Skip to main content

Prosopis juliflora: Phytochemical, Toxicological, and Allelochemicals

  • Living reference work entry
  • First Online:
Co-Evolution of Secondary Metabolites

Abstract

Prosopis juliflora (Fabaceae), which is also known as mesquite, is particularly invasive in exotic environments and has become one of the world’s 100 most invasive species that is globally distributed. This scenario is mainly due to the allelochemicals released by its roots, leaves, and fruits that inhibit seed germination of neighboring species. Therefore, ecosystem-level changes create monospecific stands and impair the chemistry and biophysical properties of soil. The metabolites from Prosopis juliflora with allelopathic properties result from two major biosynthetic pathways: shikimic acid metabolites and piperidine alkaloids. Several Prosopis species have substantial impacts on biodiversity, ecosystem services, and local and regional economies in their native terrain; others provide multiple benefits to local communities. Overall, P. juliflora has demonstrated to be a versatile raw material, widely applicable in the food, cosmetic, pharmaceutical, agricultural, and renewable energy industries, providing progress in several fields of science and technology.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Institutional subscriptions

References

  1. Walling LL (2000) The myriad plant responses to herbivores. Plant Growth Regul 19:195–216

    CAS  Google Scholar 

  2. Haig T (2008) Allelochemicals in plants. Springer, New York

    Book  Google Scholar 

  3. Bennett RN, Wallsgrove RM (1994) Secondary metabolites in plant defense-mechanisms. New Phytol 127:617–633

    Article  CAS  PubMed  Google Scholar 

  4. Kessler A, Baldwin IT (2002) Plant responses to insect herbivory: the emerging molecular analysis. Annu Rev Plant Biol 53:299–328

    Article  CAS  PubMed  Google Scholar 

  5. Wu JQ, Baldwin IT (2009) Herbivory-induced signalling in plants: perception and action. Plant Cell Environ 32:1161–1174

    Article  CAS  PubMed  Google Scholar 

  6. Cheng F, Cheng ZH (2015) Research progress on the use of plant allelopathy in agriculture and the physiological and ecological mechanisms of allelopathy. Front Plant Sci 6:1–16

    CAS  Google Scholar 

  7. Singh HP, Batish DR, Kohli RK (2003) Allelopathic interactions and allelochemicals: new possibilities for sustainable weed management. CRC Crit Rev Plant Sci 22:239–311

    Article  CAS  Google Scholar 

  8. Callaway R, Ridenour WM (2004) Novel weapons: invasive success and the evolution of increased competitive ability. Front Ecol Environ 2:436–443

    Article  Google Scholar 

  9. Vivanco JM, Bais HP, Stermitz FR, Thelen G, Callaway R (2004) Biogeographical variation in community response to root allelochemistry: novel weapons and exotic invasion. Ecol Lett 7:285–292

    Article  Google Scholar 

  10. Ridenour WM, Callaway R (2001) The relative importance of allelopathy in interference: the effects of an invasive weed on a native bunchgrass. Oecologia 126:444–450

    Article  PubMed  Google Scholar 

  11. He W-M, Feng Y, M Ridenour W, Thelen G, Pollock J, Diaconu A, Callaway RM (2009) Novel weapons and invasion: biogeographic differences in the competitive effects of Centaurea maculosa and its root exudate (±)-catechin. Oecologia 159:803–815

    Article  PubMed  Google Scholar 

  12. Burkart A (1976) A monograph of the genus Prosopis (Leguminosae, subfam. Mimosoidae). J Arnold Arbor 57:219–249

    Google Scholar 

  13. Walter K Prosopis, an alien among the sacred trees of South India. Dissertation, University of Helsinki

    Google Scholar 

  14. Nascimento CES, Tabarelli M, Silva C, Leal I, Tavares W, Serrão J, Zanuncio J (2014) The introduced tree Prosopis juliflora is a serious threat to native species of the Brazilian Caatinga vegetation. Sci Total Environ 481:108–113

    Article  CAS  Google Scholar 

  15. Oliveira BF, Costa GC, Fonseca CR (2018) Niche dynamics of two cryptic Prosopis invading South American drylands. Biol Invasions 20:181–194

    Article  Google Scholar 

  16. Resumo L, Cunha L, Ramonildes A (2012) A Trajetória da Algaroba no Semiárido Nordestino: Dilemas Políticos e Científicos. Raízes 32:72–95

    Google Scholar 

  17. Rodrigues LC, AAd S, RBd S, AFMd O, LdHC A (2013) Conhecimento e uso da carnaúba e da algaroba em comunidades do Sertão do Rio Grande do Norte, Nordeste do Brasil. Revista Árvore 37:451–457

    Article  Google Scholar 

  18. UPd A, LdHC A (2002) Conhecimento botânico tradicional e conservação em uma área de caatinga no estado de Pernambuco, Nordeste do Brasil. Acta Bot Bras 16:273–285

    Article  Google Scholar 

  19. de Albuquerque UP, de Medeiros PM, de Almeida ALS, Monteiro JM, de Freitas Lins Neto EM, de Melo JG, dos Santos JP (2007) Medicinal plants of the caatinga (semi-arid) vegetation of NE Brazil: a quantitative approach. J Ethnopharmacol 114:325–354

    Article  PubMed  Google Scholar 

  20. Braga R (1976) Plantas do Nordeste, especialmente do Ceará. Universitária-UFRN, Natal

    Google Scholar 

  21. Queiroz L (2009) Leguminosas da caatinga. Editora Universitária UEFS, Feira de Santana

    Google Scholar 

  22. Mendes B (1989) Potencialidades de Utilização da Algarobeira (Prosopis juliflora (SW) DC) no Semi-árido Brasileiro. Coleção Mossoroense, Mossoró

    Google Scholar 

  23. Shackleton R, Le Maitre D, Pasiecznik N, Richardson D (2014) Prosopis: a global assessment of the biogeography, benefits, impacts and management of one of the world’s worst woody invasive plant taxa. AoB Plants 6:1–18

    Article  Google Scholar 

  24. Patnaik P, Abbasi T, Abbasi SA (2017) Prosopis (Prosopis juliflora): blessing and bane. J Trop Ecol 58:455–483

    Google Scholar 

  25. Green TR, Ryan CA (1972) Wound-induced proteinase inhibitor in plant leaves – possible defense mechanims against insects. Science 175:776–777

    Article  CAS  PubMed  Google Scholar 

  26. Gatehouse JA (2002) Plant resistance towards insect herbivores: a dynamic interaction. New Phytol 156:145–169

    Article  CAS  PubMed  Google Scholar 

  27. Tian D, Traw MB, Chen JQ, Kreitman M, Bergelson J (2003) Fitness costs of R-gene-mediated resistance in Arabidopsis thaliana. Nature 423:74–77

    Article  CAS  PubMed  Google Scholar 

  28. Zavala JA, Patankar AG, Gase K, Baldwin IT (2004) Constitutive and inducible trypsin proteinase inhibitor production incurs large fitness costs in Nicotiana attenuata. Proc Natl Acad Sci U S A 101:1607–1612

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Howe GA, Jander G (2008) Plant immunity to insect herbivores. Annu Rev Plant Biol 59:41–66

    Article  CAS  PubMed  Google Scholar 

  30. Ibrahim M, Nadir M, Ali A, Ahmad VU, Rasheed M (2013) Phytochemical analyses of Prosopis juliflora Swartz DC. Pak J Bot 45:2101–2104

    CAS  Google Scholar 

  31. Aqeel A, Khursheed AK, Viqaruddin A, Sabiha Q (1989) Antimicrobial activity of julifloricine isolated from Prosopis juliflora. Arzneimittelforschung 39:652–655

    CAS  PubMed  Google Scholar 

  32. Ahmad V, Basha A, Haque W (1978) New alkaloids from Prosopis juliflora DC. Z Naturforschung 33:347–348

    Article  Google Scholar 

  33. Ahmad A, Khursheed A, Sabiha Q, Viqaruddin A (1989) Antifungal activity of some hydrosoluble Prosopis juliflora alkaloids. Fitoterapia 60:86–89

    CAS  Google Scholar 

  34. Nakano H, Nakajima E, Hiradate S, Fujii Y, Yamada K, Shigemori H, Hasegawa K (2004) Growth inhibitory alkaloids from mesquite (Prosopis juliflora (Sw.) DC.) leaves. Phytochemistry 65:587–591

    Article  CAS  PubMed  Google Scholar 

  35. Sirmah P, Dumarçay S, Masson E, Gérardin P (2009) Unusual amount of (−)-mesquitol from the heartwood of Prosopis juliflora. Nat Prod Res 23:183–189

    Article  CAS  PubMed  Google Scholar 

  36. Chellamuthu V, Balasusbramanian TN, Rajarajan A, Palaniappan SP (1997) Allelopathic influence of Prosopis juliflora (Swartz) DC. on field crops. Allelopathy J 4:291–302

    Google Scholar 

  37. Abbasi T, Abbasi SA (2011) Sources of pollution in rooftop rainwater harvesting systems and their control. Crit Rev Environ Sci Technol 41:2097–2167

    Article  Google Scholar 

  38. Nakano H, Fujii Y, Suzuki T, Yamada K, Kosemura S, Yamamura S, Suzuki T, Hasegawa K (2001) A growth-inhibitory substance exuded from freeze-dried mesquite (Prosopis juliflora (Sw.) DC.) leaves. Plant Growth Regul 33:165–168

    Article  CAS  Google Scholar 

  39. Nakano H, Fujii Y, Yamada K, Kosemura S, Yamamura S, Hasegawa K, Suzuki T (2002) Isolation and identification of plant growth inhibitors as candidate(s) for allelopathic substance(s), from aqueous leachate from mesquite (Prosopis juliflora (Sw.) DC.) leaves. Plant Growth Regul 37:113–117

    Article  CAS  Google Scholar 

  40. Nakano H, Nakajima E, Fujii Y, Yamada K, Shigemori H, Hasegawa K (2003) Leaching of the allelopathic substance, L-tryptophan from the foliage of mesquite (Prosopis juliflora (Sw.) DC.) plants by water spraying. Plant Growth Regul 40:49–52

    Article  CAS  Google Scholar 

  41. Dewick PM (2002) Medicinal natural products: a biosynthetic approach. Wiley, Great Britain

    Google Scholar 

  42. Wink M, Schimmer O (2010) Molecular modes of action of defensive secondary metabolites, vol 2. Wiley-Blackwell, Chichester

    Google Scholar 

  43. Wink M (2003) Evolution of secondary metabolites from an ecological and molecular phylogenetic perspective. Phytochemistry 64:3–19

    Article  CAS  PubMed  Google Scholar 

  44. William K, Jafri L (2015) Mesquite (Prosopis juliflora): livestock grazing, its toxicity and management. Bioresour Technol 2:49–58

    Google Scholar 

  45. Inderjit STR, Callaway RM, Pollock JL, Kaur J (2008) Allelopathy and plant invasions: traditional, congeneric, and bio-geographical approaches. Biol Invasions 10:875–890

    Article  Google Scholar 

  46. Siddiqui S, Bhardwaj S, Saeed Khan S, Kumar Meghvanshi M (2009) Allelopathic effect of different concentration of water extract of Prosopsis juliflora leaf on seed germination and radicle length of wheat (Triticum aestivum Var-Lok-1). Am-Eurasian J Sci Res 4:81–84

    Google Scholar 

  47. Cavalcante GM, Moreira AFC, Vasconcelos SD (2006) Potencialidade inseticida de extratos aquosos de essências florestais sobre mosca-branca. Pesqui Agropecu Bras 41:9–14

    Article  Google Scholar 

  48. Raghavendra MP, Satish S, Raveesha KA (2009) Alkaloid extracts of Prosopis juliflora (Sw.) DC. (Mimosaceae) against Alternaria alternata. J Biopest 2:56–59

    CAS  Google Scholar 

  49. Ikram N, Dawar S (2013) Effect of Prosopis juliflora (Sw.) DC. in the control of root rot fungi of cowpea (Vigna Unguiculata L.) and mung bean [Vigna Radiata (L.) Wilczek]. Pak J Bot 45:649–654

    Google Scholar 

  50. Hughes JB, Sousa JS, Barreto RA, Silva AR, Souza CS, Silva VDA, Silva BMP, Freitas SRVB, Costa MFD, EL-Bacha RS, Batatinha MJM, Tardy M, Velozo ES, Costa SL (2005) Cytotoxic effects of an extract containing alkaloids obtained from Prosopis juliflora Sw. D.C. (Algaroba) pods on glioblastoma cells. Rev Bras Saúde Prod Anim 6:31–41

    Google Scholar 

  51. Silva AMM, Silva AR, Pinheiro AM, Freitas SRVB, Silva VDA, Souza CS, Hughes JB, El-Bachá RS, Costa MFD, Velozo ES, Tardy M, Costa SL (2007) Alkaloids from Prosopis juliflora leaves induce glial activation, cytotoxicity and stimulate NO production. Toxicon 49:601–614

    Article  CAS  PubMed  Google Scholar 

  52. Damasceno GAD, Ferrari M, Giordani RB (2017) Prosopis juliflora (SW) DC, an invasive specie at the Brazilian Caatinga: phytochemical, pharmacological, toxicological and technological overview. Phytochem Rev 16:309–331

    Article  CAS  Google Scholar 

  53. Henciya S, Seturaman P, James AR, Tsai Y-H, Nikam R, Wu Y-C, Dahms H-U, Chang FR (2017) Biopharmaceutical potentials of Prosopis spp. (Mimosaceae, Leguminosa). J Food Drug Anal 25:187–196

    Article  CAS  PubMed  Google Scholar 

  54. Singh S, Verma SK (2012) Study of the distribution profile of piperidine alkaloids in various parts of Prosopis juliflora by the application of Direct Analysis in Real Time Mass Spectrometry (DART-MS). Nat Prod Bioprospect 2:206–209

    Article  CAS  PubMed Central  Google Scholar 

  55. Singh S (2012) Phytochemical analysis of different parts of Prosopis juliflora. Int J Curr Pharm Res 4:59–61

    Google Scholar 

  56. Nakano H, Nakajima E, Fujii Y, Shigemori H, Hasegawa K (2004) Structure-activity relationships of alkaloids from mesquite (Prosopis juliflora (Sw.) DC.). Plant Growth Regul 44:207–210

    Article  CAS  Google Scholar 

  57. Bazie S, Ayalew A, Woldetsadik K (2014) Antifungal activity of some plant extracts against (Colletotrichum Musae) the cause of Postharvest Banana Anthracnose. J Plant Pathol Microbiol 5:2–5

    Google Scholar 

  58. Rincón F, Muñoz J, Ramírez P, Galán H, Alfaro MC (2014) Physicochemical and rheological characterization of Prosopis juliflora seed gum aqueous dispersions. Food Hydrocoll 35:348–357

    Article  CAS  Google Scholar 

  59. Sharmila S, Rebecca Jeyanthi L, Saduzzaman M (2013) Biodegradation of tannery effluent using Prosopis juliflora. Int J ChemTech Res 5:2186–2192

    CAS  Google Scholar 

  60. Inderjit (1996) Plant phenolics in allelopathy. Bot Rev 62:186–202

    Article  Google Scholar 

  61. Li Z-H, Wang Q, Ruan X, Pan C-D, Jiang D-A (2010) Phenolics and plant allelopathy. Molecules 15:8933

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Azero EG, Andrade CT (2002) Testing procedures for galactomannan purification. Polym Test 21:551–556

    Article  CAS  Google Scholar 

  63. Azero EG, Andrade CT (2006) Characterisation of Prosopis juliflora seed gum and the effect of its addition to k-carrageenan systems. J Braz Chem Soc 17:844–850

    Article  CAS  Google Scholar 

  64. Bhatia H (2013) Linkage analysis in an nonasaccharide from Prosopis juliflora by methylation, periodate oxidation and NMR studies. Int J Pharmtech Res 5:1530–1537

    CAS  Google Scholar 

  65. Bhatia H, Gupta PK, Soni PL (2014) Structure of the oligosaccharides isolated from Prosopis juliflora (Sw.) DC. seed polysaccharide. Carbohydr Polym 101:438–443

    Article  CAS  PubMed  Google Scholar 

  66. López-Franco YL, Cervantes-Montaño CI, Martínez-Robinson KG, Lizardi-Mendoza J, Robles-Ozuna LE (2013) Physicochemical characterization and functional properties of galactomannans from mesquite seeds (Prosopis spp.). Food Hydrocoll 30:656–660

    Article  CAS  Google Scholar 

  67. Vieira ÍGP, Mendes FNP, Gallão MI, de Brito ES (2007) NMR study of galactomannans from the seeds of mesquite tree (Prosopis juliflora (Sw) DC). Food Chem 101:70–73

    Article  CAS  Google Scholar 

  68. Dore CMPG, Faustino Alves MGC, LSE PW, Costa TG, Sabry DA, de Souza Rêgo LAR, Accardo CM, HAO R, LGA F, Leite EL (2013) A sulfated polysaccharide, fucans, isolated from brown algae Sargassum vulgare with anticoagulant, antithrombotic, antioxidant and anti-inflammatory effects. Carbohydr Polym 91:467–475

    Article  CAS  PubMed  Google Scholar 

  69. Hedin PA, McCarty JC, Dollar DA (1997) Effects of foliar applications of carbohydrates on the yield of cotton (Gossypium hirsutum) lint. J Agric Food Chem 45:2763–2767

    Article  CAS  Google Scholar 

  70. Goel U, Saxena DB, Kumar B (1989) Comparative study of allelopathy as exhibited by Prosopis juliflora swartz and Prosopis cineraria (L) druce. J Chem Ecol 15:591–600

    Article  CAS  PubMed  Google Scholar 

  71. Warrag MOA (1994) Autotoxicity of mesquite (Prosopis juliflora) pericarps on seed germination and seedling growth. J Arid Environ 27:79–84

    Article  Google Scholar 

  72. Al-Humaid AI, Warrag MOA (1998) Allelopathic effects of mesquite (Prosopis juliflora) foliage on seed germination and seedling growth of bermudagrass (Cynodon dactylon). J Arid Environ 38:237–243

    Article  Google Scholar 

  73. Getachew S, Demissew S, Woldemariam T (2012) Allelopathic effects of the invasive Prosopis juliflora (Sw.) DC. on selected native plant species in middle Awash, Southern Afar Rift of Ethiopia. Manag Biol Invasion 3:105–114

    Article  Google Scholar 

  74. Kaur R, Callaway RM, Inderjit (2014) Soils and the conditional allelopathic effects of a tropical invader. Soil Biol Biochem 78:316–325

    Article  CAS  Google Scholar 

  75. Tian G, Bi Y, Sun Z, Zhang L (2015) Phenolic acids in the plow layer soil of strawberry fields and their effects on the occurrence of strawberry anthracnose. Eur J Plant Pathol 143:581–594

    Article  CAS  Google Scholar 

  76. Inderjit I, Mallik AU (1996) The nature of interference potential of Kalmiaangustifolia. Can J For Res 26:1899–1904

    Article  Google Scholar 

  77. Fries LLM, Pacovsky RS, Safir GR, Siqueira JO (1997) Plant growth and Arbuscular Mycorrhizal fungal colonization affected by exogenously applied phenolic compounds. J Chem Ecol 23:1755–1767

    Article  CAS  Google Scholar 

  78. Zribi I, Omezzine F, Haouala R (2014) Variation in phytochemical constituents and allelopathic potential of Nigella sativa with developmental stages. S Afr J Bot 94:255–262

    Article  CAS  Google Scholar 

  79. Djurdjević L, Gajić G, Kostić O, Jarić S, Pavlović M, Mitrović M, Pavlović P (2012) Seasonal dynamics of allelopathically significant phenolic compounds in globally successful invader Conyza canadensis L. plants and associated sandy soil. Flora 207:812–820

    Article  Google Scholar 

  80. Kaur R, Gonzáles WL, Llambi LD, Soriano PJ, Callaway RM, Rout ME, Gallaher TJ, Inderjit (2012) Community impacts of Prosopis juliflora invasion: biogeographic and congeneric comparisons. PLoS One 7:e44966

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  81. Shah RH, Baloch MS, Khan AA, Ijaz M, Zubair M (2018) Bioherbicidal assessment of aqueous extracts of Mesquite (Prosopis juliflora) on weeds control and growth, yield and quality of wheat. Planta Daninha 36:1–13

    Article  Google Scholar 

  82. Abdulahi MM, Abdulkerim J (2017) Prosopis Juliflora L: distribution, impacts, causes and alternative control methods in Ethiopia. Trop Subtrop Agroecosystems 20:75–89

    Google Scholar 

  83. Bartlett D, Milliken S, Parmar D (2018) Prosopis for prosperity’: using an invasive non-native shrub to benefit rural livelihoods in India. Curr Sci 114:2142–2146

    Google Scholar 

  84. Choge SK, Pasiecznik NM, Harvey M, Wright J, Awan SZ, Harris PJC (2007) Prosopis pods as human food, with special reference to Kenya. Water SA 33:419–424

    CAS  Google Scholar 

  85. Wise RM, van Wilgen BW, Le Maitre DC (2012) Costs, benefits and management options for an invasive alien tree species: the case of mesquite in the Northern Cape, South Africa. J Arid Environ 84:80–90

    Article  Google Scholar 

  86. Walter KJ, Armstrong KV (2014) Benefits, threats and potential of Prosopis in South India, vol 23, pp 232–247

    Google Scholar 

  87. Manhique AJ, King’ori AM, Wachira AM (2017) Effect of ground mature prosopis (Prosopis juliflora) pods inclusion in layer diets on performance of improved indigenous chicken in Kenya. Livest Res Rural Dev 29:19

    Google Scholar 

  88. Tabosa IM, Quintans-Júnior LJ, Pamplona FV, Almeida RN, EVLd C, MSd S, Souza JCA, Barbosa Filho JM (2000) Isolamento biomonitorado de alcalóides tóxicos de Prosopis juliflora (algaroba). Rev bras farmacogn 9–10:11–22

    Google Scholar 

  89. Dhivya K, Vengateswari G, Arunthirumeni M, Karthi S, Senthil-Nathan S, Shivakumar MS (2018) Bioprospecting of Prosopis juliflora (Sw.) DC seed pod extract effect on antioxidant and immune system of Spodoptera litura (Lepidoptera: Noctuidae). Physiol Mol Plant Pathol 101:45–53

    Article  CAS  Google Scholar 

  90. Bansal SK, Singh KV, Sharma S, Sherwani MRK (2012) Laboratory observations on the larvicidal efficacy of three plant species against mosquito vectors of malaria, Dengue/Dengue Hemorrhagic Fever (DF/DHF) and lymphatic filariasis in the semi-arid desert. J Environ Biol 33:617–621

    CAS  PubMed  Google Scholar 

  91. Yadav R, Tyagi V, Tikar SN, Sharma AK, Mendki MJ, Jain AK, Sukumaran D (2014) Differential larval toxicity and oviposition altering activity of some indigenous plant extracts against dengue and chikungunya vector Aedes albopictus. J Arthropod-Borne Di 8:174–185

    Google Scholar 

  92. Dubow J (2011) Still-life, after-life, nature morte: W.G. Sebald and the demands of landscape. Routledge, London

    Google Scholar 

  93. Dave PN, Bhandari J (2013) Prosopis Julifora: a review. Int J Chem Stud 1:181–196

    Google Scholar 

  94. Carter EJV, Sherman P (1980) Rheological properties and applications of Mesquite tree (Prosopis Juliflora) gum 2. Rheological properties and stability of O/W emulsions containing Mesquite gum. J Texture Stud 11:351–365

    Article  CAS  Google Scholar 

  95. Vernon-Carter EJ, GÓMez SA, BeristaÍN CI, Mosqueira G, Pedroza-Islas R, Moreno-Terrazas RC (1996) Color degradation and coalescence kinetics aztec of marigold oleoresin-in water emulsions stabilized by mesquite or Arabic gums and their blends. J Texture Stud 27:625–641

    Article  Google Scholar 

  96. Vernon-Carter EJ, Pedroza-Islas R, Beristain CI (1998) Sability of Capsicum annuum Oleoresin-inwater emulsions containing Prosopis and Acacia gums. J Texture Stud 29:553–567

    Article  Google Scholar 

  97. Beristain CI, Vernon-Carter EJ (1994) Utilization of mesquite (Prosopis julijlora) gum as emulsion stabilizing agent for spray-dried encapsulated orange peel oil. Dry Technol 12:1727–1733

    Article  CAS  Google Scholar 

  98. Beristain CI, García HS, Vernon-Carter EJ (1999) Note. Mesquite gum (Prosopis juliflora) and maltodextrin blends as wall materials for spray-dried encapsulated orange peel oil/Nota. Mezclas de goma de mezquite (Prosopis juliflora) y maltodextrina como material encapsulante de aceite esencial de naranja secado por aspersion. Food Sci Technol Int 5:353–356

    Article  CAS  Google Scholar 

  99. Vernon-Carter EJ, Ponce-Palafox JT, Arredondo-Figueroa JL, Pedroza-Islas R (2001) Development of microcapsules containing water and lipid soluble natural colorants for trout pigmentation. J Aquat Food Prod T 10:59–74

    Article  CAS  Google Scholar 

  100. Khanna M, Dwivedi A, Singh S, Soni PL (1997) Mesquite gum (Prosopis juliflora): potential binder in tablet dosage forms. J Sci Ind Res 56:366–368

    CAS  Google Scholar 

  101. Reis AV, Cavalcanti OA, Rubira AF, Muniz EC (2003) Synthesis and characterization of hydrogels formed from a glycidyl methacrylate derivative of galactomannan. Int J Pharm 267:13–25

    Article  CAS  PubMed  Google Scholar 

  102. Barreto S, Maia MS, Benica AM, de Assis H, Leite-Silva VR, da Rocha PA, de Negreiros MMF, Rocha HAD, Ostrosky EA, Lopes PS, Sales VSD, Giordani RB, Ferrari M (2017) Evaluation of in vitro and in vivo safety of the by-product of Agave sisalana as a new cosmetic raw material: development and clinical evaluation of a nanoemulsion to improve skin moisturizing. Ind Crop Prod 108:470–479

    Article  CAS  Google Scholar 

  103. Ribeiro RCD, Barreto S, Ostrosky EA, da Rocha PA, Verissimo LM, Ferrari M (2015) Production and characterization of cosmetic nanoemulsions containing Opuntia ficus-indica (L.) mill extract as moisturizing agent. Molecules 20:2492–2509

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  104. Sirmah P, Mburu F, Iaych K, Dumarçay S, Gérardin P (2011) Potential antioxidant compounds from different parts of prosopis juliflora. J Trop For Sci 23:187–195

    Google Scholar 

  105. Wang S-Y, Wu J-H, Cheng S-S, Lo C-P, Chang H-N, Shyur L-F, Chang S-T (2004) Antioxidant activity of extracts from Calocedrus formosana leaf, bark, and heartwood. J Wood Sci 50:422–426

    Article  CAS  Google Scholar 

  106. Batista R, Santana CC, Azevedo-Santos AV, Suarez-Fontes AM, Ferraz J, Silva LAM, Vannier-Santos MA (2018) In vivo antimalarial extracts and constituents of Prosopis juliflora (Fabaceae). J Funct Food 44:74–78

    Article  CAS  Google Scholar 

  107. Hasan MMU, Azhar I, Muzammil S, Ahmed S, Ahmed SW (2012) Anti-emetic activity of some leguminous plants. Pak J Bot 44:389–391

    Google Scholar 

  108. Choudhary MI, Nawaz SA, Zaheer ul H, Azim MK, Ghayur MN, Lodhi MA, Jalil S, Khalid A, Ahmed A, Rode BM, Atta ur R, Gilani A-u-H, Ahmad VU (2005) Juliflorine: a potent natural peripheral anionic-site-binding inhibitor of acetylcholinesterase with calcium-channel blocking potential, a leading candidate for Alzheimer’s disease therapy. Biochem Biophys Res Commun 332:1171–1179

    Article  CAS  PubMed  Google Scholar 

  109. Patočka J (2008) Juliflorin – naděje na nový lék Alzheimerovy nemoci. Psychiatrie 12:220–222

    Google Scholar 

  110. Malik SK, Ahmed M, Khan F (2018) Identification of novel anticancer terpenoids from Prosopis juliflora (Sw) DC (Leguminosae) pods. Trop J Pharm Res 17:661–668

    Article  Google Scholar 

  111. Souto AL, de Oliveira VM, da Silva VC, Correia MV, da Silva WP, Trindade MAG, Rodrigues CM (2016) Analytical strategies using chromatographic methodologies to analyze lignocellulosic feedstocks and their value-added compounds in biorefinery processes. Springer International Publishing, Cham

    Book  Google Scholar 

  112. Naseeruddin S, Desa S, Linga V (2016) Ethanol production from lignocellulosic substrate Prosopis juliflora. Renew Energ 103:701–707

    Article  CAS  Google Scholar 

  113. Althuri A, Gujjala LKS, Banerjee R (2017) Partially consolidated bioprocessing of mixed lignocellulosic feedstocks for ethanol production. Bioresour Technol 245:530–539

    Article  CAS  PubMed  Google Scholar 

  114. Karthikeyan DS, Prathima A (2016) Emission analysis of the effect of doped nano-additives on biofuel in a diesel engine. Energ Source Part A 38:3702–3708

    Article  CAS  Google Scholar 

  115. Kailappan R, Gothandapani L, Viswanathan R (2000) Production of activated carbon from prosopis (Prosopis juliflora). Bioresour Technol 75:241–243

    Article  CAS  Google Scholar 

  116. Diaz A, Rincon N, Escorihuela A, Fernandez N, Chacin E, Forster CF (1999) A preliminary evaluation of turbidity removal by natural coagulants indigenous to Venezuela. Process Biochem 35:391–395

    Article  CAS  Google Scholar 

  117. Sharmila D, Rebecca J, Saduzzaman M (2013) Biodegradation of tannery effluent using Prosopis juliflora. Int J ChemTech Res 5:2186–2192

    CAS  Google Scholar 

  118. Sharmila D, Rebecca J, Saduzzaman M (2013) Effect of plant extracts on the treatment of paint industry effluent. Int J Pharma Bio Sci 4:B678–B686

    Google Scholar 

  119. Palanisamy SP, Maheswaran G, Kamal C, Ganesan V (2016) Prosopis juliflora—a green corrosion inhibitor for reinforced steel in concrete. Res Chem Intermed 42:7823–7840

    Article  CAS  Google Scholar 

  120. Saini DP, Khan S, Baunthiyal M, Sharma V (2012) Organ-wise accumulation of fluoride in Prosopis juliflora and its potential for phytoremediation of fluoride contaminated soil. Chemosphere 89:633–635

    Article  CAS  PubMed  Google Scholar 

  121. Nivethitha P, Thangavel P, Prince S, Subburam W, Subburam V (2002) Identification of heavy metal cumulating plants and their use in reclamation of soil contaminated with heavy metals. Ecol Environ Conserv 8:249–251

    CAS  Google Scholar 

  122. Senthilkumar P, Prince SW, Sivakumar S, Subbhuraam CV (2005) Prosopis juliflora – a green solution to decontaminate heavy metal (Cu and Cd) contaminated soils. Chemosphere 60:1493–1496

    Article  CAS  PubMed  Google Scholar 

  123. Beramendi-Orosco LE, Rodriguez-Estrada ML, Morton-Bermea O, Romero FM, Gonzalez-Hernandez G, Hernandez-Alvarez E (2013) Correlations between metals in tree-rings of Prosopis julifora as indicators of sources of heavy metal contamination. Appl Geochem 39:78–84

    Article  CAS  Google Scholar 

Download references

Acknowledgments

G.A.B..D., A.L.S., and I.B.S. are recipient of fellowships from the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brazil. The authors wish to thank Ministerio de Ciência, Tecnologia, Inovação e Comunicações – MCTIC and the INCT BioNat for the financial support. M.F. is CNPq fellowship honored researcher.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Raquel Brandt Giordani .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2018 Springer Nature Switzerland AG

About this entry

Check for updates. Verify currency and authenticity via CrossMark

Cite this entry

de Brito Damasceno, G.A., Souto, A.L., da Silva, I.B., Roque, A.d., Ferrari, M., Giordani, R.B. (2018). Prosopis juliflora: Phytochemical, Toxicological, and Allelochemicals. In: Merillon, JM., Ramawat, K. (eds) Co-Evolution of Secondary Metabolites. Reference Series in Phytochemistry. Springer, Cham. https://doi.org/10.1007/978-3-319-76887-8_15-1

Download citation

  • DOI: https://doi.org/10.1007/978-3-319-76887-8_15-1

  • Received:

  • Accepted:

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-76887-8

  • Online ISBN: 978-3-319-76887-8

  • eBook Packages: Springer Reference Chemistry and Mat. ScienceReference Module Physical and Materials ScienceReference Module Chemistry, Materials and Physics

Publish with us

Policies and ethics