Bloodwood: the composition and secreting-site of the characteristic red exudate that gives the name to the Swartzia species (Fabaceae).
Anatomy
Bioactive potential
Latex
Laticifers
Phytochemistry
Secretory structure
Journal
Journal of plant research
ISSN: 1618-0860
Titre abrégé: J Plant Res
Pays: Japan
ID NLM: 9887853
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
21
08
2020
accepted:
15
12
2020
pubmed:
7
1
2021
medline:
23
1
2021
entrez:
6
1
2021
Statut:
ppublish
Résumé
The Swartzia species are commonly known as bloodwood due to the red exudate released from the stem after injury. This exudate has aroused great interest, and an integrative study is essential to describe it in detail. Thus, this work aimed to identify the red exudate's secreting-site in S. flaemingii and S. langsdorffii, and determine if it is a latex or a resin. Samples of the stem bark and the secondary xylem were prepared for histological analysis. Fresh exudates were dissolved in deuterated methanol and analyzed by
Identifiants
pubmed: 33403567
doi: 10.1007/s10265-020-01246-4
pii: 10.1007/s10265-020-01246-4
doi:
Substances chimiques
Antioxidants
0
Flavonoids
0
Latex
0
Plant Extracts
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
127-139Subventions
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 421121/2016-5
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 302806/2019-9
Organisme : Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
ID : E-23/203.026/2017
Organisme : Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
ID : E-26/202.752/2018
Références
Abdel-Kader MS, Bahler BD, Malone S, Werkhoven MC, Wisse JH, Neddermann KM, Bursuker I, Kingston DGI (2000) Bioactive Saponins from Swartzia schomburgkii from the Suriname Rainforest. J Nat Products 63:1461–1464
doi: 10.1021/np0000926
Alencar AC, Tölke ED, Mayer JLS (2020) New perspectives on secretory structures in Clusia (Clusiaceae–Clusiod clade): production of latex or resins? Botany 98:161–172
doi: 10.1139/cjb-2019-0103
Angyalossy V, Pace MR, Evert RF, Marcati CR, Oskolski AA, Terrazas T, Kotina E et al (2016) IAWA list of microscopic bark features. IAWA J 37:517–615
doi: 10.1163/22941932-20160151
APG [Angiosperm Phylogeny Group] IV (2016) An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants. Bot J Lin Soc 181:1–20
doi: 10.1111/boj.12385
Araujo MFD, Vieira IJC, Braz-Filho R, Vieira-da-Motta O, Mathias L (2009) Chemical constituents from Swartzia apetala Raddi var. glabra and evaluation of their antifungal activity against Candida spp. Rev Brasil Farmacog 19:366–369
doi: 10.1590/S0102-695X2009000300005
Badkhane Y, Yadav AS, Sharma AK, Raghuwanshi DK, Uikey SK, Mir FA, Lone SA, Murab T (2010) Pterocarpus marsupium Roxb-Biological activities and medicinal properties. Int J Adv Pharm Sci 1:350–357
Barbosa AC, Pace MR, Witovisk L, Angyalossy V (2010) A new method to obtain good anatomical slides of heterogeneous plant parts. IAWA J 31:373–383
doi: 10.1163/22941932-90000030
Benzie IF, Strain JJ (1996) The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem 239:70–76
pubmed: 8660627
doi: 10.1006/abio.1996.0292
Borel C, Gupta MP, Hostettmann K (1987) Molluscicidal saponins from Swartzia simplex. Phytochemistry 26:2685–2689
doi: 10.1016/S0031-9422(00)83572-4
Bukatsch F (1972) Bemerkungen zur doppelfärbung astrablau-safranin. Mikrokosmos 61:33–36
Calvano CD, Cataldi TRI, Kögel JF, Monopoli A, Palmisano F, Sundermeyer J (2017) Structural characterization of neutral saccharides by negative ion MALDI mass spectrometry using a superbasic proton sponge as deprotonating matrix. J Am Soc Mass Spectrometry 28:1666–1675
doi: 10.1007/s13361-017-1679-y
Chen K, Ríos JJ, Roca M, Pérez-Gálvez A (2015) Development of an accurate and high-throughput methodology for structural comprehension of chlorophylls derivatives. (II) Dephytylated derivatives. J Chromatogr A 1412:90–99
pubmed: 26277027
doi: 10.1016/j.chroma.2015.08.007
Costa GV, Costa HR, Santos RC, Melo-Filho AA, Chagas EA, Montero IF, Chaga PC, Melo AGR (2018) Bioactive Extracts from Swartzia latifolia. Chem Eng Trans 64:211–216
Croaker A, King GJ, Pyne JH, Anoopkumar-Dukie S, Liu L (2016) Sanguinaria canadensis: traditional medicine, phytochemical composition, biological activities and current uses. Int J Mol Sci 17:1–32
doi: 10.3390/ijms17091414
Dattoli LFF, Loto DE, Flores JR, Luque C, Debes M, Albornoz PL, Arias M (2011) Caracterización anatómica foliar de Lonchocarpus lilloi (Fabaceae, Papilionoideae). Lilloa 48:145–152
Dubois JL, Sneden AT (1995) Dihydrolicoisoflavone, a new isoflavanone from Swartzia polyphylla. J Nat Products 58:629–632
doi: 10.1021/np50118a028
Escobar JD, Prieto C, Pardo-Figuerez M, Lagaron JM (2018) Dragon’s blood sap: storage stability and antioxidant activity. Molecules 23:2641
pmcid: 6222551
doi: 10.3390/molecules23102641
Evert RF (2013) Anatomia das plantas de Esau: meristemas, células e tecidos do corpo da planta: sua estrutura, função e desenvolvimento, 3rd edn. Blucher, São Paulo
Fahn A (1979) Secretory tissues in plants. Academic Press, London
Fahn A (1990) Plant anatomy, 4th Edn. Butterworth Heinemann
Ferreira ICFR, Aires E, Barreira JCM, Estevinho LM (2009) Antioxidant activity of Portuguese honey samples: different contributions of the entire honey and phenolic extract. Food Chem 114:1438–1443
doi: 10.1016/j.foodchem.2008.11.028
Fischer UA, Carle R, Kammerer DR (2011) Identification and quantification of phenolic compounds from pomegranate (Punica granatum L.) peel, mesocarp, aril and differently produced juices by HPLC-DAD–ESI/MS
pubmed: 23140740
doi: 10.1016/j.foodchem.2010.12.156
Gerlach D (1984) Botanische Mikrotechnik: Eine Einführung. Thieme Verlag, Stuttgart
Güçlü-Üstündağ Ö, Mazza G (2007) Saponins: properties, applications and processing. Crit Rev Food Sci Nutr 47:231–258
pubmed: 17453922
doi: 10.1080/10408390600698197
Gupta D (2011) Phytochemical investigation and pharmacological evaluation of medicinal plants for anti-microbial, anti-oxidant, anti-inflammatory activities and nephrotoxicity. Dissertation, University School of Biotechnology
Hamdani AM, Wani IA, Bhat NA, Masoodi FA (2018) Chemical composition, total phenolic content, antioxidant and antinutritional characterization of exudate gums. Food Biosci 23:67–74
doi: 10.1016/j.fbio.2018.03.006
Hernandez-Hernandez AB, Alarcon-Aguilar FJ, Almanza-Perez JC, Nieto-Yañez O, Olivares-Sanchez JM, Duran-Diaz A, Rodriguez-Monroy MA, Canales-Martinez MM (2017) Antimicrobial and anti-inflammatory activities, wound-healing effectiveness and chemical characterization of the latex of Jatropha neopauciflora Pax. J Ethnopharmacol 204:1–7
pubmed: 28392457
doi: 10.1016/j.jep.2017.04.003
Hussain M, Debnath B, Qasim M, Bamisile BS, Islam W, Hameed MS, Wang L, Qiu D (2019) Role of saponins in plant defense against specialist herbivores. Molecules 24:2067
pmcid: 6600540
doi: 10.3390/molecules24112067
Jin J, Lao J, Zhou R, He W, Qin Y, Zhong C, Xie J, Liu H, Wan D, Zhang S, Qin Y (2018) Simultaneous identification and dynamic analysis of saccharides during steam processing of rhizomes of Polygonatum cyrtonema by HPLC–QTOF–MS/MS. Molecules 23:2855
pmcid: 6278431
doi: 10.3390/molecules23112855
Johansen DA (1940) Plant microtechnique. McGraw-Hill, New York
Jura-Morawiec J, Tulik M (2015) Morpho-anatomical basis of dragon’s blood secretion in Dracaena draco stem. Flora-Morph, Distr, Funct Ecol Plants 213:1–5
Jura-Morawiec J, Tulik M (2016) Dragon’s blood secretion and its ecological significance. Chemoecology 26:101–105
pubmed: 27239099
pmcid: 4863904
doi: 10.1007/s00049-016-0212-2
Kamarulzaman FA, Shaari K, Ho ASH, Lajis NH, Teo SH, Lee HB (2011) Derivatives of Pheophorbide-a and Pheophorbide-b from Photocytotoxic Piper penangense extract. Chem Biodiv 8:494–502
doi: 10.1002/cbdv.201000341
Khan S, Nazir M, Raiz N, Saleem M, Zengin G, Fazal G, Saleem H, Mukhtar M, Tousif MI, Tareen RB, Abdallah HH, Mahomoodally FM (2019) Phytochemical profiling, in vitro biological properties and in silico studies on Caragana ambigua stocks (Fabaceae): a comprehensive approach. Ind Crops Products 131:117–124
doi: 10.1016/j.indcrop.2019.01.044
Konno K (2011) Plant latex and other exudates as plant defense systems: roles of various defense chemicals and proteins contained therein. Phytochemistry 72:1510–1530
pubmed: 21450319
doi: 10.1016/j.phytochem.2011.02.016
Langenheim JH (2003) Plant resins: chemistry, evolution, ecology, and ethnobotany. Timber Press, Oregon
Lewinsohn TM (1991) The geographical distribution of plant latex. Chemoecology 2:64–68
doi: 10.1007/BF01240668
Lewis G, Schrire B, Mackinder B, Lock M (2005) Legumes of the World. Royal Botanic Gardens, Kew, Richmond
Li S, Lin Z, Jiang H, Tong L, Wang H, Chen S (2016) Rapid identification and assignation of the active ingredients in fufang banbianlian injection using HPLC-DAD-ESI-IT-TOF-MS. J Chrom Sci 54:1225–1237
doi: 10.1093/chromsci/bmw055
Licá ICL, Soares AMS, Mesquita LSS, Malik S (2018) Biological properties and pharmacological potential of plant exudates. Food Res Int 105:1039–1053
pubmed: 29433195
doi: 10.1016/j.foodres.2017.11.051
Llorent-Martínez EJ, Ortega-Barrales P, Zengin G, Uysal S, Ceylan R, Guler GO, Mocane A, Aktumsek A (2016) Lathyrus aureus and Lathyrus pratensis: characterization of phytochemical profiles by liquid chromatography-mass spectrometry, and evaluation of their enzyme inhibitory and antioxidant activities. Royal Soc Chem Adv 6:88996–89006
LPWG [Legume Phylogeny Working Group] (2013) Legume phylogeny and classification in the 21st century: progress, prospects and lessons for other species-rich clades. Taxon 62:217–248
doi: 10.12705/622.8
LPWG [Legume Phylogeny Working Group] (2017) A new subfamily classification of the Leguminosae based on a taxonomically comprehensive phylogeny. Taxon 66:44–77
doi: 10.12705/661.3
Magalhães AF, Tozzi AMGA, Santos CC, Serrano DR, Zanotti-Magalhães EM, Magalhães EG, Magalhães LA (2003) Saponins from Swartzia langsdorffii: biological Activities. Memórias do Instituto Oswaldo Cruz 98:713–718
pubmed: 12973543
doi: 10.1590/S0074-02762003000500022
Mahlberg PG (1993) Laticifers: an historical perspective. Bot Rev 59:1–23
doi: 10.1007/BF02856611
Marqui SR, Lemos RB, Santos LA, Castro-Gamboa I, Cavalheiro AJ, Bolzani VS, Silva DHS, Scorzoni L, Fusco-Almeida AM, Mendes-Giannini MJS, Young MCM, Torres LMB (2008) Antifungal saponins from Swartzia langsdorffii. Quim Nova 31:828–831
doi: 10.1590/S0100-40422008000400023
Meda A, Lamien CE, Romito M, Millogo J, Nacoulma OG (2005) Determination of the total phenolic, flavonoid and proline contents in Burkina Fasan honey, as well as their radical scavenging activity. Food Chem 91:571–577
doi: 10.1016/j.foodchem.2004.10.006
Mena P, Calani L, Dall’Asta C, Galaverna G, García-Viguera C, Bruni R, Crozier A, Del Rio D (2012) Rapid and Comprehensive Evaluation of (Poly)phenolic Compounds in Pomegranate (Punica granatum L.) Juice by UHPLC-MS
pubmed: 23519255
pmcid: 6268091
doi: 10.3390/molecules171214821
Milenković SM, Zvezdanović JB, Anđelković TD, Marković DZ (2012) The identification of chlorophyll and its derivatives in the pigment mixtures: HPLC-chromatography, visible and mass spectroscopy studies. Adv Technol 1:16–24
Moses T, Papadopoulou KK, Osbourn A (2014) Metabolic and functional diversity of saponins, biosynthetic intermediates and semi-synthetic derivatives. Crit Rev Biochem Mol Biol 49:439–462
pubmed: 25286183
pmcid: 4266039
doi: 10.3109/10409238.2014.953628
O’Brien TP, Feder N, McCully ME (1964) Polychromatic staining of plant cell walls by toluidine blue O. Protoplasma 59:368–373
doi: 10.1007/BF01248568
Osawa K, Yasuda H, Maruyamma T, Morita H, Takeya K, Itokawa H (1992) Isoflavones from the heartwood of Swartzia polyphylla and their antibacterial activity against cariogenic bacteria. Chem Pharm Bull 40:2970–2974
doi: 10.1248/cpb.40.2970
Oszmianski J, Kolniak-Ostek J, Lachowicz S, Gorzelany J, Matłok N (2017) Phytochemical compounds and antioxidant activity in different cultivars of cranberry (Vaccinium macrocarpon L). J Food Sci 82:2569–2575
pubmed: 28973819
doi: 10.1111/1750-3841.13924
Pedersoli GD, Leme FM, Leite VG, Teixeira SP (2019) Anatomy solves the puzzle of explosive pollen release in wind-pollinated urticalean rosids. Am J Bot 106:489–506
pubmed: 30875436
doi: 10.1002/ajb2.1254
Pickard WF (2008) Laticifers and secretory ducts: two other tube systems in plants. New Phytol 177:877–888
pubmed: 18086227
doi: 10.1111/j.1469-8137.2007.02323.x
Pinto RB (2013) Estudos citogenéticos e taxonômicos em espécies brasileiras de Swartzia Schreb. (Leguminosae-Papilionoideae). Dissertation. Universidade Estadual de Campinas
Pollier J, Morreel K, Geelen D, Goossens A (2011) Metabolite profiling of triterpene saponins in Medicago truncatula hairy roots by liquid chromatography fourier transform ion cyclotron resonance mass spectrometry. J Nat Prod 74:1462–1476
pubmed: 21615146
doi: 10.1021/np200218r
Prado E, Demarco D (2018) Laticifers and secretory ducts: similarities and differences. In: Hufnagel L (ed) Ecosystem services and global ecology. IntechOpen, London, pp 103–123
Ramos MV, Freitas CDT, Morais FS, Prado E, Medina MC, Demarco D (2020) Plant latex and latex-borne defense. In: Nawrot R (ed) Advances in botanical research: Latex, laticifers and their molecular components: From Functions to Possible Applications, vol 93. Academic Press, London, pp 1–25
doi: 10.1016/bs.abr.2019.09.002
Rojas R, Bustamante B, Ventosilla P, Fernadez I, Caviedes L, Gilman RH, Lock O, Hammond GB (2006) Larvicidal, antimicobacterial and antifungal compounds from the bark of the Peruvian plant Swartzia polyphylla DC. Chem Pharm Bull 54:278–279
doi: 10.1248/cpb.54.278
Sanchez CS, Rocha AFI, Pinheiro MLB, Andrade CHS, Monte FJQ (1999) Brachyrachisina: isoflavonainedita de Swartzia (Leguminosae). Acta Amazonica 29:419–422
doi: 10.1590/1809-43921999293422
Santos RC, Melo Filho AAD (2013) Fitoquímica e Atividade Biológica do Gênero Swartzia: Uma Revisão. Orbital-Electron J Chem 5:143–147
Silva MJ, Tozzi AMGA, Lewis GP (2010) Two new species of Lonchocarpus (Leguminosae, Papilionoideae, Millettieae) from Brazil. Kew Bull 65:29–35
doi: 10.1007/s12225-009-9170-y
Sousa MM, Melo MJ, Parola AJ, Melo SS, Catarino F, Pina F, Cook FEM, Simmonds MSJ, Lopes JA (2008) Flavylium chromophores as species markers for dragon’s blood resins from Dracaena and Daemonorops trees. J Chromato A 1209:153–161
doi: 10.1016/j.chroma.2008.09.007
Stefano V, Pitonzo R, Schillaci D (2014) Phytochemical and anti-staphylococcal biofilm assessment of Dracaena draco L. spp. draco resin. Pharm Mag 10:434–440
doi: 10.4103/0973-1296.133300
Teixeira SP, Marinho CR, Leme FM (2020) Structural diversity and distribution of laticifers. In: Nawrot R (ed) Advances in botanical research: latex, laticifers and their molecular components: from functions to possible applications, vol 93. Academic Press, London, pp 27–49
doi: 10.1016/bs.abr.2019.09.003
Torke BM, Mansano VF (2009) A phylogenetically based sectional classification of Swartzia (Leguminosae-Papilionoideae). Taxon 58:913–924
doi: 10.1002/tax.583019
Torke BM, Schaal BA (2008) Molecular phylogenetics of the species-rich neotropical genus Swartzia (Leguminosae, Papilionoideae) and related genera of the Swartzioid clade. Am J Bot 95:215–228
pubmed: 21632346
doi: 10.3732/ajb.95.2.215
Treutter D (2006) Significance of flavonoids in plant resistance: a review. Environ Chem Lett 4:147–157
doi: 10.1007/s10311-006-0068-8
Triana-Gómez MA, Roso GG, Posso SDP (2008) Estudio de las propiedades mecánicas de la madera de palosangre (Brosimum rubescens Taub.), procedencia: Leticia. Amazonas. Colombia Forestal 11:149–164
doi: 10.14483/udistrital.jour.colomb.for.2008.1.a10
Vasile FE, Romero AM, Judis MA, Mattalloni M, Virgolini MB, Mazzobre MF (2019) Phenolics composition, antioxidant properties and toxicological assessment of Prosopis alba exudate gum. Food Chem 285:369–379
pubmed: 30797359
doi: 10.1016/j.foodchem.2019.02.003
Védékoi J, Selestin SD, Abdoulaye H, Justin K, Djamilah Z, Pierre K (2019) Investigation of antioxidant activity of the ethanol extract of the resin exudates of trunk bark of Boswellia dalzielii Hutch (Burseraceae). J Mater Environ Sci 10:1413–1419
Verardo G, Duse I, Callea A (2009) Analysis of underivatized oligosaccharides by liquid chromatography/electrospray ionization tandem mass spectrometry with post-column addition of formic acid. Rapid Commun Mass Spectr 23:1607–1618
doi: 10.1002/rcm.4047
Viera I, Roca M, Pérez-Gálvez A (2018) Mass spectrometry of non-allomerized chlorophylls a and b derivatives from plants. Curr Organic Chem 22:842–876
doi: 10.2174/1385272821666170920164836
Warowicka A, Nawrot R, Goździcka-Józefiak A (2020) Pharmacologically active compounds from latex-bearing plants. In: Nawrot R (ed] Advances in botanical research: latex, laticifers and their molecular components: from functions to possible applications, vol. 93, Academic Press, London, pp 119–151
Weaver PL (1997) Pterocarpus officinalis Jacq. Bloodwood Leguminosae, Legume Family, lotoideae, Pea Subfamily. SO-ITF-SM-87
Wiedenhoeft AC, Riina R, Berry PE (2009) “Ray-Intrusive” laticifers in species of Croton section Cyclostigma (Euphorbiaceae). IAWA J 30:135–148
doi: 10.1163/22941932-90000209
Zerbib M, Mazauric JP, Meudec E, Le Guernevé C, Lepak A, Nidetzky B, Cheynier V, Terrier N, Saucier C (2018) New flavanol O-glycosides in grape and wine. Food Chem 266:441–448
pubmed: 30381210
doi: 10.1016/j.foodchem.2018.06.019
Zvezdanović JB, Petrović SM, Marković DZ, Andjelković TD, Andjelković DH (2014) Electrospray ionization mass spectrometry combined with ultra high performance liquid chromatography in the analysis of in vitro formation of chlorophyll complexes with copper and zinc. J Serbian Chem Soc 79:689–706
doi: 10.2298/JSC130918009Z