-cryptoxanthin accumulates, probably as the result of an increased activity of the xantophyll-cycle de-epoxidase. The apparent kinetics of several xanthophyll conversion steps were determined for P. tricornutum and Cyclotella meneghiniana Kuitzing. The experimentally determined conversion rates were used to evaluate the hypothetical pathway of xanthophyll synthesis in diatoms. For this purpose a mathematical model was developed which allows the calculation of theoretical rates of pigment conversion for microalgae under steady-state growth conditions. A comparison between measured and calculated conversion rates agreed well with the proposal of a sequential synthesis of fucoxanthin via violaxanthin and diadinoxanthin. The postulation of zeaxanthin as an obligatory intermediate in the synthesis of violaxanthin, however, resulted in large discrepancies between the measured and calculated rates of its epoxidation. Instead of zeaxanthin, beta-cryptoxanthin epoxide may be involved in the biosynthesis of violaxanthin in diatoms.

Integrity signals

Registry

Crossref · 10.1007/s004250000403

Cites

40 of 40 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

PHOTOPROTECTION REVISITED:Genetic and Molecular Approaches
Niyogi, K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.333 · Cited by 1,937
GENES AND ENZYMES OF CAROTENOID BIOSYNTHESIS IN PLANTS
Cunningham, F. X., & Gantt, E. (1998) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.49.1.557 · Cited by 966
Photoinhibition and Zeaxanthin Formation in Intact Leaves
Demmig, B., Winter, K., Krüger, A., & Czygan, F. (1987) · PLANT PHYSIOLOGY · doi:10.1104/pp.84.2.218 · Cited by 769
In vivo functions of carotenoids in higher plants
Demmig‐Adams, B., Gilmore, A. M., & Adams, W. W. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.4.8647339 · Cited by 765
The light‐harvesting and protective functions of carotenoids in photosynthetic membranes
Siefermann‐Harms, D. (1987) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1987.tb09240.x · Cited by 636
Molecular identification of zeaxanthin epoxidase of Nicotiana plumbaginifolia, a gene involved in abscisic acid biosynthesis and corresponding to the ABA locus of Arabidopsis thaliana.
Marín, E., Nussaume, L., Quesada, A., Gonneau, M., Sotta, B., Hugueney, P., Frey, A., & Marion‐Poll, A. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00589.x · Cited by 550
ChemInform Abstract: UV/Visible Spectroscopy
Britton, G. (1995) · ChemInform · doi:10.1002/chin.199532313 · Cited by 461
The aba mutant of Arabidopsis thaliana is impaired in epoxy-carotenoid biosynthesis.
Rock, C. D., & Zeevaart, J. A. D. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.17.7496 · Cited by 358
Chlamydomonas Xanthophyll Cycle Mutants Identified by Video Imaging of Chlorophyll Fluorescence Quenching.
Niyogi, K. K., Bjorkman, O., & Grossman, A. R. (1997) · The Plant Cell · doi:10.1105/tpc.9.8.1369 · Cited by 326
Linear models relating xanthophylls and lumen acidity to non-photochemical fluorescence quenching. Evidence that antheraxanthin explains zeaxanthin-independent quenching
Gilmore, A. M., & Yamamoto, H. Y. (1993) · Photosynthesis Research · doi:10.1007/bf02185412 · Cited by 317

Show all 42 references

Sorted by citations

Photoprotection in plants: a new light on photosystem II damage
Takahashi, S., & Badger, M. R. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.10.001 · Cited by 1,041
In Posidonia oceanica cadmium induces changes in DNA methylation and chromatin patterning
Greco, M., Chiappetta, A. A. C., Bruno, L., & Bitonti, M. B. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err313 · Cited by 555
Photosynthetic pigments in diatoms
Kuczynska, P., Jemiola-Rzeminska, M., & Strzalka, K. (2015) · Marine Drugs · doi:10.3390/md13095847 · Cited by 428
Regulation and function of xanthophyll cycle-dependent photoprotection in algae
Goss, R., & Jakob, T. (2010) · Photosynthesis Research · doi:10.1007/s11120-010-9536-x · Cited by 429
The Regulation of Carbon and Nutrient Assimilation in Diatoms is Significantly Different from Green Algae
Wilhelm, C., Büchel, C., Fisahn, J., Goss, R., Jakob, T., LaRoche, J., Lavaud, J., Lohr, M., Riebesell, U., Stehfest, K., et al. (2006) · Protist · doi:10.1016/j.protis.2006.02.003 · Cited by 320
Phototrophic pigment production with microalgae: biological constraints and opportunities
Mulders, K. J. M., Lamers, P. P., Martens, D. E., & Wijffels, R. H. (2014) · Journal of Phycology · doi:10.1111/jpy.12173 · Cited by 302
The Potential of Seaweeds as a Source of Functional Ingredients of Prebiotic and Antioxidant Value
Gomez-Zavaglia, A., Prieto Lage, M. A., Jimenez-Lopez, C., Mejuto, J. C., & Simal-Gandara, J. (2019) · Antioxidants · doi:10.3390/antiox8090406 · Cited by 280
An Integrated Analysis of Molecular Acclimation to High Light in the Marine Diatom Phaeodactylum tricornutum
Nymark, M., Valle, K. C., Brembu, T., Hancke, K., Winge, P., Andresen, K., Johnsen, G. H., & Bones, A. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007743 · Cited by 293
EVALUATION OF RECOVERABLE FUNCTIONAL LIPID COMPONENTS OF SEVERAL BROWN SEAWEEDS (PHAEOPHYTA) FROM JAPAN WITH SPECIAL REFERENCE TO FUCOXANTHIN AND FUCOSTEROL CONTENTS1
Terasaki, M., Hirose, A., Narayan, B., Baba, Y., Kawagoe, C., Yasui, H., Saga, N., Hosokawa, M., & Miyashita, K. (2009) · Journal of Phycology · doi:10.1111/j.1529-8817.2009.00706.x · Cited by 184
Evidence for the Existence of One Antenna-Associated, Lipid-Dissolved and Two Protein-Bound Pools of Diadinoxanthin Cycle Pigments in Diatoms
Bernard, L., Volke, D., Gilbert, M., Wilhelm, C., & Goss, R. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.166454 · Cited by 174
Valuable pigments from microalgae: phycobiliproteins, primary carotenoids, and fucoxanthin
Zittelli, G. C., Lauceri, R., Faraloni, C., Benavides, A. M. S., & Torzillo, G. (2023) · Photochemical & Photobiological Sciences · doi:10.1007/s43630-023-00407-3 · Cited by 192
Carotenoid biosynthesis in diatoms
Bertrand, M. (2010) · Photosynthesis Research · doi:10.1007/s11120-010-9589-x · Cited by 182
The importance of a highly active and ΔpH-regulated diatoxanthin epoxidase for the regulation of the PS II antenna function in diadinoxanthin cycle containing algae
Goss, R., Pinto, E. A., Wilhelm, C., & Richter, M. (2005) · Journal of Plant Physiology · doi:10.1016/j.jplph.2005.09.008 · Cited by 172
Anti-Inflammatory and Anticancer Effects of Microalgal Carotenoids
Ávila‐Román, J., García-Gil, S., Rodríguez-Luna, A., Motilva, V., & Talero, E. (2021) · Marine Drugs · doi:10.3390/md19100531 · Cited by 175
GROWTH INHIBITION AND TOXICITY OF THE DIATOM ALDEHYDE 2‐TRANS, 4‐TRANS‐DECADIENAL ON THALASSIOSIRA WEISSFLOGII (BACILLARIOPHYCEAE)1
Casotti, R., Mazza, S., Brunet, C., Vantrepotte, V., Ianora, A., & Miralto, A. (2005) · Journal of Phycology · doi:10.1111/j.1529-8817.2005.04052.x · Cited by 165
Evolutionary Origins and Functions of the Carotenoid Biosynthetic Pathway in Marine Diatoms
Coesel, S., Obornı́k, M., Varela, J. C. S., Falciatore, A., & Bowler, C. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002896 · Cited by 163
Ultrafast fluorescence study on the location and mechanism of non-photochemical quenching in diatoms
Miloslavina, Y., Grouneva, I., Lambrev, P. H., Bernard, L., Goss, R., Wilhelm, C., & Holzwarth, A. R. (2009) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2009.05.012 · Cited by 151
Ancient Recruitment by Chromists of Green Algal Genes Encoding Enzymes for Carotenoid Biosynthesis
Frommolt, R., Werner, S., Paulsen, H., Goss, R., Wilhelm, C., Zauner, S., Maier, U., Grossman, A. R., Bhattacharya, D., & Lohr, M. (2008) · Molecular Biology and Evolution · doi:10.1093/molbev/msn206 · Cited by 141
Pigments and photoacclimation processes
Brunet, C., Johnsen, G. H., Lavaud, J., & Roy, S. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511732263.017 · Cited by 133
Biosynthesis of fucoxanthin and diadinoxanthin and function of initial pathway genes in Phaeodactylum tricornutum
Dambek, M., Eilers, U., Breitenbach, J., Steiger, S., Büchel, C., & Sandmann, G. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers211 · Cited by 132
New insights on the dominance of cryptophytes in Antarctic coastal waters: A case study in Gerlache Strait
Mendes, C. R. B., Tavano, V. M., Dotto, T. S., Kerr, R., de Souza, M. S., Garcia, C. A. E., & Secchi, E. R. (2017) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2017.02.010 · Cited by 128
Spectroscopic and Molecular Characterization of the Oligomeric Antenna of the DiatomPhaeodactylum tricornutum
Bernard, L., Volke, D., Szabó, M., Hoffmann, R., Garab, G., Wilhelm, C., & Goss, R. (2007) · Biochemistry · doi:10.1021/bi7008344 · Cited by 128
Diatoms as cell factories for high-value products: chrysolaminarin, eicosapentaenoic acid, and fucoxanthin
Yang, R., Wei, D., & Xie, J. (2020) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2020.1805402 · Cited by 125
Mathematical Modeling of Plant Metabolic Pathways
Morgan, J. A., & Rhodes, D. (2002) · Metabolic Engineering · doi:10.1006/mben.2001.0211 · Cited by 116
Carotenoids in Microalgae
Henríquez, V., Escobar, C., Galarza, J. I., & Gimpel, J. A. (2016) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-319-39126-7_8 · Cited by 112
Fast Regulation of Photosynthesis in Diatoms: Mechanisms, Evolution and Ecophysiology
Lavaud, J. (2007) · HAL · Cited by 109
Green diatom mutants reveal an intricate biosynthetic pathway of fucoxanthin
Bai, Y. J., Cao, T., Dautermann, O., Buschbeck, P., Cantrell, M., Chen, Y., Lein, C. D., Shi, X., Ware, M. A., Yang, F., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2203708119 · Cited by 110
Improving Fucoxanthin Production in Mixotrophic Culture of Marine Diatom Phaeodactylum tricornutum by LED Light Shift and Nitrogen Supplementation
Yang, R., & Wei, D. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00820 · Cited by 106
Unlocking the health potential of microalgae as sustainable sources of bioactive compounds
Saide, A., Martínez, K. A., Ianora, A., & Lauritano, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094383 · Cited by 105
A review on the progress, challenges and prospects in commercializing microalgal fucoxanthin
Wang, S., Wu, S. S., Yang, G., Pan, K., Wang, L., & Hu, Z. (2021) · Biotechnology Advances · doi:10.1016/j.biotechadv.2021.107865 · Cited by 107
The regulation of xanthophyll cycle activity and of non-photochemical fluorescence quenching by two alternative electron flows in the diatoms Phaeodactylum tricornutum and Cyclotella meneghiniana
Grouneva, I., Jakob, T., Wilhelm, C., & Goss, R. (2009) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2009.02.004 · Cited by 103
Low-Molecular-Weight Metabolites from Diatoms: Structures, Biological Roles and Biosynthesis
Stonik, V. A., & Стоник, И. В. (2015) · Marine Drugs · doi:10.3390/md13063672 · Cited by 109
Fucoxanthin from Algae to Human, an Extraordinary Bioresource: Insights and Advances in up and Downstream Processes
Pajot, A., Huynh, G. H., Picot, L., Marchal, L., & Nicolau, É. (2022) · Marine Drugs · doi:10.3390/md20040222 · Cited by 107
Photoprotection and xanthophyll‐cycle activity in three marine diatoms1
Dimier, C., Corato, F., Tramontano, F., & Brunet, C. (2007) · Journal of Phycology · doi:10.1111/j.1529-8817.2007.00381.x · Cited by 97
Light acclimation in diatoms: From phenomenology to mechanisms
Wilhelm, C., Jungandreas, A., Jakob, T., & Goss, R. (2014) · Marine Genomics · doi:10.1016/j.margen.2013.12.003 · Cited by 95
Photosystem II Photoinactivation, Repair, and Protection in Marine Centric Diatoms
Wu, H., Roy, S., Alami, M., Green, B. R., & Campbell, D. A. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.203067 · Cited by 95
Photoinhibition, UV-B and Algal Photosynthesis
Franklin, L. A., Osmond, C. B., & Larkum, A. W. D. (2003) · Advances in photosynthesis and respiration · doi:10.1007/978-94-007-1038-2_16 · Cited by 96
Lipid Dependence of Xanthophyll Cycling in Higher Plants and Algae
Goss, R., & Latowski, D. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00455 · Cited by 93
Comparative Ecophysiology of the Xanthophyll Cycle in Six Marine Phytoplanktonic Species
Dimier, C., Giovanni, S., Tramontano, F., & Brunet, C. (2009) · Protist · doi:10.1016/j.protis.2009.03.001 · Cited by 89
Silencing of the Violaxanthin De-Epoxidase Gene in the Diatom Phaeodactylum tricornutum Reduces Diatoxanthin Synthesis and Non-Photochemical Quenching
Lavaud, J., Materna, A. C., Sturm, S., Vugrinec, S., & Kroth, P. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036806 · Cited by 95
An algal enzyme required for biosynthesis of the most abundant marine carotenoids
Dautermann, O., Lyska, D., Andersen‐Ranberg, J., Becker, M., Fröhlich‐Nowoisky, J., Gartmann, H., Krämer, L. C., Mayr, K., Pieper, D. H., Rij, L. M., et al. (2020) · Science Advances · doi:10.1126/sciadv.aaw9183 · Cited by 84
Bioprospecting of fucoxanthin from diatoms — Challenges and perspectives
Seth, K., Kumar, A., Rastogi, R. P., Meena, M., Vinayak, V., & Harish (2021) · Algal Research · doi:10.1016/j.algal.2021.102475 · Cited by 85
Investigation of the quenching efficiency of diatoxanthin in cells of Phaeodactylum tricornutum (Bacillariophyceae) with different pool sizes of xanthophyll cycle pigments
Schumann, A., Goss, R., Jakob, T., & Wilhelm, C. (2007) · Phycologia · doi:10.2216/06-30.1 · Cited by 80
Influence of ascorbate and pH on the activity of the diatom xanthophyll cycle‐enzyme diadinoxanthin de‐epoxidase
Grouneva, I., Jakob, T., Wilhelm, C., & Goss, R. (2006) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2006.00613.x · Cited by 79
Circadian variability in the photobiology of Phaeodactylum tricornutum: pigment content
Ragni, M., & d’Alcalà, M. R. (2007) · Journal of Plankton Research · doi:10.1093/plankt/fbm002 · Cited by 78
Community analysis of pigment patterns from 37 microalgae strains reveals new carotenoids and porphyrins characteristic of distinct strains and taxonomic groups
Serive, B., Nicolau, É., Bérard, J., Kaas, R., Pasquet, V., Picot, L., & Cadoret, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171872 · Cited by 75
A New Multicomponent NPQ Mechanism in the Diatom Cyclotella meneghiniana
Grouneva, I., Jakob, T., Wilhelm, C., & Goss, R. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn097 · Cited by 75
An assessment of cryptic genetic diversity within theCyclotella meneghinianaspecies complex (Bacillariophyta) based on nuclear and plastid genes, and amplified fragment length polymorphisms
Beszteri, B., John, U., & Medlin, L. K. (2007) · European Journal of Phycology · doi:10.1080/09670260601044068 · Cited by 69
Dynamic Changes between Two LHCX-Related Energy Quenching Sites Control Diatom Photoacclimation
Taddei, L., Chukhutsina, V. U., Bernard, L., Stella, G. R., Bassi, R., van Amerongen, H., Bouly, J., Jaubert, M. J., Finazzi, G., & Falciatore, A. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.00448 · Cited by 66
The Non-Photochemical Quenching of the Electronically Excited State of Chlorophyll a in Plants: Definitions, Timelines, Viewpoints, Open Questions
Papageorgiou, G. C., & Jee, G. (2014) · Advances in photosynthesis and respiration · doi:10.1007/978-94-017-9032-1_1 · Cited by 69
Determination of fucoxanthin isomers in microalgae ( Isochrysis sp.) by high‐performance liquid chromatography coupled with diode‐array detector multistage mass spectrometry coupled with positive electrospray ionization
Crupi, P., Toci, A. T., Mangini, S., Wrubl, F., Rodolfi, L., Tredici, M. R., Coletta, A., & Antonacci, D. (2013) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.6531 · Cited by 64
Engineering the Unicellular Alga Phaeodactylum tricornutum for Enhancing Carotenoid Production
Manfellotto, F., Stella, G. R., Falciatore, A., Brunet, C., & Ferrante, M. I. (2020) · Antioxidants · doi:10.3390/antiox9080757 · Cited by 63
Chlorophyll synthesis and the photoprotective mechanism in leaves of mulberry (Morus alba L.) seedlings under NaCl and NaHCO3 stress revealed by TMT-based proteomics analyses
Zhang, H., Yue, W., Li, X., Guoqiang, H., Yanhui, C., Zhiyuan, T., Jie-yu, S., Xu, N., & Guangyu, S. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.110164 · Cited by 61
The lipid dependence of diadinoxanthin de-epoxidation presents new evidence for a macrodomain organization of the diatom thylakoid membrane
Goss, R., Nerlich, J., Bernard, L., Schaller, S., Vieler, A., & Wilhelm, C. (2009) · Journal of Plant Physiology · doi:10.1016/j.jplph.2009.05.017 · Cited by 57
ACCLIMATION OF EMILIANIA HUXLEYI (PRYMNESIOPHYCEAE) TO PHOTON FLUX DENSITY 1
Harris, G. N., Scanlan, D. J., & Geider, R. J. (2005) · Journal of Phycology · doi:10.1111/j.1529-8817.2005.00109.x · Cited by 56
Structurally flexible macro-organization of the pigment–protein complexes of the diatom Phaeodactylum tricornutum
Szabó, M., Bernard, L., Goss, R., Wilhelm, C., Mustárdy, L., & Garab, G. (2007) · Photosynthesis Research · doi:10.1007/s11120-007-9252-3 · Cited by 55
Lipid dependence of diadinoxanthin solubilization and de-epoxidation in artificial membrane systems resembling the lipid composition of the natural thylakoid membrane
Goss, R., Latowski, D., Grzyb, J., Vieler, A., Lohr, M., Wilhelm, C., & Strzałka, K. (2006) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2006.06.006 · Cited by 55
Supplementary Ultraviolet-B Radiation Induces a Rapid Reversal of the Diadinoxanthin Cycle in the Strong Light-Exposed DiatomPhaeodactylum tricornutum
Mewes, H., & Richter, M. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.006775 · Cited by 54
A functional zeaxanthin epoxidase from red algae shedding light on the evolution of light‐harvesting carotenoids and the xanthophyll cycle in photosynthetic eukaryotes
Dautermann, O., & Lohr, M. (2017) · The Plant Journal · doi:10.1111/tpj.13725 · Cited by 54
Evolutionary origins, molecular cloning and expression of carotenoid hydroxylases in eukaryotic photosynthetic algae
Cui, H., Yu, X., Wang, Y., Cui, Y., Li, X., Liu, Z., & Qin, S. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-457 · Cited by 50
An unexpected hydratase synthesizes the green light-absorbing pigment fucoxanthin
Cao, T., Bai, Y. J., Buschbeck, P., Tan, Q., Cantrell, M., Chen, Y., Jiang, Y., Liu, R., Ries, N. K., Shi, X., et al. (2023) · The Plant Cell · doi:10.1093/plcell/koad116 · Cited by 49
Impact of chlororespiration on non-photochemical quenching of chlorophyll fluorescence and on the regulation of the diadinoxanthin cycle in the diatom Thalassiosira pseudonana
Cruz, S., Goss, R., Wilhelm, C., Leegood, R. C., Horton, P., & Jakob, T. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq284 · Cited by 50
Opportunities for the marine carotenoid value chain from the perspective of fucoxanthin degradation
Yusof, Z., Khong, N. M. H., Choo, W. S., & Foo, S. C. (2022) · Food Chemistry · doi:10.1016/j.foodchem.2022.132394 · Cited by 51
Growth and pigment accumulation in nutrient-depleted Isochrysis aff. galbana T-ISO
Mulders, K. J. M., Weesepoel, Y., Lamers, P. P., Vincken, J., Martens, D. E., & Wijffels, R. H. (2012) · Journal of Applied Phycology · doi:10.1007/s10811-012-9954-6 · Cited by 47
Substrate specificity of the violaxanthin de-epoxidase of the primitive green alga Mantoniella squamata (Prasinophyceae)
Goss, R. (2003) · Planta · doi:10.1007/s00425-003-1044-1 · Cited by 46
Contrasting NPQ dynamics and xanthophyll cycling in a motile and a non‐motile intertidal benthic diatom
Blommaert, L., Huysman, M. J. J., Vyverman, W., Lavaud, J., & Sabbe, K. (2017) · Limnology and Oceanography · doi:10.1002/lno.10511 · Cited by 45
The xanthophyll cycle in diatom Phaeodactylum tricornutum in response to light stress
Kuczyńska, P., Jemioła‐Rzemińska, M., Nowicka, B., Jakubowska, A., Strzałka, W., Burda, K., & Strzałka, K. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.04.043 · Cited by 44
Functional heterogeneity of the fucoxanthins and fucoxanthin-chlorophyll proteins in diatom cells revealed by their electrochromic response and fluorescence and linear dichroism spectra
Szabó, M., Premvardhan, L. L., Bernard, L., Goss, R., Wilhelm, C., & Garab, G. (2010) · Chemical Physics · doi:10.1016/j.chemphys.2010.03.001 · Cited by 41
Carotenoid Profile of Edible Japanese Seaweeds: An Improved HPLC Method for Separation of Major Carotenoids
Terasaki, M., Narayan, B., Kamogawa, H., Nomura, M., Stephen, N. M., Kawagoe, C., Hosokawa, M., & Miyashita, K. (2012) · Journal of Aquatic Food Product Technology · doi:10.1080/10498850.2011.610025 · Cited by 40
A model of photosynthesis and photo‐protection based on reaction center damage and repair
Ross, O. N., Moore, C. M., Suggett, D., MacIntyre, H. L., & Geider, R. J. (2008) · Limnology and Oceanography · doi:10.4319/lo.2008.53.5.1835 · Cited by 37
THE IMPACT OF NONPHOTOCHEMICAL QUENCHING OF FLUORESCENCE ON THE PHOTON BALANCE IN DIATOMS UNDER DYNAMIC LIGHT CONDITIONS1
Su, W., Jakob, T., & Wilhelm, C. (2012) · Journal of Phycology · doi:10.1111/j.1529-8817.2012.01128.x · Cited by 35
Utilizing the Effective Xanthophyll Cycle for Blooming of Ochromonas smithii and O. itoi (Chrysophyceae) on the Snow Surface
Tanabe, Y., Shitara, T., Kashino, Y., Hara, Y., & Kudoh, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0014690 · Cited by 31
The response of carotenoids and chlorophylls during virus infection of Emiliania huxleyi (Prymnesiophyceae)
Llewellyn, C. A., Evans, C., Airs, R. L., Cook, I., Bale, N. J., & Wilson, W. H. (2007) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2006.12.013 · Cited by 33
PHOTOPROTECTION OF SEA‐ICE MICROALGAL COMMUNITIES FROM THE EAST ANTARCTIC PACK ICE1
Petrou, K., Hill, R., Doblin, M. A., McMinn, A., Johnson, R. W., Wright, S. W., & Ralph, P. J. (2011) · Journal of Phycology · doi:10.1111/j.1529-8817.2010.00944.x · Cited by 30
Carotenoid metabolism in phytoplankton
Lohr, M. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511732263.006 · Cited by 31
Responses ofEmiliania huxleyi(Prymnesiophyceae) to step changes in photon flux density
Harris, G. N., Scanlan, D. J., & Geider, R. J. (2009) · European Journal of Phycology · doi:10.1080/09670260802233460 · Cited by 30
High light stress and the one-helix LHC-like proteins of the cryptophyte Guillardia theta
Funk, C., Alami, M., Tibiletti, T., & Green, B. R. (2011) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2011.03.011 · Cited by 30
Diadinoxanthin de‐epoxidation as important factor in the short‐term stabilization of diatom photosynthetic membranes exposed to different temperatures
Bojko, M., Olchawa‐Pajor, M., Goss, R., Schaller, S., Strzałka, K., & Latowski, D. (2018) · Plant Cell & Environment · doi:10.1111/pce.13469 · Cited by 27
A rapid aureochrome opto-switch enables diatom acclimation to dynamic light
Zhang, H., Xiong, X., Guo, K., Zheng, M., Cao, T., Yang, Y., Song, J., Cen, J., Zhang, J., Jiang, Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49991-7 · Cited by 29
PHOTOPHYSIOLOGICAL PROPERTIES OF THE MARINE PICOEUKARYOTE PICOCHLORUM RCC 237 (TREBOUXIOPHYCEAE, CHLOROPHYTA)1
Dimier, C., Corato, F., Giovanni, S., & Brunet, C. (2007) · Journal of Phycology · doi:10.1111/j.1529-8817.2007.00327.x · Cited by 27
Multi-Omics Analyses Provide Insight into the Biosynthesis Pathways of Fucoxanthin in Isochrysis Galbana
Chen, D., Yuan, X. T., Zheng, X., Fang, J., Lin, G., Li, R., Chen, J., He, W., Huang, Z. J., Fan, W., et al. (2022) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2022.05.010 · Cited by 27
Efficient Heterologous Transformation of Chlamydomonas reinhardtii npq2 Mutant with the Zeaxanthin Epoxidase Gene Isolated and Characterized from Chlorella zofingiensis
Couso, I., Cordero, B. F., Vargas, M. A., & Rodrı́guez, H. (2012) · Marine Drugs · doi:10.3390/md10091955 · Cited by 25
The photobiology of Heterosigma akashiwo. Photoacclimation, diurnal periodicity, and its ability to rapidly exploit exposure to high light
Hennige, S., Coyne, K. J., MacIntyre, H. L., Liefer, J. D., & Warner, M. E. (2013) · Journal of Phycology · doi:10.1111/jpy.12043 · Cited by 24
Influence of pH, Mg2+, and lipid composition on the aggregation state of the diatom FCP in comparison to the LHCII of vascular plants
Schaller, S., Richter, K., Wilhelm, C., & Goss, R. (2013) · Photosynthesis Research · doi:10.1007/s11120-013-9951-x · Cited by 23
Photoacclimation to abrupt changes in light intensity by Phaeodactylum tricornutum and Emiliania huxleyi: the role of calcification
Ramos, J. B. E., Schulz, K. G., Febiri, S., & Riebesell, U. (2012) · Marine Ecology Progress Series · doi:10.3354/meps09606 · Cited by 23
Growth and photophysiological responses of two picoplanktonicMinutocellusspecies, strains RCC967 and RCC703 (Bacillariophyceae)
Giovagnetti, V., Cataldo, M. L., Conversano, F., & Brunet, C. (2012) · European Journal of Phycology · doi:10.1080/09670262.2012.733030 · Cited by 20
Both major xanthophyll cycles present in nature promote nonphotochemical quenching in a model diatom
Giossi, C. E., Wünsch, M. A., Dautermann, O., Schober, A. F., Buck, J. M., Kroth, P. G., Lohr, M., & Bernard, L. (2025) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiaf371 · Cited by 19
High fucoxanthin wakame (Undaria pinnatifida) prevents tumor microenvironment formation in an AOM/DSS mouse carcinogenic model
Terasaki, M., Kuramitsu, Y., Kojoma, M., Kim, S.-Y., Tanaka, T., Maeda, H., Miyashita, K., Kawagoe, C., Kohno, S., & Mutoh, M. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.103709 · Cited by 18
Optimising conditions for growth and xanthophyll production in continuous culture of Tisochrysis lutea using photobioreactor arrays and central composite design experiments
Beuzenberg, V., Goodwin, E., Puddick, J., Romanazzi, D., Adams, S. L., & Packer, M. A. (2016) · New Zealand Journal of Botany · doi:10.1080/0028825x.2016.1238398 · Cited by 16
Algal Carotenoids
Jain, A., & Vavilala, S. L. (2020) · Wiley eBooks · doi:10.1002/9781119143802.ch2 · Cited by 16
On the ecology of cold-water phytoplankton in the Baltic Sea
Spilling, K. (2007) · Työväentutkimus Vuosikirja · Cited by 16
Diurnal changes of photoadaptive pigments in microphytobenthos
Jordan, L., McMinn, A., & THOMPSON, P. A. (2009) · Journal of the Marine Biological Association of the United Kingdom · doi:10.1017/s0025315409990816 · Cited by 15
EFFECTS OF TWO MOTILITY INHIBITORS ON THE PHOTOSYNTHETIC ACTIVITY OF THE DIATOMSCYLINDROTHECA CLOSTERIUMANDPLEUROSIGMA ANGULATUM
Cartaxana, P., Brotas, V., & Serôdio, J. (2008) · Diatom Research · doi:10.1080/0269249x.2008.9705737 · Cited by 15
Carotenoid Biosynthesis in Dunaliella (Chlorophyta)
Jin, E., & Polle, J. W. (2009) · Science Publishers eBooks · doi:10.1201/b10300-7 · Cited by 16
Chlorophylls c—Occurrence, synthesis, properties, photosynthetic and evolutionary significance
Myśliwa-Kurdziel, B., Latowski, D., & Strzałka, K. (2019) · Advances in Botanical Research · doi:10.1016/bs.abr.2019.04.002 · Cited by 9
Community Vertical Composition of the Laguna Negra Hypersaline Microbial Mat, Puna Region (Argentinean Andes)
Boidi, F. J., Mlewski, E. C., Fernández, G., Flores, M. R., Gérard, E., Farı́as, M. E., & Gómez, F. J. (2022) · Biology · doi:10.3390/biology11060831 · Cited by 13
Ocean acidification affects pigment concentration and photoprotection of marine phytoplankton
Alcaraz‐Rocha, P., Puig‐Fàbregas, J., Garrido, J. L., & Sobrino, C. (2023) · Limnology and Oceanography · doi:10.1002/lno.12313 · Cited by 13
Photoacclimation impacts the molecular features of photosystem supercomplexes in the centric diatom Thalassiosira pseudonana
Calvaruso, C., Stefanidis, K., & Büchel, C. (2022) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2022.148589 · Cited by 13
On the Relationship between a Novel Prorocentrum sp. and Colonial Phaeocystis antarctica under Iron and Vitamin B12 Limitation: Ecological Implications for Antarctic Waters
Bolinesi, F., Saggiomo, M., Aceto, S., Cordone, A., Serino, E., Valoroso, M. C., & Mangoni, O. (2020) · Applied Sciences · doi:10.3390/app10196965 · Cited by 13
Xanthophyll cycling and fucoxanthin biosynthesis in the model diatom Phaeodactylum tricornutum: recent advances and new gene functions
Giossi, C. E., Kroth, P. G., & Bernard, L. (2025) · Frontiers in Photobiology · doi:10.3389/fphbi.2025.1680034 · Cited by 12

Authors: Lohr, M., & Wilhelm, C.
Affiliations: Leipzig University (DE)
ORCID: Lohr, Martin
Wilhelm, Christian
Venue: Planta
Publisher: Springer Science and Business Media LLC
Published: 2001-02-19
Volume: 212
Issue: 3
Pages: 382-391
ISSN: 0032-0935 (ISSN-L)
1432-2048
DOI: 10.1007/s004250000403
OpenAlex: W2016123825
Cited by: 152
References: 42
Citations by year: 2026: 3 · 2025: 4 · 2024: 9 · 2023: 10 · 2022: 10 · 2021: 5 · 2020: 12 · 2019: 7 · 2018: 2 · 2017: 6 · 2016: 3 · 2015: 3 · 2014: 3 · 2013: 6 · 2012: 13
FWCI: 0.58
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Planta (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Algal biology and biofuel production
Keywords: xanthophyll biosynthesis, diatoms, Phaeodactylum tricornutum, Cyclotella meneghiniana, violaxanthin, beta-cryptoxanthin, zeaxanthin, diadinoxanthin, fucoxanthin, xanthophyll cycle, mathematical model, light acclimation, beta-carotene
MeSH terms: Antioxidants, Carotenoids, Chromatography, High Pressure Liquid, Dithioerythritol, Epoxy Compounds, Herbicides, Light, Models, Biological, Pigments, Biological, Pyridazines, Sulfhydryl Reagents, Lutein, Diatoms, beta Carotene, Xanthophylls, Zeaxanthins, Cryptoxanthins

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Xanthophyll synthesis in diatoms: quantification of putative intermediates and comparison of pigment conversion kinetics with rate constants derived from a model

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks