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Phyllobilins

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Phyllobilins (PBs) are linear tetrapyrroles generated by the metabolic breakdown of chlorophyll in plants.[1] They are products of the pheophorbide a oxygenase/phyllobilin (PAO/PB) pathway of natural chlorophyll breakdown,[2] and are distantly related to the bilins resulting from heme breakdown, such as bilirubin. Chlorophyll breakdown is a massive phenomenon, most visual when the fall colors arise, producing each year about 109 tons of PBs worldwide.[3] Strikingly, despite its obvious importance, chlorophyll breakdown has long remained enigmatic, as the search for its expected tetrapyrrolic products has been futile.[4] By 1991, organic chemist Bernhard Kräutler, botanist Philippe Matile, and their teams succeeded in unambiguously identifying a first chlorophyll catabolite from plants (then called RP-14) and elucidating its striking structure.[5] This first, colorless PB from de-greened cotyledons of barley (Hordeum vulgare) was classified as a non-fluorescent chlorophyll catabolite (NCC) and given the provisional name Hv-NCC-1 (fig. 1).[6] A colorless, but fluorescent PB found in oil seed rape, subsequently characterized and named "primary" FCC (pFCC),[7] is a formal precursor of Hv-NCC-1, and has a structure more similar to pheophorbide a (Pheo a). The pFCC-structure highlights the critical cleavage of the porphyrinoid macrocycle of chlorophyll (fig. 1) in the course of chlorophyll breakdown in plants.[2]

Figure 1. Chlorophylls a and b; pheophorbide a (Pheo a) and two colorless phyllobilins (PBs) (chromophores marked in bold) identified as natural chlorphyll (Chl) degradation products. PBs are depicted in a pseudo-cyclic presentation, with bilin-type atom numbering and ring labelling, different from that in chlorophylls

Nomenclature

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Figure 2. Name-giving phyllobilane core element, displayed in stretched (left) and in pseudo-cyclic presentation (right)[1]

Original names of the PBs have been phenomenological, short acronyms, specifying their plant source and structure-type, such as Hv-NCC-1.[2] A structure-based nomenclature named the tetrapyrrolic chlorophyll catabolites as 4,5-dioxo-4,5-seco-phytoporphyrinates, i.e., as between C4 and C5 ring-opened derivatives of Pheo a.[5] Accordingly, pFCC is a 31,32-didehydro-1,4,5,10,17,18,20-(22H)-octahydro-132-methoxycarbonyl-4,5-dioxo-4,5-seco-phytoporphyrinate.[7] Since 2014, when linear tetrapyrroles from Chl-breakdown were classified as "phyllobilins" (PBs) by Kräutler, previous names were replaced by a phyllobilane-based semi-systematic nomenclature (fig. 2),[note 1] as recommended for linear tetrapyrroles by the International Union of Pure and Applied Chemistry[8] (e.g., for the heme-derived bilins[9]). In consequence, pFCC is a (10Z)-1-formyl-19-oxo-12,13,16,19-tetrahydro-phyllobilene-b.

With the discovery of two 1,19-dioxo-phyllobilins that were structurally related to Hv-NCC-1, a puzzling altered type of phyllobilins became known (2001,[10] 2011[11]), to be established (only in 2013) as first representatives of an important second branch of chlorophyll breakdown in some plants.[12] Since then, PBs are classified either as type-I PBs (1-formyl-19-oxo-phyllobilins), or as type-II PBs (1,19-dioxo-phyllobilins). Nowadays, over 80 different natural PBs (including their synthetic metal complexes) are known.[6][13]

Colorless phyllolumibilins and phylloleucobilins

[edit]

The two basic types of the important colorless phyllobilins in plants are the (nonfluorescent) phylloleucobilins and (fluorescent) phyllolumibilins. They carry a remarkable variety of functional groups at the periphery of their tetrapyrrole cores, typically increasing their polarity (fig. 3 and table). The colorless PBs represent the major group of the known natural PBs.[6][13] A hydroxyl group attached at C32 is the first one of the substituents introduced at the stage of the primary FCCs (pFCCs), giving the corresponding secondary FCCs (sFCCs). Further modifications are deduced to furnish a variety of modified FCCs (mFCCs, fig. 3). In fact, typical FCCs are only fleetingly existent catabolites and isomerize non-enzymatically in aqueous environment to the corresponding NCCs, 82S,10R-isomers, as, e.g., Hv-NCC-1.[14] Hence, with few exceptions, the peripheral modifications were only detected in NCCs (figs. 1, 3).[6]

Figure 3. Chemical formulas of colorless type-I PBs and type-II PBs in pseudo-cyclic presentation. Fluorescent phyllolumibilins (top): secondary FCC (sFCC), hypothetical modified FCCs (mFCCs) and DFCCs (e.g., At-DFCC-33); bottom: corresponding non-fluorescent phylloleucobilins: NCCs (see table for R1–R3) and DNCCs (R1 = H, OH; R2 = H, CH3; R3 = vinyl, CH(OH)-CH2(OH))
 Major substitution patterns of NCCs (see general formula in fig. 3)[6]
R1 R2 R3 Original name
H  H  CH=CH2 Bo-NCC-2[15]
H H  CH=CH2 At-NCC-3[a][16]
H CH3 CH=CH2 Cj-NCC-2[14]
OH H CH=CH2 Bn-NCC-3[17]
OH H CH(OH)-CH2OH So-NCC-1[18]
OH CH3 CH=CH2 Cj-NCC-1[19][14]
OH CH3 CH(OH)-CH2OH Hv-NCC-1[5]
O-Glc[b] H CH=CH2 Bn-NCC-2[17]
O-Glc CH3 CH=CH2 Nr-NCC-2[20]
O-Glc CH3 CH(OH)-CH2OH Zm-NCC-1[21]
O-Glc CH3 CH(OH)-CH2O-Glc Pd-NCC-32[22]
O-Mal[c] H  CH=CH2 Bn-NCC-1[17]
O-MalGlc CH3 CH=CH2 Nr-NCC-1[20]
[a] Exceptionally, At-NCC-3 carries a CH2-OH group at C2 (instead of methyl); [b] Glc = β-D-glucopyranosyl; [c] Mal = malonyl
Source species: At = Arabidopsis thaliana, Bn = Brassica napus, Bo = Brassica oleracea var. Italica, Cj = Cercidiphyllum japonicum, Hv = Hordeum vulgare, Nr = Nicotiana rustica, Pd = Prunus domestica ssp. domestica, So = Spinacia oleracea, Zm = Zea mays

When pFCC was identified, its configuration at C16 could not be characterized,[7] and was later classified provisionally as n.[6] In fact, the "primary" FCCs are generated plant-specifically, either as pFCC, C16n (fig. 1), or as epi-pFCC, with epi-configuration at C16, and both C16-epimeric FCCs exist naturally. Hydroxylation at C32 of the respective primary FCC occurs irrespective of its C16 configuration: sFCC is derived from pFCC, epi-sFCC from epi-pFCC. NCCs inherit their configuration at C16 from their precursor FCCs; hence, Hv-NCC-1 is C16n, as it is derived from pFCC via sFCC.[6]

Oxidative removal of the 1-formyl function of the sFCC was deduced to generate the sDFCC, the cryptic natural methyl ester that is rapidly demethylated enzymatically (in Arabidopsis thaliana) to At-DFCC-33, a first DFCC, actually isolated from a leaf (fig. 3).[12] At-DFCC-33 isomerizes rapidly to the corresponding DNCC,[23] opening up access to further downstream 1,19-dioxo-phyllobilins in A. thaliana. In view of the existence of two important breakdown paths, the PBs are now classified either as type-I PBs (1-formyl-19-oxo-phyllobilins) or as type-II PBs (1,19-dioxo-phyllobilins).[6]

Figure 4. Chemical formulas of representative hmFCCs from bananas: Mc-FCC-56 (from fruit) and Ma-FCC-114 (from leaf) of Musa acuminata, in pseudo-cyclic presentation (left), and of the fluorescent bicyclo-phyllobilin (Vv-FCC-55) from grapevine leaves (Vitis vinifera) having a bicyclo-glycoside appendage (right)

In contrast to typical FCCs (fig. 3), so called hypermodified fluorescent FCCs (hmFCCs), first discovered in ripening bananas as, e.g., Mc-FCC-56, (fig. 4) are uniquely persistent.[24] They accumulate as blue fluorescent natural "optical brighteners" in some ripening fruit, a particularly intriguing feature of de-greened banana fruits, and in senescent banana leaves.[6] Among the hmFCCs, lipophilic derivatives have been found,[25] such as Ma-FCC-114[26] that contains parts of a main chloroplast membrane constituent.[27]

An exceptional hmFCC variant is represented by phyllolumibilins with a bicyclo-glycoside appendage, such as Vv-FCC-55, isolated from grapevine leaves. In this phyllolumibilin, a 1',6'-glucose link is "bridging" between its carboxyl-O124 and hydroxyl-O33 in a remarkable macrocycle (fig. 4 right).[28]

Colored phyllobilins: phyllochromobilins

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The first natural phyllochromobilins detected in senescent leaves are yellow chlorophyll catabolites (YCCs, fig. 5), observed in extracts of degreened leaves of the deciduous tree Cercidiphyllum japonicum.[29] One of these YCCs, named Cj-YCC-2, has also become accessible effectively by partial chemical oxidation[29] of its natural precursor, Cj-NCC-1.[19] In a similar way, DYCCs have been prepared from DNCCs, using chemical or endogenous, natural synthesis with homogenates of senescent leaves.[30] YCCs and DYCCs represent the class of phylloxanthobilins. Their more stable Z-isomers exhibit very similar blue light absorption with a maximum near 430 nm.[31] Phylloxanthobilins (Z/E) photo-isomerize readily at their C15-C16 double bond,[32] similar to their analog bilirubin.[33]

Figure 5. Representative phyllochromobilins, type-I PBs (left) and type-II PBs (right), shown with chromophores marked in bold. Top: 15Z-isomers of yellow chlorophyll catabolites (YCCs and DYCCs) depicted in pseudo-cyclic display; bottom: pink PiCCs and DPiCCs presented in their main 10E,15Z- conformation

Phylloxanthobilins[note 1] (YCCs and DYCCs) are excellent antioxidants,[34] and their air oxidation generates pink phylloroseobilins (type-I PiCCs and type-II DPiCCs) (fig. 5) absorbing light near 520 nm.[6] The oxidation of the Zn-complex of Cj-YCC-2 leads to the corresponding Zn-PiCC, which loses its Zn-ion upon treatment with phosphate, providing an efficient path to pure Cj-PiCC.[35] The type-II phylloroseobilin DPiCC was synthesized[36] analogously from the corresponding DYCC.[31]

When isolated pure, several phyllochromobilins could be crystallized. This allowed for the first x-ray crystal structure analysis of a chlorophyll-derived PB from a higher plant, carried out with Cj-PiCC. It confirmed its spectroscopically derived structure, giving detailed insights into the actual molecular geometry of the PiCC as 10E,15Z-isomer.[35][37][38] Another crystal structure determination dealt with the methyl ester of Cj-YCC-2,[32][39] confirming the stereochemical assignment of this YCC as a 10Z-isomer, and establishing its (R)-configuration at C10. Simultaneously, this analysis provided convincing evidence for the 82(S)[40] and the earlier proposed 10(R) stereochemistry[14] in the prevailing epimers of natural NCCs (see fig. 5).[41] Likewise, a first crystal structure of a pyro-YCC, lacking the chlorophyll-typical methyl ester group at C82 (see fig. 5), was determined.[42][43] The two YCC crystal structures showed dimers with "double-decker arrangements" due to π-stacking of the conjugated system spanning rings C and D (fig. 5), assisted by hydrogen bonding. Depending on the polarity of the solvent, this stacking in dimers was also observed in solution by 1H NMR.[32][42]

Phyllobilin metal complexes

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While complexation of NCCs and DNCCs has not been observed (nor expected), phyllochromobilins are excellent ligands for transition-metal ions.[38] Phylloroseobilins bind the metal ions Zn2+ and Cd2+ particularly well in monomeric blue complexes that exhibit a strong red fluorescence:[6][32][44] M(II)-PiCCs (M=Zn, Cd, Ni, Cu),[35] and Zn(II)-DpiCCs.[44] Zn(II) ions coordinate the methyl ester of Cj-YCC-2, a bidentate ligand, in a 2:1 assembly.[45]

Iso-phyllobilanones (iPBs): PBs with a rearranged backbone

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Figure 6. iso-Phyllobilanones (iPBs; R = H, OH) with re-arranged ring B (left), and a 12,13-dioxo-12,13-seco-iPB from further oxidative opening of ring C (right)

Instead of the common PBs found in angiosperms, in the cryptogam eagle fern, first representative iso-phyllobilanones (iPBs) have been found, featuring a second basic carbon backbone in chlorophyll catabolites.[46] It displays a rearranged tetrapyrrole skeleton, with ring B linked to ring A at the β-carbon and transformed into a five-membered-ring lactam. It also lacks the carboxylate functions at ring E of the known natural PBs from higher plants (fig. 6).[46] Other iPBs from the fern are strikingly reactive 12,13-dioxo-12,13-seco-iPBs (siPBs), in which the (former) ring C is also cleaved (fig. 6 ).[47]

iPB structures show the exact cleavage pattern of the chlorophyll macrocycle characteristic for PBs from angiosperms and are further restructured by the C6-C7 oxidative rearrangement. However, they lack most of the typical further modifications of the PBs from angiosperms. iPBs are considered to reflect evolutionary developments of chlorophyll breakdown in green plants in the Paleozoic era.[47][48]

Biological activities of phyllobilins

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Originally, chlorophyll breakdown was rationalized in simple terms as a detoxification process.[3][49] However, ripening of most fruits that we eat is accompanied by degreening, i.e., breakdown of chlorophyll, and the appearance of appealing colors. In consequence, attention was given to the chlorophyll catabolites in ripening apples and pears.[50] They were found to be NCCs identical to those from senescent leaves. When tested in a standard autoxidation experiment of a type used for the analysis of bilirubin,[33] a known antioxidant, NCCs were found to be only slightly inferior to the latter and their consumption was proposed to be potentially beneficial for human health.[50][51]

The massive amounts of diverse PBs generated by chlorophyll breakdown are nowadays understood differently, considering the intriguing bioactivities that PBs may have:[52] they are investigated as a natural product class with biologically, chemically and pharmacologically interesting properties.[13][53] In pioneering work by Simone Moser[54] and her group, biologically active[55][56][57] and pharmacologically interesting linear tetrapyrroles[58][13] have been investigated with respect to their antioxidative,[34][59] immunomodulatory,[34] anti-inflammatory,[59] and anti-cancer activities,[60] in particular.

Notes

[edit]
  1. 1 2 Phyllobilin (PB)[61][1] is used as a generic name for the entire class of tetrapyrrolic chlorophyll catabolites from plants in analogy to bilin: colorless, non-fluorescing phyllobilanes (NCCs, DNCCs), featuring completely deconjugated pyrrole rings, were also classified as phylloleucobilins;[6] the partially deconjugated phyllobilenes-b (fluorescing FCCs, hmFCCs, DFCCs) as phyllolumibilins; partially deconjugated phyllobilenes-c (YCCs, DYCCs) as phylloxanthobilins; phyllobiladienes-b,c (PiCCs, DPiCCs) as phylloroseobilins.[6] – Phyllobilins are not to be mixed up with phycobilins[62] and phytobilins, which are heme-degradation products originating biosynthetically from biliverdin, and are unsaturated, conjugated linear tetrapyrroles used as chromophores to capture light in photosynthetic and (as phytochromes) in photoregulatory processes.

References

[edit]
  1. 1 2 Kräutler, Bernhard (2014). "Phyllobilins – the Abundant Tetrapyrrolic Catabolites of the Green Plant Pigment Chlorophyll". Chemical Society Reviews. 43 (17): 6227–6238. doi:10.1039/C4CS00079J. ISSN 1460-4744.
  2. 1 2 3 Hörtensteiner, Stefan; Hauenstein, Mareike; Kräutler, Bernhard (2019). "Chapter seven - Chlorophyll Breakdown – Regulation, Biochemistry and Phyllobilins as its Products Metabolism, Structure and Function of Plant Tetrapyrroles". In Grimm, Bernhard (ed.). Metabolism, Structure and Function of Plant Tetrapyrroles: Introduction, Microbial and Eukaryotic Chlorophyll Synthesis and Catabolism. Advances in Botanical Research. Vol. 90. Elsevier. pp. 213–271. doi:10.1016/bs.abr.2019.03.004. ISBN 978-0-08-102752-3. ISSN 0065-2296.
  3. 1 2 Kräutler, Bernhard; Matile, Philippe (1999). "Solving the Riddle of Chlorophyll Breakdown". Accounts of Chemical Research. 32 (1): 35–43. doi:10.1021/ar970225n. ISSN 0001-4842.
  4. ↑ Hendry, George A. F.; Houghton, Jennifer D.; Brown, Stanley B. (1987). "Tansley Review No. 11. The Degradation of Chlorophyll-A Biological Enigma". The New Phytologist. 107 (2): 255–302. ISSN 0028-646X.
  5. 1 2 3 Kräutler, Bernhard; Jaun, Bernhard; Bortlik, Karlheinz; Schellenberg, Maja; Matile, Philippe (1991). "On the Enigma of Chlorophyll Catabolism – The Constitution of a Secoporphinoid Catabolite". Angewandte Chemie, International Edition in English. 30 (10): 1315–1318. doi:10.1002/anie.199113151. ISSN 0570-0833.
  6. 1 2 3 4 5 6 7 8 9 10 11 Kräutler, Bernhard (2016). "Breakdown of Chlorophyll in Higher Plants—Phyllobilins as Abundant, Yet Hardly Visible Signs of Ripening, Senescence, and Cell Death". Angewandte Chemie, International Edition. 55 (16): 4882–4907. doi:10.1002/anie.201508928. ISSN 1433-7851. PMC 4950323. PMID 26919572.
  7. 1 2 3 Mühlecker, Walter; Ongania, Karl-Hans; Kräutler, Bernhard; Matile, Philippe; Hörtensteiner, Stefan (1997). "Tracking Down Chlorophyll Breakdown in Plants: Elucidation of the Constitution of a "Fluorescent" Chlorophyll Catabolite". Angewandte Chemie, International Edition in English. 36 (4): 401–404. doi:10.1002/anie.199704011. ISSN 0570-0833.
  8. ↑ "TP-6 and TP-7 Linear Tetrapyrroles". Nomenclature of Tetrapyrroles. Retrieved 31 January 2026.
  9. ↑ Falk, Heinz (1989). Chemistry of Linear Oligopyrroles and Bile Pigments (in German). Wien: Springer. ISBN 3211821120.
  10. ↑ Losey, Fosca Gattoni; Engel, Norbert (2001). "Isolation and Characterization of a Urobilinogenoidic Chlorophyll Catabolite from Hordeum vulgare L." Journal of Biological Chemistry. 276 (12): 8643–8647. doi:10.1074/jbc.M009288200.
  11. ↑ Müller, Thomas; Rafelsberger, Martina; Vergeiner, Clemens; Kräutler, Bernhard (2011). "A Dioxobilane as Product of a Divergent Path of Chlorophyll Breakdown in Norway Maple". Angewandte Chemie, International Edition. 50 (45): 10724–10727. doi:10.1002/anie.201103934. ISSN 1433-7851. PMC 3262146. PMID 21928453.
  12. 1 2 Christ, Bastien; Süssenbacher, Iris; Moser, Simone; Bichsel, Nicole; Egert, Aurelie; Müller, Thomas; Kräutler, Bernhard; Hörtensteiner, Stefan (2013). "Cytochrome P450 CYP89A9 Is Involved in the Formation of Major Chlorophyll Catabolites during Leaf Senescence in Arabidopsis". The Plant Cell. 25 (5): 1868–1880. doi:10.1105/tpc.113.112151. ISSN 1532-298X. PMC 3694711. PMID 23723324.
  13. 1 2 3 4 Karg, Cornelia A.; Taniguchi, Masahiko; Lindsey, Jonathan S.; Moser, Simone (2023). "Phyllobilins – Bioactive Natural Products Derived from Chlorophyll – Plant Origins, Structures, Absorption Spectra, and Biomedical Properties". Planta Medica. 89 (06): 637–662. doi:10.1055/a-1955-4624. ISSN 0032-0943.
  14. 1 2 3 4 Oberhuber, Michael; Berghold, Joachim; Breuker, Kathrin; Hörtensteiner, Stefan; Kräutler, Bernhard (2003). "Breakdown of chlorophyll: A nonenzymatic reaction accounts for the formation of the colorless "nonfluorescent" chlorophyll catabolites". Proceedings of the National Academy of Sciences. 100 (12): 6910–6915. doi:10.1073/pnas.1232207100. ISSN 0027-8424. PMC 165803. PMID 12777622.
  15. ↑ Roiser, Matthias H.; Müller, Thomas; Kräutler, Bernhard (2015). "Colorless Chlorophyll Catabolites in Senescent Florets of Broccoli (Brassica oleracea var. italica)". Journal of Agricultural and Food Chemistry. 63 (5): 1385–1392. doi:10.1021/jf5055326. ISSN 0021-8561. PMC 4329831. PMID 25620234.
  16. ↑ Müller, Thomas; Moser, Simone; Ongania, Karl‐Hans; Pružinská, Adriana; Hörtensteiner, Stefan; Kräutler, Bernhard (2006). "A Divergent Path of Chlorophyll Breakdown in the Model Plant Arabidopsis thaliana". ChemBioChem. 7 (1): 40–42. doi:10.1002/cbic.200500268. ISSN 1439-4227.
  17. 1 2 3 Mühlecker, Walter; Kräutler, Bernhard (1996). "Breakdown of Chlorophyll: Constitution of nonfluorescing chlorophyll-catabolites from senescent cotyledons of the dicot rape". Plant Physiology and Biochemistry (Issy-les-Moulineaux, France). 34 (1): 61–75. ISSN 0981-9428.
  18. ↑ Berghold, Joachim; Breuker, Kathrin; Oberhuber, Michael; Hörtensteiner, Stefan; Kräutler, Bernhard (2002). "Chlorophyll breakdown in spinach: on the structure of five nonfluorescent chlorophyll catabolites". Photosynthesis Research. 74 (2): 109–119. doi:10.1023/A:1020991023248. ISSN 0166-8595.
  19. 1 2 Curty, Christophe; Engel, Norbert (1996). "Detection, isolation and structure elucidation of a chlorophyll a catabolite from autumnal senescent leaves of Cercidiphyllum japonicum". Phytochemistry. 42 (6): 1531–1536. doi:10.1016/0031-9422(96)00155-0.
  20. 1 2 Berghold, Joachim; Eichmüller, Christian; Hörtensteiner, Stefan; Kräutler, Bernhard (2004). "Chlorophyll Breakdown in Tobacco: On the Structure of Two Nonfluorescent Chlorophyll Catabolites". Chemistry & Biodiversity. 1 (4): 657–668. doi:10.1002/cbdv.200490057. ISSN 1612-1872.
  21. ↑ Berghold, Joachim; Müller, Thomas; Ulrich, Markus; Hörtensteiner, Stefan; Kräutler, Bernhard (2006). "Chlorophyll Breakdown in Maize: On the Structure of Two Nonfluorescent Chlorophyll Catabolites". Monatshefte für Chemie - Chemical Monthly. 137 (6): 751–763. doi:10.1007/s00706-006-0473-5. ISSN 0026-9247.
  22. ↑ Erhart, Theresia; Mittelberger, Cecilia; Vergeiner, Clemens; Scherzer, Gerhard; Holzner, Barbara; Robatscher, Peter; Oberhuber, Michael; Kräutler, Bernhard (2016). "Chlorophyll Catabolites in Senescent Leaves of the Plum Tree (Prunus domestica)". Chemistry & Biodiversity. 13 (11): 1441–1453. doi:10.1002/cbdv.201600181. ISSN 1612-1872. PMC 5123584. PMID 27533340.
  23. ↑ Süssenbacher, Iris; Hörtensteiner, Stefan; Kräutler, Bernhard (2015). "A Dioxobilin-Type Fluorescent Chlorophyll Catabolite as a Transient Early Intermediate of the Dioxobilin-Branch of Chlorophyll Breakdown in Arabidopsis thaliana". Angewandte Chemie, International Edition. 54 (46): 13777–13781. doi:10.1002/anie.201506299. ISSN 1433-7851. PMC 4678512. PMID 26426977.
  24. ↑ Moser, Simone; Müller, Thomas; Ebert, Marc‐Olivier; Jockusch, Steffen; Turro, Nicholas J.; Kräutler, Bernhard (2008). "Blue Luminescence of Ripening Bananas". Angewandte Chemie, International Edition. 47 (46): 8954–8957. doi:10.1002/anie.200803189. ISSN 1433-7851. PMC 2912500. PMID 18850621.
  25. ↑ Banala, Srinivas; Moser, Simone; Müller, Thomas; Kreutz, Christoph; Holzinger, Andreas; Lütz, Cornelius; Kräutler, Bernhard (2010). "Hypermodified Fluorescent Chlorophyll Catabolites: Source of Blue Luminescence in Senescent Leaves". Angewandte Chemie, International Edition. 49 (30): 5174–5177. doi:10.1002/anie.201000294. ISSN 1433-7851. PMC 2923073. PMID 20533476.
  26. ↑ Vergeiner, Clemens; Kräutler, Bernhard (2026). "A Novel Type of Fluorescent Chlorophyll Catabolites Hypermodified by Lipophilic Chloroplast Membrane Components". Helvetica Chimica Acta. 109 (5). doi:10.1002/hlca.70071. ISSN 0018-019X.
  27. ↑ Hölzl, Georg; Dörmann, Peter (29 April 2019). "Chloroplast Lipids and Their Biosynthesis". Annual Review of Plant Biology. 70 (1): 51–81. doi:10.1146/annurev-arplant-050718-100202. ISSN 1543-5008.
  28. ↑ Erhart, Theresia; Mittelberger, Cecilia; Liu, Xiujun; Podewitz, Maren; Li, Chengjie; Scherzer, Gerhard; Stoll, Gertrud; Valls, Josep; Robatscher, Peter; Liedl, Klaus R.; Oberhuber, Michael; Kräutler, Bernhard (2018). "Novel Types of Hypermodified Fluorescent Phyllobilins from Breakdown of Chlorophyll in Senescent Leaves of Grapevine (Vitis vinifera)". Chemistry – A European Journal. 24 (65): 17268–17279. doi:10.1002/chem.201803128. ISSN 0947-6539. PMC 6282590. PMID 30079972.
  29. 1 2 Moser, Simone; Ulrich, Markus; Müller, Thomas; Kräutler, Bernhard (2008). "A yellow chlorophyll catabolite is a pigment of the fall colours". Photochemical & Photobiological Sciences. 7 (12): 1577–1581. doi:10.1039/b813558d. ISSN 1474-905X. PMC 2906697. PMID 19037512.
  30. ↑ Vergeiner, Clemens; Ulrich, Markus; Li, Chengjie; Liu, Xiujun; Müller, Thomas; Kräutler, Bernhard (2015). "Stereo- and Regioselective Phyllobilane Oxidation in Leaf Homogenates of the Peace Lily (Spathiphyllum wallisii) : Hypothetical Endogenous Path to Yellow Chlorophyll Catabolites". Chemistry – A European Journal. 21 (1): 13–13. doi:10.1002/chem.201405696. ISSN 0947-6539.
  31. 1 2 Li, Chengjie; Erhart, Theresia; Liu, Xiujun; Kräutler, Bernhard (2019). "Yellow Dioxobilin-Type Tetrapyrroles from Chlorophyll Breakdown in Higher Plants—A New Class of Colored Phyllobilins". Chemistry – A European Journal. 25 (16): 4052–4057. doi:10.1002/chem.201806038. ISSN 0947-6539. PMC 6563717. PMID 30688378.
  32. 1 2 3 4 Li, Chengjie; Wurst, Klaus; Jockusch, Steffen; Gruber, Karl; Podewitz, Maren; Liedl, Klaus R.; Kräutler, Bernhard (2016). "Chlorophyll-Derived Yellow Phyllobilins of Higher Plants as Medium-Responsive Chiral Photoswitches". Angewandte Chemie, International Edition. 55 (51): 15760–15765. doi:10.1002/anie.201609481. ISSN 1433-7851. PMC 5248603. PMID 27891749.
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  34. 1 2 3 Karg, Cornelia A.; Parráková, Lucia; Fuchs, Dietmar; Schennach, Harald; Kräutler, Bernhard; Moser, Simone; Gostner, Johanna M. (2022). "A Chlorophyll-Derived Phylloxanthobilin Is a Potent Antioxidant That Modulates Immunometabolism in Human PBMC". Antioxidants. 11 (10): 2056. doi:10.3390/antiox11102056. ISSN 2076-3921. PMC 9599000. PMID 36290779.
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  36. ↑ Li, Chengjie; Kräutler, Bernhard (2019). "A pink colored dioxobilin-type phyllobilin from breakdown of chlorophyll". Monatshefte für Chemie - Chemical Monthly. 150 (5): 813–820. doi:10.1007/s00706-019-02396-5. ISSN 0026-9247.
  37. ↑ "ZOMKET". Cambridge Structural Database CCDC/Fiz Karlsruhe. doi:10.5517/cc11y4fk. Retrieved 3 March 2026.
  38. 1 2 Li, Chengjie; Kräutler, Bernhard (2015). "Transition metal complexes of phyllobilins – a new realm of bioinorganic chemistry". Dalton Transactions. 44 (22): 10116–10127. doi:10.1039/C5DT00474H. ISSN 1477-9226. PMC 4447063. PMID 25923782.
  39. ↑ "EBEKII". Cambridge Structural Database CCDC/Fiz Karlsruhe. doi:10.5517/ccdc.csd.cc1mcsh8. Retrieved 3 March 2026.
  40. ↑ Moser, Simone; Scherzer, Gerhard; Kräutler, Bernhard (2017). "On the Nature of Isomeric Nonfluorescent Chlorophyll Catabolites in Leaves and Fruit – A Study with a Ubiquitous Phylloleucobilin and its Main Isomerization Product". Chemistry & Biodiversity. 14 (11). doi:10.1002/cbdv.201700368. ISSN 1612-1872.
  41. ↑ Kräutler, Bernhard (2019). "Chlorophyll Breakdown – How Chemistry Has Helped to Decipher a Striking Biological Enigma". Synlett. 30 (03): 263–274. doi:10.1055/s-0037-1611063. ISSN 0936-5214.
  42. 1 2 Li, Chengjie; Wurst, Klaus; Berghold, Joachim; Podewitz, Maren; Liedl, Klaus R.; Kräutler, Bernhard (2018). "Pyro‐Phyllobilins: Elusive Chlorophyll Catabolites Lacking a Critical Carboxylate Function of the Natural Chlorophylls". Chemistry – A European Journal. 24 (12): 2987–2998. doi:10.1002/chem.201705331. ISSN 0947-6539. PMC 5861670. PMID 29244236.
  43. ↑ "XIBSAF". Cambridge Structural Database CCDC/Fiz Karlsruhe. doi:10.5517/ccdc.csd.cc1q27wx. Retrieved 3 March 2026.
  44. 1 2 Li, Chengjie; Podewitz, Maren; Kräutler, Bernhard (2021). "A Blue Zinc Complex of a Dioxobilin-Type Pink Chlorophyll Catabolite Exhibiting Bright Chelation-Enhanced Red Fluorescence". European Journal of Inorganic Chemistry. 2021 (20): 1904–1912. doi:10.1002/ejic.202100206. ISSN 1434-1948.
  45. ↑ Li, Chengjie; Kräutler, Bernhard (2016). "Zn-complex of a natural yellow chlorophyll catabolite". Journal of Porphyrins and Phthalocyanines. 20 (01n04): 388–396. doi:10.1142/S1088424616500176. ISSN 1088-4246.
  46. 1 2 Erhart, Theresia; Vergeiner, Stefan; Kreutz, Christoph; Kräutler, Bernhard; Müller, Thomas (2018). "Chlorophyll Breakdown in a Fern—Discovery of Phyllobilin Isomers with a Rearranged Carbon Skeleton". Angewandte Chemie, International Edition. 57 (45): 14937–14941. doi:10.1002/anie.201807818. ISSN 1433-7851. PMC 6220952. PMID 30144281.
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  48. ↑ Schumacher, Isabel; Menghini, Damian; Ovinnikov, Serguei; Hauenstein, Mareike; Fankhauser, Niklaus; Zipfel, Cyril; Hörtensteiner, Stefan; Aubry, Sylvain (2022). "Evolution of chlorophyll degradation is associated with plant transition to land". The Plant Journal. 109 (6): 1473–1488. doi:10.1111/tpj.15645. ISSN 0960-7412. PMC 9306834. PMID 34931727.
  49. ↑ Pružinská, Adriana; Anders, Iwona; Aubry, Sylvain; Schenk, Nicole; Tapernoux-Lüthi, Esther; Müller, Thomas; Kräutler, Bernhard; Hörtensteiner, Stefan (2007). "In Vivo Participation of Red Chlorophyll Catabolite Reductase in Chlorophyll Breakdown" (PDF). The Plant Cell. 19 (1): 369–387. Bibcode:2007PlanC..19..369P. doi:10.1105/tpc.106.044404. ISSN 1532-298X. PMC 1820978. PMID 17237353.
  50. 1 2 Müller, Thomas; Ulrich, Markus; Ongania, Karl‐Hans; Kräutler, Bernhard (2007). "Colorless Tetrapyrrolic Chlorophyll Catabolites Found in Ripening Fruit Are Effective Antioxidants" (PDF). Angewandte Chemie, International Edition. 46 (45): 8699–8702. doi:10.1002/anie.200703587. ISSN 1433-7851. PMC 2912502. PMID 17943948.
  51. ↑ Moser, Simone; Müller, Thomas; Oberhuber, Michael; Kräutler, Bernhard (2009). "Chlorophyll Catabolites – Chemical and Structural Footprints of a Fascinating Biological Phenomenon". European Journal of Organic Chemistry. 2009 (1): 21–31. doi:10.1002/ejoc.200800804. ISSN 1434-193X. PMC 2965369. PMID 21037946.
  52. ↑ Moser, Simone; Kräutler, Bernhard (2019). "In Search of Bioactivity – Phyllobilins, an Unexplored Class of Abundant Heterocyclic Plant Metabolites from Breakdown of Chlorophyll". Israel Journal of Chemistry. 59 (5): 420–431. doi:10.1002/ijch.201900012. ISSN 0021-2148. PMC 6582504. PMID 31244492.
  53. ↑ Vollmar, Angelika M.; Moser, Simone (2023). "The advent of phyllobilins as bioactive phytochemicals – natural compounds derived from chlorophyll in medicinal plants and food with immunomodulatory activities". Pteridines. 34 (1). doi:10.1515/pteridines-2022-0047. ISSN 2195-4720.
  54. ↑ "Simone Moser. Pharmakognosie". Universität Innsbruck – Department of Pharmacy. Retrieved 15 January 2026. "Simone Moser". Angewandte Chemie, International Edition. 60 (42): 22613–22613. 2021. doi:10.1002/anie.202111178. ISSN 1433-7851. Moser, Simone (2008). The blue luminescence of bananas : novel fluorescent tetrapyrrolic pigments from chlorophyll breakdown (PhD). Universität Innsbruck. Abstract: https://permalink.obvsg.at/AC05039528
  55. ↑ Karg, Cornelia A.; Wang, Shuaijun; Al Danaf, Nader; Pemberton, Ryan P.; Bernard, Denzil; Kretschmer, Maibritt; Schneider, Sabine; Zisis, Themistoklis; Vollmar, Angelika M.; Lamb, Don C.; Zahler, Stefan; Moser, Simone (2021). "Tetrapyrrolic Pigments from Heme‐ and Chlorophyll Breakdown are Actin‐Targeting Compounds". Angewandte Chemie, International Edition. 60 (41): 22578–22584. doi:10.1002/anie.202107813. ISSN 1433-7851. PMC 8519017. PMID 34310831.
  56. ↑ Elvert, Christian A.; Lückenbach, Johanna K. S.; Moser, Simone; Hammerle, Fabian; Karg, Cornelia A. (2025). "Informed Feature-Based Molecular Networking as a Complementary Approach to Identify Bioactive Phyllobilins in Senescent Plant Extracts". ACS Omega. 10 (50): 62312–62321. doi:10.1021/acsomega.5c10395. ISSN 2470-1343. PMC 12750395. PMID 41476507.
  57. ↑ Rütschlin, Sina; Zhang, Lei; Karg, Cornelia A.; Zwerger, Michael; Gostner, Johanna M.; Moser, Simone; Teufel, Robin (2026). "Unexpected Dual Function of Plant YUCCA Enzymes Links Chlorophyll Catabolism to Auxin Homeostasis". Angewandte Chemie, International Edition. 65 (9). doi:10.1002/anie.202525568. ISSN 1433-7851. PMC 12930011. PMID 41560674.
  58. ↑ Wang, Pengyu; Karg, Cornelia A.; Frey, Nadine; Frädrich, Julian; Vollmar, Angelika M.; Moser, Simone (2021). "Phyllobilins as a challenging diverse natural product class: Exploration of pharmacological activities". Archiv der Pharmazie. 354 (10). doi:10.1002/ardp.202100061. ISSN 0365-6233.
  59. 1 2 Frei, Patricia; Nadegger, Christian; Vollmar, Angelika M.; Müller, Thomas; Moser, Simone (2024). "Structural Characterization, and Antioxidative and Anti-inflammatory Activities of Phylloxanthobilins in Tropaeolum majus, a Plant with Relevance in Phytomedicine". Planta Medica. 90 (07/08): 641–650. doi:10.1055/a-2225-8314. ISSN 0032-0943. PMC 11156495. PMID 38843802.
  60. ↑ Karg, Cornelia A.; Wang, Pengyu; Kluibenschedl, Florian; Müller, Thomas; Allmendinger, Lars; Vollmar, Angelika M.; Moser, Simone (2020). "Phylloxanthobilins are Abundant Linear Tetrapyrroles from Chlorophyll Breakdown with Activities Against Cancer Cells". European Journal of Organic Chemistry. 2020 (29): 4499–4509. doi:10.1002/ejoc.202000692. ISSN 1434-193X.
  61. Kräutler, Bernhard; Hörtensteiner, Stefan (2013). "139. Chlorophyll Breakdown – Chemistry, Biochemistry and Biology". In Kadish, Karl M.; Smith, Kevin M.; Guilard, Roger (eds.). Handbook of Porphyrin Science. Vol. 28. Singapore: World Scientific Publishing. p. 117–185.
  62. Beale, Samuel I. (1993). "Biosynthesis of phycobilins". Chemical Reviews. 93 (2): 785–802. doi:10.1021/cr00018a008. ISSN 0009-2665.
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