References
- Ago H., Kataoka J., Tsuge H., Habuka N., Inagaki E., Noma M., Miyano M., 1994. X-ray Structure of a Pokeweed Antiviral Protein, Coded by a New Genomic Clone, at 0.23 nm Resolution: A Model Structure Provides a Suitable Electrostatic Field for Substrate Binding. European Journal of Biochemistry, 225(1): 369-374, DOI: 10.1111/j.1432-1033.1994.00369.x
- Arabas I., Księżopolski R., 2022. Historia leków naturalnych – nowa odsłona. Kwartalnik nauki i techniki, 67(4): 211-220.
- Baars E.W., Belt-Van Zoen E., Willcox M., Huber R., Hu X.- Y., van der Werf E.T., 2020. CAM treatments for cough and sore throat as part of an uncomplicated acute respiratory tract infection: a systematic review of prescription rates and a survey among European integrative medical practitioners. European Journal of Integrative Medicine, 39, 101194, https://doi.org/10.1016/j.eujim.2020.101194.
- Bajpai V.K., Baek K.-H., Kim E.S., Han J.E., Kwak M., Oh K., Kim J.-C., Kim S., Choi G.J., 2012. In vivo antifungal activities of the methanol extracts of invasive plant species against plant pathogenic fungi. Plant Pathology Journal, 28(3): 317-321, doi: 10.5423/PPJ.NT.04.2012.0056.
- Balogh L., Juhasz M., 2008. American and Chinese pokeweed (Phytolacca americana L., Ph. esculenta van Houtte). pp. 35-46. In: The most invasive plants in Hungary, red.: Botta-Dukat Z., Balogh L.; Institute of ecology and Botany, Hungarian Academy of Sciences, Vacratot, Hungary.
- Barbieri L., Aron G.M., Irvin J.D., Stirpe F., 1982. Purification and partial characterization of another form of the antiviral protein from the seeds of Phytolacca americana L. (poke-weed). The Biochemical journal, 203(1): 55-59, doi: 10.1042/bj2030055.
- Barbieri L., Bolognesi A., Cenini P., Falasca A.I., Minghetti A., Garofano L., Guicciardi A., Lappi D., Miller S.P., Stirpe F., 1989. Ribosome-inactivating proteins from plant cells in culture. The Biochemical journal, 257(3): 801-807, doi: 10.1042/bj2570801
- Barbieri L., Ferreras J.M., Barraco A., Ricci P., Stirpe F., 1992. Some ribosome-inactivating proteins depurinate ribosomal RNA at multiple sites. Biochemical Journal, 286(1): 1-4, doi: 10.1042/bj2860001
- Barbieri L., Lorenzoni E., Stirpe F., 1979. Inhibition of protein-synthesis in vitro by a lectin from momordica-charantia and by other hemagglutinins. Biochemical Journal,182(2): 633-635, doi: 10.1042/bj1820633.
- Barnett B.D., 1975. Toxicity of pokeberries (fruit of Phytolacca americana large) for turkey poults. Poultry science, 54(4): 1215-1217, DOI: 10.3382/ps.0541215
- Baskett C.A., Schroeder L., Weber M.G., Schemske D.W., 2020. Multiple metrics of latitudinal patterns in insect pollination and herbivory for a tropical-temperate congener pair. Ecological Monographs, 90(1), art. no. e01397, doi: 10.1002/ecm.1397.
- Baskett C.A., Schemske D.W., 2018. Latitudinal patterns of herbivore pressure in a temperate herb support the biotic interactions hypothesis. Ecology Letters, 21(4): 578-587.
- Bekeredjian-Ding I., Foermer S., Kirschning C.J., Parcina M., Heeg K., 2012. Poke weed mitogen requires toll-like receptor ligands for proliferative activity in human and murine b lymphocytes. PLoS ONE, 7(1), art. no. e29806, doi: 10.1371/journal.pone.0029806
- Bellavite P., Ortolani R., Pontarollo F., Piasere V., Benato G., Conforti A., 2006. Immunology and homeopathy. 4. Clinical studies - Part 1. Evidence-based Complementary and Alternative Medicine, 3(3): 293-301, doi: 10.1093/ecam/nel045.
- Bentley K.E., Berryman K.R., Hopper M., Hoffberg S.L., Myhre K.E., Iwao K., Lee J.B., Glenn T.C., Mauricio R., 2015. Eleven Microsatellites in an emerging invader, Phytolacca americana (PHYTOLACCACEAE), from its native and introduced ranges. Applications in Plant Sciences, 3(3), art. no. 1500002, doi: 10.3732/apps.1500002.
- Burke D.E., Le Quesne P.W., 1971. 3-acetyloleanolic acid from Phytolacca americana seeds. Phytochemistry, 10(12): 3319-3320, doi: 10.1016/S0031-9422(00)97416-8.
- Cahill Jr. J.F., Casper B.B., 1999. Growth consequences of soil nutrient heterogeneity for two old-field herbs, Ambrosia artemisiifolia and Phytolacca americana, grown individually and in combination. Annals of Botany, 83(4): 471-478, doi: 10.1006/anbo.1999.0841.
- Castagnaro M., Marin M., Ghittino C., Hedrick R.P., 1991. Lectin histochemistry and ultrastructure of rainbow-trout Oncorhynchus mykiss kidneys affected by proliferative kidney-disease. Diseases of Aquatic Organisms, 10(3): 173-183.
- Chaddock J.A., Lord J.M., Hartley M.R., Roberts L.M., 1994. Pokeweed antiviral protein (PAP) mutations which permit E. coli growth do not eliminate catalytic activity towards prokaryotic ribosomes. Nucleic Acids Research, 22(9): 1536-1540, doi: 10.1093/nar/22.9.1536.
- Chen P.D., Hou Y.P., Zhyge Y.-H., Wei W., Huang Q.Q., 2019. The effects of soils from different forest types on the growth of the invasive plant Phytolacca americana. Forests, 10(6), art. no. 492, doi: 10.3390/f10060492
- Chen Y., Zhi J., Zhang H., Li J., Zhao Q., Xu J., 2017. Transcriptome analysis of Phytolacca americana L. in response to cadmium stress. PLoS ONE, 12(9), art. no. e0184681, DOI: 10.1371/journal.pone.0184681
- Chmura D., 2016. Is Phytolacca americana (Phytolaccaceae) a new antropophyte in Polish flora? Fragmenta Floristica et Geobotanica Polonica, 23(1): 172-174.
- Clark A.T.R., Guimarães da Costa V.M.L., Bandeira Costa L., Bezerra Cavalcanti C.L., de Melo Rêgo M.J.B., Beltrão E.I.C., 2014. Differential expression patterns of N-acetylglucosaminyl transferases and polylactosamines in uterine lesions. European Journal of Histochemistry, 58(2), art. no. 2334, 152-157, doi: 10.4081/ejh.2014.2334.
- Day P.J., Lord J.M., Roberts L.M., 1998. The deoxyribonuclease activity attributed to ribosome-inactivating proteins is due to contamination. European Journal of Biochemistry, 258(2): 540-545.
- D’Cruz O.J., Uckun F.M., 2001a. Effect of pretreatment of semen with pokeweed antiviral protein on pregnancy outcome in the rabbit model. Fertility and Sterility, 76(4): 830-833, doi: 10.1016/S0015-0282(01)01992-6.
- D’Cruz O.J., Uckun F.M., 2001b. Pokeweed antiviral protein: A potential nonspermicidal prophylactic antiviral agent. Fertility and Sterility, 75(1): 106-114, doi: 10.1016/S0015-0282(00)01665-4.
- D’Cruz O.J., Waurzyniak B., Uckun F.M., 2004. Mucosal Toxicity Studies of a Gel Formulation of Native Pokeweed Antiviral Protein. Toxicologic Pathology, 32(2): 212-221, doi: 10.1080/01926230490274362.
- de Groot M., Kozamernik E., Kermavnar J., Kolšek M., Marinšek A., Nève Repe A., Kutnar L., 2024. Importance of Habitat Context in Modelling Risk Maps for Two Established Invasive Alien Plant Species: The Case of Ailanthus altissima and Phytolacca americana in Slovenia (Europe). Plants, 13(6): art. no. 883, doi: 10.3390/plants13060883.
- de Groot M., O’hanlon R., Bullas-Appleton E., Csóka G., Csiszár Á., Faccoli M., Gervasini E., Kirichenko N., Korda M., Marinšek A., Robinson N., Shuttleworth C., Sweeney J., Tricarico E., Verbrugge L., Williams D., Zidar S., Veenvliet J.K., 2020. Challenges and solutions in early detection, rapid response and communication about potential invasive alien species in forests. Management of Biological Invasions, 11(4): 637-660, doi: 10.3391/mbi.2020.11.4.02.
- Demirkan E., Ertürk E., Yildiz G., Sevgi T., Çetinkaya A.A., 2022. In vitro evaluations of antioxidant, antimicrobial and anticancer potential of Phytolacca americana L. (pokeweed) seed extract. Trakya University Journal of Natural Sciences, 23(2): 135-143.
- Di R., 2016. Complete genome sequence of the pokeweed mosaic virus (PkMV)-New Jersey isolate and its comparison to PkMV-MD and PkMV-PA. Genome Announcements, 4(5), art. no. e00929-16, doi: 10.1128/genomeA.00929-16.
- Diepenbrock L.M., Swoboda-Bhattarai K.A., Burrack H.J., 2016. Ovipositional preference, fidelity, and fitness of Drosophila suzukii in a co-occurring crop and non-crop host system. Journal of Pest Science, 89(3): 761-769, doi: 10.1007/s10340-016-0764-5.
- Dogan Y., Nedelcheva A., Łukasz Łuczaj, Drăgulescu C., Stefkov G., Maglajlić A., Ferrier J., Papp N., Hajdari A., Mustafa B., Dajić-Stevanović Z., Pieroni A., 2015. Of the importance of a leaf: the ethnobotany of sarma in Turkey and the Balkans. Journal of Ethnobiology and Ethnomedicine, 11, Article number: 26.
- Do Kim B., Chun Kim H., Tae Yoo S., Geun Choi Y., Koo Kang S., Won Yoon J., Song Kim G., 2013. Flora of Vascular Plants in Ridgelines in the Palgongsa Procincial Park, Korea. Journal of Asia-Pacific Biodiversity, 6(2): 311-328, doi: 10.7229/jkn.2013.6.2.311.
- Domaradzki K., Dobrzański A., Jezierska-Domaradzka A., 2013. Invasive plants – occurrence, importance and threat to biodiversity. Progress in Plant Protection/Postępy w Ochronie Roślin, 53(3): 613-620. (in Polish + summary in English)
- Domashevskiy A.V., Miyoshi H., Goss D.J., 2012. Inhibition of Pokeweed Antiviral Protein (PAP) by turnip mosaic virus genome-linked protein (VPg). Journal of Biological Chemistry, 287(35): 29729-29738, doi: 10.1074/jbc.M112.367581
- Dong W., Hyde K.D., Jeewon R., Liao C.F., Zhao H.J., Kularathnage N.D., Li H., Yang Y.H., Pem D., Shu Y.X., Gafforov Y., Manawasinghe I.S., Doilom M., 2023. Mycosphere notes 449–468: saprobic and endophytic fungi in China, Thailand, and Uzbekistan. Mycosphere, 14(1): 2208-2262, doi: 10.5943/mycosphere/14/1/26.
- Dore J.-M., Gras E., Depierre F., Wijdenes J., 1993. Mutations dissociating the inhibitory activity of the pokeweed antiviral portein on eukaryote translation and Escherichia coli growth. Nucleic Acids Research, 21(18): 4200-4205, doi: 10.1093/nar/21.18.4200.
- Dou C., Qi C., 2023. Rhizospheric Precipitation of Manganese by Phosphate: A Novel Strategy to Enhance Mn Tolerance in the Hyperaccumulator Phytolacca americana. Toxics, 11(12), art. no. 977, doi: 10.3390/toxics11120977.
- Dougherty K., Prashar T., Hudak K.A., 2024. Improved poke-weed genome assembly and early gene expression changes in response to jasmonic acid. BMC Plant Biology, 24(1), art. no. 801, doi: 10.1186/s12870-024-05446-1.
- Essert S., Koštro A., Hruševar D., 2023. Vascular flora of Tuškanac Forest Park (Zagreb, Croatia). Natura Croatica, 32(1): 159-175, doi: 10.20302/NC.2023.32.11
- Faragó A., Zvara Á., Tiszlavicz L., Hunyadi-Gulyás É., Darula Z., Hegedűs Z., Szabó E., Surguta S.E., Tóvári J., Puskás L.G., Szebeni G.J., 2024. Lectin-Based Immunophenotyping and Whole Proteomic Profiling of CT-26 Colon Carcinoma Murine Model. International Journal of Molecular Sciences, 25(7), art. no. 4022, doi: 10.3390/ijms25074022.
- Fenner R., Betti A.H., Mentz L.A., Rates S.M.K., 2006. Plants with potencial antifungal activity employed in Brazilian folk medicine. Revista Brasileira de Ciencias Farmaceuticas/Brazilian Journal of Pharmaceutical Sciences, 42(3): 369-394, doi: 10.1590/S1516-93322006000300007.
- Follak S., Schwarz M., Essl F., 2022. Notes on the occurrence of Phytolacca americana L. in crop fields and its potential agricultural impact. BioInvasions Records, 11(3): 620-630, doi: 10.3391/bir.2022.11.3.04.
- Fujitaka Y., Hamada H., Hamada H., Iwaki T., Shimoda K., Kiriake Y., Saikawa T., 2020. Synthesis of Glycosides of α-Tocopherol, Daidzein, Resveratrol, Hesperetin, Naringenin, and Chrysin as Antiallergic Functional Foods and Cosmetics. Natural Product Communications, 15(9), doi: 10.1177/1934578X20944666.
- Fujitaka Y., Shimoda K., Araki M., Doi S., Ono T., Hamada H., Hamada H., 2017. Biotransformation of daidzein to diadzein-7-glucoside and its anti-allergic activity. Natural Product Communications, 12(11): 1741-1742.
- Fujitaka Y., Shimoda K., Kubota N., Araki M., Onishi T., Nakayama N., Ishihara K., Tanigawa M., Hamada H., Hamada H., 2017. Glycosylation and methylation of quercetin and myricetin by cultured cells of Phytolacca americana. Natural Product Communications, 12(4): 523-524, doi: 10.1177/1934578x1701200415 https://www.scopus.com/inward/record.uri?eid=2-s2.0-.
- Gandhi R., Manzoor M., Hudak K.A., 2008. Depurination of brome mosaic virus RNA3 in vivo results in translation-dependent accelerated degradation of the viral RNA. Journal of Biological Chemistry, 283(47): 32218-32228, doi: 10.1074/jbc.M803785200.
- George Thompson A.M., Iancu C.V., Nguyen T.T.H., Kim D., Choe J.-Y., 2015. Inhibition of human GLUT1 and GLUT5 by plant carbohydrate products insights into transport specificity. Scientific Reports, 5, art. no. 12804.
- Gras A., Garnatje T., Ibáñez N., López-Pujol J., Nualart N., Vallès J., 2017. Medicinal plant uses and names from the her-barium of Francesc Bolòs (1773–1844). Journal of Ethnopharmacology, 204: 142-168, doi: 10.1016/j.jep.2017.04.002.
- Grosjean N., Le Jean M., Berthelot Ch., Chalot M.L., Gross E.M., Blaudez D., 2019. Accumulation and fractionation of rare earth elements are conserved traits in the Phytolacca genus. Scientific Report, 9: 18458.
- Guo Y., Chen K., Lei S., Gao Y., Yan S., Yuan M., 2023. Rare Earth Elements (REEs) Adsorption and Detoxification Mechanisms in Cell Wall Polysaccharides of Phytolacca americana L. Plants, 12(10), art. no. 1981, doi: 10.3390/plants12101981
- Guzzetti L., Galimberti A., Bruni I., Magoni C., Ferri M., Tassoni A., Sangiovanni E., Dell’Agli M., Labra M., 2017. Bioprospecting on invasive plant species to prevent seed dispersal. Scientific Reports, 7(1): art. no. 13799, doi: 10.1038/s41598-017-14183-5.
- Habermann H.M., 1960. Light-dependent oxygen metabolism of chloroplast preparations. 2. Stimulation by manganous ions. Plant Physiology, 35(3): 307-312.
- Hamada H., Hamada H., Ishihara K., Kuboki A., Iwaki T., Kiriake Y., 2021. Enzymatic synthesis of α-tocopherol derivative glycoside, daidzein glycoside, daidzein oligosaccharide, resveratrol oligosaccharide, and curcumin oligosaccharides and their anti-allergic activity and neuroprotective activity. Natural Product Communications, 16(10), doi: 10.1177/1934578X211029095.
- Hamada H., Hamada H., Shimoda K., 2015. Synthesis of ε-viniferin glycosides by glucosyltransferase from Phytolacca americana and their inhibitory activity on histamine release from rat peritoneal mast cells. Natural Product Communications, 10(6), doi: 10.1177/1934578X1501000655.
- Hamada H., Ohiwa S., Nishida T., Katsuragi H., Takeda T., Hamada H., Nakajima N., Ishihara K., 2003. One-step Glucosylation of Capsaicinoids by Cultured Cells of Phytolacca americana. Plant Biotechnology, 20(3): 253-255, doi: 10.5511/plantbiotechnology.20.253.
- Hamada H., Okada S., Shimoda K., Uesugi D., Hamada H., 2016. Optical resolution of (RS)-denopamine to (R)-denopamine β-DGlucoside by glucosyltransferase from Phytolacca americana expressed in recombinant Escherichia coli. Natural Product Communications, 11(8): 1121-1122, doi: 10.1177/1934578x1601100823.
- Hamada H., Shimoda K., Horio Y., Ono T., Hosoda R., Nakayama N., Urano K., 2017. Pterostilbene and its glucoside induce type XVII collagen expression. Natural Product Communications, 12(1): 85-86, doi: 10.1177/1934578x1701200123.
- Han H.-Y., Han K.-H., Ahn J.-H., Park S.-M., Kim S., Lee B.-S., Min B.-S., Yoon S., Oh J.-H., Kim T.-W., 2020. Subchronic Toxicity Assessment of Phytolacca americana L. (Phytolaccaceae) in F344 Rats. Natural Product Communications, 15(7), doi: 10.1177/1934578X20941656.
- Hartley M.R., Legname G., Osborn R., Chen Z., Lord J.M., 1991. Single-chain ribosome inactivating proteins from plants depurinate Escherichia coli 23S ribosomal RNA. FEBS Letters, 290(1-2): 65-68, doi: 10.1016/0014-5793(91)81227-Y.
- Hassan Y., Ogg S., Ge H., 2018. Expression of novel fusion anti-viral proteins ricin a chain-pokeweed antiviral proteins (RTAPAPs) in Escherichia coli and their inhibition of protein synthesis and of hepatitis B virus in vitro. BMC Biotechnology, 18(1), art. no. 47, doi: 10.1186/s12896-018-0458-6.
- Hassan Y., Ogg S., Ge H., 2020. Novel binding mechanisms of fusion broad range anti-infective protein ricin a chain mutant-pokeweed antiviral protein 1 (RTAM-PAP1) against SARSCoV-2 key proteins in silico. Toxins, 12(9), art. no. 602, doi: 10.3390/toxins12090602.
- He J.-S., Bazzaz F.A., 2003. Density-dependent responses of reproductive allocation to atmospheric CO2 in Phytolacca americana. New Phytologist, 157(2): 229-239, doi: 10.1046/j.1469-8137.2003.00660.x.
- He J.-S., Flynn D.F.B., Wolfe-Bellin K., Fang J., Bazzaz F.A., 2005. CO2 and nitrogen, but not population density, alter the size and C/N ratio of Phytolacca americana seeds. Functional Ecology, 19(3): 437-444, doi: 10.1111/j.1365-2435.2005.00981.x.
- Hirano H., Sakuta M., Komamine A., 1992. Inhibition by cytokinin of the accumulation of betacyanin in suspension cultures of Phytolacca americana. Zeitschrift fur Naturforschung - Section C Journal of Biosciences, 47(9-10): 705-710, doi: 10.1515/znc-1992-9-1012.
- Hirano H., Sakuta M., Komamine A., 1996. Inhibition of beta-cyanin accumulation by abscisic acid in suspension cultures of Phytolacca americana. Zeitschrift fur Naturforschung Section C - Journal of Biosciences, 51(11-12): 818-822, doi: 10.1515/znc-1996-11-1209.
- Hiyama T., Yumoto K., Satoh A., Takahashi M., Nishikido T., Nakamoto H., Suzuki K., Hiraide T., 2000. Chromatographic separation of a small subunit (PsbW/PsaY) and its assignment to Photosystem I reaction center. Biochimica et Biophysica Acta - Bioenergetics, 1459(1): 117-124, doi: 10.1016/S0005-2728(00)00120-1.
- Homann P.H., 1988. Structural effects of Cl- and other anions on the water oxidizing complex of chloroplast photosystem-II. Plant Physiology, 88(1): 194-199.
- Homma T., Hirai K., Kwon S., Katsuragi H., Hamada H., Katayama Y., 2008. Actions of capsaicin glucosides on intestinal transport in rats. Electrochemistry, 76(8): 583-585, doi: 10.5796/electrochemistry.76.583.
- Honjo E., Watanabe K., 1999. Expression of mature pokeweed antiviral protein with or without C-terminal extrapeptide in Escherichia coli as a fusion with maltose-binding protein. Bioscience Biotechnology and Biochemistry, 63(7): 1291-1294.
- Hu H., Yang Y., Aissa A., Tekin V., Li J., Panda S.K., Huang H., Luyten W., 2022. Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments. BMC Complementary Medicine and Therapies, 22(1), art. no. 244, doi: 10.1186/s12906-022-03712-z.
- Hudak K.A., Bauman J.D., Tumer N.E., 2002. Pokeweed anti-viral protein binds to the cap structure of eukaryotic mRNA and depurinates the mRNA downstream of the cap. RNA, 8(9): 1148-1159, doi: 10.1017/S1355838202026638.
- Hur Y., Hwang D.-J., Zoubenko O., Coetzer C., Uckun F.M., Tumer N.E., 1995. Isolation and characterization of poke-weed antiviral protein mutations in Saccharomyces cerevisiae: Identification of residues important for toxicity. Proceedings of the National Academy of Sciences of the United States of America, 92(18): 8448-8452, doi: 10.1073/pnas.92.18.8448.
- Iglesias A., Cancela Á., Soler Baena A., Sánchez Á., 2023. Characterization of Cellulose Derived from Invasive Alien Species Plant Waste for Application in the Papermaking Industry: Physic-Mechanical, Optical, and Chemical Property Analysis. Applied Sciences (Switzerland), 13(20), art. no. 11568, doi: 10.3390/app132011568.
- Iida T., Mitamura T., Kobayashi H., Suzuki K., 1983. Photoelectrochemical hydrogen production by a photocell using the Phytolacca americana photosystem I particles-methylviologen system. Agricultural and Biological Chemistry, 47(1): 175-177, doi: 10.1271/bbb1961.47.175.
- Irvin J.D., Aron G.M., 1982. Chemical modifications of Poke-weed antiviral protein: effects upon ribosome inactivation, antiviral activity and cytotoxicity. FEBS Letters, 148(1): 127-130, doi: 10.1016/0014-5793(82)81257-X.
- Islam M.R., Kung S.-S., Kimura Y., Funatsu G., 1991. NAcetyl-D-glucosamine-Asparagine Structure in Ribosomeinactivating Proteins from the Seeds of Luffa cylindrica and Phytolacca americana. Agricultural and Biological Chemistry, 55(5): 1375-1381, doi: 10.1271/bbb1961.55.1375.
- Itakura Y., Nakamura-Tsuruta S., Kominami J., Tateno H., Hirabayashi J., 2017. Sugar-binding profiles of chitin-binding lectins from the hevein family: A comprehensive study. International Journal of Molecular Sciences, 18(6), art. no. 1160, doi: 10.3390/ijms18061160.
- Iwakiri T., Imai H., Hamada H., Nakayama T., Ozaki S.-I., 2013. Synthesis of 3,5,3′,4′-tetrahydroxy-trans-stilbene-4′-O-β-dglucopyranoside by glucosyltransferases from Phytolacca americana. Natural Product Communications, 8(1): 119-120, doi: 10.1177/1934578x1300800128.
- Iwakiri T., Mase S., Murakami T., Matsumoto M., Hamada H., Nakayama T., Ozaki S., 2013. Glucosylation of hydroxyflavones by glucosyltransferases from Phytolacca americana. Journal of Molecular Catalysis B-Enzymatic, 90: 61-65.
- Jajor E., Mrówczyński M. (red.), 2016. Metodyka integrowanej ochrony i produkcji rzepaku ozimego oraz jarego dla doradców. IOR-PIB Poznań.
- Jasińska J.M., Michalska K, Szuwarzyński M., Mazur T., Cholewa-Wójcik A., Kopeć M., Juszczak L., Kamińska I., Nowak N., Jamróz E., 2024. Phytolacca americana extract as a quality-enhancing factor for biodegradable double-layered films based on furcellaran and gelatin - Property assessment. International Journal of Biological Macromolecules, 279, 135155.
- Jones C.J.P., Carter A.M., Bennett N.C., Blankenship T.N., Enders A.C., 2009. Placentation in the Hottentot Golden Mole, Amblysomus hottentotus (Afrosoricida: Chrysochloridae). Placenta, 30(7): 571-578, doi: 10.1016/j.placenta.2009.04.014.
- Jones C.J.P., Silvia W.J., Hamilton C.H., Geary T.W., Zezeski A.L., Wooding F.B.P., 2017. Glycosylation and immunocytochemistry of binucleate cells in pronghorn (Antilocapra americana, Antilocapridae) show features of both Giraffidae and Bovidae. Placenta, 57: 216-222, doi: 10.1016/j.placenta.2017.07.011.
- Joy R.W., Sugiyama M., Fukuda H., Komamine A., 1995. Cloning and characterization of polyphenol oxidase cDNAs of Phytolacca-americana. Plant Physiology, 107(4): 1083-1089.
- Kanzaki H., Kagemori T., Yamachika Y., Nitoda T., Kawazu K., 1999. Inhibition of plant transformation by phytolaccoside b from Phytolacca americana callus. Bioscience, Biotechnology and Biochemistry, 63(9): 1657-1659, doi: 10.1271/bbb.63.1657.
- Karami M., Naghshvar F., Saeidnia S., Omrani N., 2010. Hepatoxicity of aqueous extract and fractionated methanol extract of Phytolacca americana by isolated rat liver perfusion system. African Journal of Biotechnology, 9(8): 1211-1217, doi: 10.5897/ajb2010.000-3013.
- Kataoka J., Ago H., Habuka N., Furuno M., Masuta C., Miyano M., Koiwai A., 1993. Expression of a pokeweed antiviral protein in Escherichia coli and its characterization. FEBS Letters, 320(1): 31-34, doi: 10.1016/0014-5793(93)81651-F.
- Kenis M., Tonina L., Eschen R., van der Sluis B., Sancassani M., Mori N., Haye T., Helsen H., 2016. Non-crop plants used as hosts by Drosophila suzukii in Europe. Journal of Pest Science, 89(3): 735-748, doi: 10.1007/s10340-016-0755-6.
- Kim H.-R., You Y.-H., 2010. Effects of elevated CO2 concentration and increased temperature on leaf related-physiological responses of Phytolacca insularis (native species) and Phytolacca americana (invasive species). Journal of Ecology and Field Biology, 33(3): 195-204, doi: 10.5141/JEFB.2010.33.3.195.
- Kobayashi A., Hagihara K., Kajiyama S.-I., Kanzaki H., Kawazu K., 1995. Antifungal compounds induced in the dual culture with Phytolacca americana callus and Botrytis fabae. Zeitschrift fur Naturforschung - Section C Journal of Biosciences, 50(5-6): 398-402, DOI: 10.1515/znc-1995-5-610
- Kopij G., 2023. The first record of the pokeweed Phytolacca americana (Phytolaccaceae) in southwestern Poland. Fragmenta Floristica Geobotanica Polonica, 28(1): 88-91.
- Kung S.-S., Kimura M., Funatsu G., 1990. The complete amino acid sequence of antiviral protein from the seeds of pokeweed (Phytolacca americana). Agricultural and Biological Chemistry, 54(12): 3301-3318, doi: 10.1271/bbb1961.54.3301.
- Kwak M., Troiano E., Kil E.-J., Parrella G., 2024. High-throughput sequencing detected a virus-viroid complex in a single pokeweed plant. Frontiers in Plant Science, 15: 1435611, doi: 10.3389/fpls.2024.1435611.
- Lee J.C., Dreves A.J., Cave A.M., Kawai S., Isaacs R., Miller J.C., Timmeren S.V., Bruck D.J., 2015. Infestation of wild and ornamental noncrop fruits by Drosophila suzukii (Diptera: Drosophilidae). Annals of the Entomological Society of America, 108(2): 117-129, doi: 10.1093/aesa/sau014.
- Lee S.-H., Kim S., Kim H.-J., 2018. Effects of thinning intensity on understory vegetation in Chamaecyparis obtusa stands in South Korea. Forest Science and Technology, 14(1): 7-15, doi: 10.1080/21580103.2017.1409661.
- Li L., Li Y., Wang X., 2012. Generation of High Titre Antibodies to Pokeweed Antiviral Protein (PAP) in Rabbits Using Synthetic Peptides and their Use in Detecting PAP in Transgenic Petunia and Yeast. Journal of Phytopathology, 160(10): 599-602, doi: 10.1111/j.1439-0434.2012.01942.x.
- Li T., Luo B., Tong Y., Wei G., Chai L., Hu R., 2024. Medicinal flora of the baiku yao people — An ethnobotanical documentation in South China. BMC Complementary Medicine and Therapies, 24(1), art. no. 242, doi: 10.1186/s12906-024-04545-8.
- Liu B., Wang G., An Y., Xue D., Wang L., Lu C., 2021. Similar seed dispersal systems by local frugivorous birds in native and alien plant species in a coastal seawall forest. PeerJ, art. no. e11672, doi: 10.7717/peerj.11672.
- Liu D., Chen L., Chen C., An X., Zhang Y., Wang Y., Li Q., 2020. Full-length transcriptome analysis of Phytolacca americana and its congener P. icosandra and gene expression normalization in three Phytolaccaceae species. BMC Plant Biology, 20(1), art. no. 396, doi: 10.1186/s12870-020-02608-9.
- Liu D., Chen L., Chen C., Zhou Y., Xiao F., Wang Y., Li Q., 2022. Effect of plant VOCs and light intensity on growth and reproduction performance of an invasive and a native Phytolacca species in China. Ecology and Evolution, 12(3), art. no. e8522, doi: 10.1002/ece3.8522.
- Liu D., Liu M., Ju R., Li B., Wang Y., 2024. Rapid seedling emergence of invasive Phytolacca americana is related to higher soluble sugars produced by starch metabolism and photosynthesis compared to native P. acinosa. Frontiers in Plant Science, 15, art. no. 1255698, doi: 10.3389/fpls.2024.1255698.
- Liu Y., Luo J., Xu C., Ren F., Peng C., Wu G., Zhao J., 2000. Purification, characterization, and molecular cloning of the gene of a seed-specific antimicrobial protein from poke-weed. Plant Physiology, 122(4): 1015-1024, doi: 10.1104/pp.122.4.1015.
- Lodge J.K., Kaniewski W.K., Tumer N.E., 1993. Broad-spectrum virus resistance in transgenic plants expressing poke-weed antiviral protein. Proceedings of the National Academy of Sciences of the United States of America, 90(15): 7089-7093, doi: 10.1073/pnas.90.15.7089.
- Lopes A.I.F., Monteiro M., Araújo A.R.L., Rodrigues A.R.O., Castanheira E.M.S., Pereira D.M., Olim P., Fortes A.G., Gonçalves M.S.T., 2020. Cytotoxic Plant Extracts towards Insect Cells: Bioactivity and Nanoencapsulation Studies for Application as Biopesticides. Molecules, 25(24), art. no. 5855, doi: 10.3390/MOLECULES25245855.
- Maharjan R., Fukuda Y., Nakayama T., Nakayama T., Hamada H., Ozaki S.-I., Inoue T., 2022. Structural basis for substrate recognition in the Phytolacca americana glycosyltransferase PaGT3. Acta Crystallographica Section D: Structural Biology, 78: 379-389, doi: 10.1107/S2059798322000869.
- Maharjan R., Fukuda Y., Shimomura N., Nakayama T., Okimoto Y., Kawakami K., Nakayama T., Hamada H., Inoue T., Ozaki S.-I., 2020. An Ambidextrous Polyphenol Glycosyltransferase PaGT2 from Phytolacca americana. Biochemistry, 59(27): 2551-2561, doi: 10.1021/acs.biochem.0c00224.
- Marinas I.C., Gradisteanu Pircalabioru G., Oprea E., Geana E.-I., Zgura I., Romanitan C., Matei E., Angheloiu M., Brincoveanu O., Georgescu M., Chifiriuc M.C., 2023. Physico-chemical and pro-wound healing properties of microporous cellulosic sponge from Gleditsia triacanthos pods functionalized with Phytolacca americana fruit extract. Cellulose, 30(16): 10313-10339, doi: 10.1007/s10570-023-05491-3.
- Marinaş I.C., Oprea E., Geană E.-I., Luntraru C.M., Gîrd C.E., Chifiriuc M.-C., 2021. Chemical composition, antimicrobial and antioxidant activity of Phytolacca americana L. fruits and leaves extracts. Farmacia, 69(5): 883-889, doi: 10.31925/FARMACIA.2021.5.9.
- Matsuda K., Niitsuma A., Uchida M.K., Suzuki-Nishimura T., 1994. Inhibitory Effects of Sialic Acid- or N-Acetylglucosamine-Specific Lectins on Histamine Release Induced by Compound 48/80, Bradykinin and a Polyethylenimine in Rat Peritoneal Mast Cells. Japanese Journal of Pharmacology, 64(1): 1-8, doi: 10.1254/jjp.64.1.
- Mikulic-Petkovsek M., Veberic R., Hudina M., Misic E., 2022. HPLC-DAD-MS Identification and Quantification of Phenolic Components in Japanese Knotweed and American Pokeweed Extracts and Their Phytotoxic Effect on Seed Germination. Plants, 11(22), art. no. 3053, doi: 10.3390/plants11223053.
- Milner M., French C.S., Milner H.W., 1958. Effect of petroleum ether extraction and readdition of various compounds on the photochemical activity of isolated chloroplasts. Plant Physiology, 33(5): 367-372.
- Minami Y., Higuchi S., Yagi F., Tadera K., 1998. Isolation and some properties of the antimicrobial peptide (pa-amp) from the seeds of pokeweed (Phytolacca americana). Bioscience, Biotechnology and Biochemistry, 62(10): 2076-2078, doi: 10.1271/bbb.62.2076.
- Minic Z., Leproust-Lecoester L., Laporte J., De Kouchkovsky Y., Brown S.C., 2000. Proteins isolated from lucerne roots by affinity chromatography with sugars analogous to Nod factor moieties. Biochemical Journal, 345(2): 255-262, doi: 10.1042/0264-6021:3450255.
- Mishra M.D., Hammond R.W., Owens R.A., Smith D.R., Diener T.O., 1991. Indian bunchy top disease of tomato plants is caused by a distinct strain of citrus exocortis viroid. Journal of General Virology, 72: 1781-1785.
- Mosyakin S.L., Mosyakin A.S., 2021. Lockdown botany 2020: some noteworthy records of alien plants in Kyiv City and Kyiv Region. Ukrainian Botanical Journal, 78(2): 96-111, doi: 10.15407/ukrbotj78.02.096.
- Nan Q., Li C., Li X., Zheng D., Li Z., Zhao L., 2024. Modeling the potential distribution patterns of the invasive plant species Phytolacca americana in China in Response to Climate Change. Plants, 13(8), art. no. 1082, doi: 10.3390/plants13081082.
- Neller K.C.M., Diaz C.A., Platts A.E., Hudak K.A., 2019. De novo Assembly of the Pokeweed Genome Provides Insight Into Pokeweed Antiviral Protein (PAP) Gene Expression. Frontiers in Plant Science, 10, art. no. 1002, doi: 10.3389/fpls.2019.01002.
- Neller K.C.M., Klenov A., Guzman J.C., Hudak K.A., 2018. Integration of the pokeweed miRNA and mRNA transcriptomes reveals targeting of jasmonic acid-responsive genes. Frontiers in Plant Science, 9, art. no. 589, doi: 10.3389/fpls.2018.00589.
- Neller K.C.M., Klenov A., Hudak K.A., 2016. The pokeweed leaf mRNA transcriptome and its regulation by jasmonic acid. Frontiers in Plant Science, 7 (MAR2016), art. no. 283, doi: 10.3389/fpls.2016.00283.
- Neller K.C.M., Klenov A., Hudak K.A., 2019. Prediction and Characterization of miRNA/Target Pairs in Non-Model Plants Using RNA-seq. Current protocols in plant biology, 4(2), pp. e20090, doi: 10.1002/cppb.20090.
- Noguchi A., Kunikane S., Homma H., Liu W., Sekiya T., Ho-soya M., Kwon S., Ohiwa S., Katsuragi H., Nishino T., Takahashi S., Hamada H., Nakayama T., 2009. Identification of an inducible glucosyltransferase from Phytolacca americana L. cells that are capable of glucosylating capsaicin. Plant Biotechnology, 26(3): 285-292, doi: 10.5511/plant-biotechnology.26.285.
- Omokawa H., Ichizen N., Konnai M., Takematsu T., 1988. Herbicidal Activity and Phytotoxic Properties of N-Alkyl-N′-(α, α, dimethylbenzyl)-2, 4-diamino-6-chloro-s-triazines. Agricultural and Biological Chemistry, 52(6): 1515-1519, doi: 10.1271/bbb1961.52.1515.
- Orrock J.L., Christopher C.C., 2010. Density of intraspecific competitors determines the occurrence and benefits of accelerated germination. American Journal of Botany, 97(4): 694-699, doi: 10.3732/ajb.0900051.
- Orrock J.L., Levey D.J., Danielson B.J., Damschen E.I., 2006. Seed predation, not seed dispersal, explains the landscape-level abundance of an early-successional plant. Journal of Ecology, 94(4): 838-845, doi: 10.1111/j.1365-2745.2006.01125.x.
- Osathanunkul M., Madesis P., 2019. Bar-HRM: A reliable and fast method for species identification of ginseng (Panax ginseng, Panax notoginseng, Talinum paniculatum and Phytolacca Americana). PeerJ, 2019 (9), art. no. e7660, doi: 10.7717/peerj.7660.
- Ozaki S., Imai H., Iwakiri T., Sato T., Shimoda K., Nakayama T., Hamada H., 2012. Regioselective glucosidation of transresveratrol in Escherichia coli expressing glucosyltransferase from Phytolacca americana. Biotechnology Letters, 34(3): 475-481, doi: 10.1007/s10529-011-0784-4.
- Pandey A., Gupta N., Gupta S.C., 2009. Improvement of in vitro oocyte maturation with lectin supplementation and expression analysis of Cx43, GDF-9, FGF-4 and Fibronectin mRNA transcripts in Buffalo (Bubalus bubalis). Journal of Assisted Reproduction and Genetics, 26(6): 365-371, doi: 10.1007/s10815-009-9314-x.
- Panero I., Fiorentino F., La Montagna D., Crocenzi G., Attorre F., Fabrini G., 2024. Germination ecology of Phytolacca americana L. in its invasive range. Plant Species Biology, doi: 10.1111/1442-1984.12483.
- Panno S., Caruso A.G., Bertacca S., Matic S., Davino S., Parrella G., 2021. Detection of Parietaria Mottle Virus by RT-qPCR: An Emerging Virus Native of Mediterranean Area That Undermine Tomato and Pepper Production in Southern Italy. Frontiers in Plant Science, 12, article 698573.
- Parikh B.A., Coetzer C., Tumer N.E., 2002. Pokeweed antiviral protein regulates the stability of its own mRNA by a mechanism that requires depurination but can be separated from depurination of the α-sarcin/ricin loop of rRNA. Journal of Biological Chemistry, 277(44): 41428-41437, doi: 10.1074/jbc.M205463200.
- Park S.-W., Lawrence C.B., Linden J.C., Vivanco J.M., 2002. Isolation and characterization of a novel ribosome-inactivating protein from root cultures of pokeweed and its mechanism of secretion from roots. Plant Physiology, 130(1): 164-178, doi: 10.1104/pp.000794.
- Parrella G., Troiano E., Stinca A., Pozzi M.I., 2021. Molecular and serological detection of Parietaria mottle virus in Phytolacca americana, a new host of the virus. Phytopathologia Mediterranea, 60(1): 101-104, doi: 10.36253/phyto-12207.
- Patra J.K., Kim E.S., Oh K., Kim H.-J., Kim Y., Baek K.-H., 2014. Antibacterial effect of crude extract and metabolites of Phytolacca americana on pathogens responsible for periodontal inflammatory diseases and dental caries. BMC Complementary and Alternative Medicine, 14(1), art. no. 343, doi: 10.1186/1472-6882-14-343.
- Pepe M., Crescente M.F., Varone L., 2022. Effect of water stress on physiological and morphological leaf traits: A comparison among the three widely-spread invasive alien species Ailanthus altissima, Phytolacca americana, and Robinia pseudoacacia. Plants, 11(7), art. no. 899, doi: 10.3390/plants11070899.
- Pepe M., Gratani L., Crescente M.F., Puglielli G., Varone L., 2022. Daily temperature effect on seedling growth dynamic of three invasive alien species. Frontiers in Plant Science, 13, art. no. 837449, doi: 10.3389/fpls.2022.837449.
- Pérez-Campos-Mayoral L., Ruiz-Argüelles A., Pérez-Romano B., Zenteno E., Hernández-Cruz P., Martínez-Cruz R., Martínez-Cruz M., Pina-Canseco S., Pérez-Campos E., 2008. Potential use of the Macrobrachium rosenbergii lectin for diagnosis of T-cell acute lymphoblastic leukemia. Tohoku Journal of Experimental Medicine, 214(1): 11-16, doi: 10.1620/tjem.214.11.
- Phytolacca americana in Poland. https://www.inaturalist.org/places/poland#q=Phytolacca%2Bamericana. (accessed 9.12.2024)
- Picard D., Kao C.C., Hudak K.A., 2005. Pokeweed antiviral protein inhibits brome mosaic virus replication in plant cells. Journal of Biological Chemistry, 280(20): 20069-20075, doi: 10.1074/jbc.M413452200.
- Poyet J.-L., Hoeveler A., 1997. Presence of an intron in a gene of PAP II, the ribosome-inactivating protein from summer leaves of Phytolacca americana. Annals of Botany, 80(5): 685-688, doi: 10.1006/anbo.1997.0478.
- Poyet J.-L., Radom J., Hoeveler A., 1994. Isolation and characterization of a cDNA clone encoding the pokeweed antiviral protein II from Phytolacca americana and its expression in E. coli. FEBS Letters, 347(2-3): 268-272, doi: 10.1016/0014-5793(94)00565-6.
- Prestle J., Schönfelder M., Adam G., Mundry K.-W., 1992. Type 1 ribosome-inactivating proteins depurinate plant 25S rRNA without species specificity. Nucleic Acids Research, 20(12): 3179-3182, doi: 10.1093/nar/20.12.3179.
- Rajamohan F., Pugmire M.J., Kurinov I.V., Uckun F.M., 2000. Modeling and alanine scanning mutagenesis studies of recombinant pokeweed antiviral protein. Journal of Biological Chemistry, 275(5): 3382-3390, doi: 10.1074/jbc.275.5.3382.
- Rajamohan F., Mao C., Uckun F.M., 2001. Binding interactions between the active center cleft of recombinant poke-weed antiviral protein and the α-sarcin/ricin stem loop of ribosomal RNA. Journal of Biological Chemistry, 276(26): 24075-24081.
- Ready M.P., Brown D.T., Robertus J.D., 1986. Extracellular localization of pokeweed antiviral protein. Proceedings of the National Academy of Sciences of the United States of America, 83(14): 5053-5056, doi: 10.1073/pnas.83.14.5053.
- Reisfeld R.A., Börjeson J., Chessin L.N., Small Jr. P.A., 1967. Isolation and characterization of a mitogen from pokeweek (Phytolacca americana). Proceedings of the National Academy of Sciences of the United States of America, 58(5): 2020-2027, doi: 10.1073/pnas.58.5.2020.
- Riveiro S.F., Cruz Ó., Reyes O., 2024. Are the invasive Acacia melanoxylon and Eucalyptus globulus drivers of other species invasion? Testing their allelochemical effects on germination. New Forests, 55(4): 751-767, doi: 10.1007/s11056-023-10001-1.
- ROZPORZĄDZENIE WYKONAWCZE KOMISJI (UE) 2016/1141 z dnia 13 lipca 2016 r. przyjmujące wykaz inwazyjnych gatunków obcych uznanych za stwarzające zagrożenie dla Unii zgodnie z rozporządzeniem Parlamentu Europejskiego i Rady (UE) nr 1143/2014 [Commission Implementing Regulation (EU) 2016/1141 of 13 July 2016 adopting a list of invasive alien species of Union concern pursuant to Regulation (EU) No 1143/2014 of the European Parliament and of the Council 9 https://eur-lex.europa.eu/eli/reg_impl/2016/1141/oj/eng)] + regulacje z 12.07.2017, 25.07.2019, 12.07.2022 ( https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:02016R1141-20220802&from=EN).
- Saleri F.D., Chen G., Li X., Guo M., 2017. Comparative analysis of saponins from different Phytolaccaceae species and their antiproliferative activities. Molecules, 22(7), art. no. 1077.
- Sato D., Shimizu N., Shimizu Y., Akagi M., Eshita Y., Ozaki S.-I., Nakajima N., Ishihara K., Masuoka N., Hamada H., Shimoda K., Kubota N., 2014. Synthesis of glycosides of resveratrol, pterostilbene, and piceatannol, and their anti-oxidant, anti-allergic, and neuroprotective activities. Bioscience, Biotechnology and Biochemistry, 78(7): 1123-1128, doi: 10.1080/09168451.2014.921551.
- Schönfelder M., Janott U., Frötschl R., Mundry K.-W., Adam G., 1992. Purification of antiviral proteins with ribosomeinactivating properties from plants. Zeitschrift fur Naturforschung - Section C Journal of Biosciences, 47(9-10): 731-738, doi: 10.1515/znc-1992-9-1016.
- Shahin-Kaleybar B., Niazi A., Afsharifar A., Nematzadeh G., Yousefi R., Retzl B., Hellinger R., Muratspahić E., Gruber C.W., 2020. Isolation of cysteine-rich peptides from Citrullus colocynthis. Biomolecules, 10(9), art. no. 1326, pp. 1-17, doi: 10.3390/biom10091326.
- Shimada S., Otsuki H., Sakuta M., 2007. Transcriptional control of anthocyanin biosynthetic genes in the Caryophyllales. Journal of Experimental Botany, 58(5): 957-967, doi: 10.1093/jxb/erl256.
- Shimada S., Inoue Y.T., Sakuta M., 2005. Anthocyanidin synthase in non-anthocyanin-producing caryophyllales species. Plant Journal, 44(6): 950-959.
- Shimoda K., Kubota N., Hamada H., Doi S., Ishihara K., Hamada H., Fujitaka Y., Ono T., Araki M., 2018. Ferulic acid, methyl ferulate, and ferulic acid glucopyranosyl ester isolated from cultured cells of phytolacca Americana. Natural Product Communications, 13(1): 67-68, doi: 10.1177/1934578x1801300120.
- Shimoda K., Kubota N., Hamada H., Hamada H., 2015a. Synthesis of Resveratrol Glycosides by Plant Glucosyltransferase and Cyclodextrin Glucanotransferase and Their Neuroprotective Activity. Natural Product Communications, 10(6), doi: 10.1177/1934578X1501000649.
- Shimoda K., Kubota N., Hirano H., Matsumoto M., Hamada H., Hamada H., 2012. Formation of tetrahydrocurcumin by reduction of curcumin with cultured plant cells of Marchantia polymorpha. Natural Product Communications, 7(4): 529-530, doi: 10.1177/1934578x1200700428.
- Shimoda K., Kubota N., Okada S., Doi S., Uesugi D., Hamada H., Hamada H., Kuboki A., Iwaki T., Kiriake Y., Saikawa T., Ishihara K., 2019a. Glycosylation of piceid and resveratroloside by bioconversion with Phytolacca americana glucosyltransferase expressed in Escherichia coli. Natural Product Communications, 14(7), doi: 10.1177/1934578X19863519.
- Shimoda K., Kubota N., Uesugi D., Fujitaka Y., Okada S., Tanigawa M., Hamada H., 2015b. Regioselective Glycosylation of 3-, 5-, 6-, and 7-Hydroxyflavones by Cultured Plant Cells. Natural Product Communications, 10(6), doi: 10.1177/1934578X1501000632.
- Shimoda K., Kubota N., Uesugi D., Hamada H., 2014. Glycosylation of artepillin C with cultured plant cells of Phytolacca americana. Natural Product Communications, 9(5): 683-685, doi: 10.1177/1934578x1400900525.
- Shimoda K., Kubota N., Uesugi D., Kobayashi Y., Hamada H., Hamada H., 2020. Glycosylation of stilbene compounds by cultured plant cells. Molecules, 25(6), art. no. 1437, doi: 10.3390/molecules25061437.
- Shimoda K., Kubota N., Uesugi D., Tanigawa M., Hamada H., 2016. Hydroxylation and glycosylation of phenylpropanoids by cultured cells of Phytolacca americana. Natural Product Communications, 11(2): 197-198, doi: 10.1177/1934578x1601100216.
- Shimoda K., Ono T., Hamada H., 2021. Regioselective hydroxylation and dehydrogenation of capsaicin and dihydrocapsaicin by cultured cells of Phytolacca americana. Bioscience, Biotechnology and Biochemistry, 85(1): 103-107, doi: 10.1093/bbb/zbaa004.
- Shimoda K., Kubota N., Uesugi D., Fujitaka Y., Doi S., Hamada H., Kuboki A., Kiriake Y., Iwaki T., Saikawa T., Ozaki S., 2019b. Synthesis of Glycosides of Resveratrol, Pinostilbene, and Piceatannol by Bioconversion with Phytolacca americana. Natural Product Communications, 14(8).
- Sipahioğlu H.M., Kaya İ., Usta M., Ünal M., Özcan D., Özer M., Güller A., Pallas V., 2017. Pokeweed (Phytolacca americana L.) antiviral protein inhibits zucchini yellow mosaic virus infection in a dose-dependent manner in squash plants. Turkish Journal of Agriculture and Forestry, 41(4): 256-262, doi: 10.3906/tar-1612-30.
- Smirnov S., Shulaev V., Tumer N.E., 1997. Expression of poke-weed antiviral protein in transgenic plants induces virus resistance in grafted wild-type plants independently of salicylic acid accumulation and pathogenesis-related protein synthesis. Plant Physiology, 114(3): 1113-1121.
- Stirpe F., Barbieri L., Gorini P., Valbonesi P., Bolognesi A., Polito L., 1996. Activities associated with the presence of ribosome-inactivating proteins increase in senescent and stressed leaves. FEBS Letters, 382(3): 309-312.
- Strgulc Krajšek S., Kladnik A., Skočir S., Bačič M., 2023. Seed germination of invasive Phytolacca americana and potentially invasive P. acinosa. Plants, 12(5), art. no. 1052, doi: 10.3390/plants12051052.
- Suga Y., Maruyama Y., Kawanishi S., Shoji J., 1978. Studies on the Constituents of Phytolaccaceous Plants. II). On the Structures of Phytolaccasaponin B, E and G from the Roots of Phytolacca americana L. Chemical and Pharmaceutical Bulletin, 26(2): 520-525, doi: 10.1248/cpb.26.520.
- Suzuki T., Iwabuchi N., Tokuda R., Matsumoto O., Yoshida T., Nishikawa M., Maejima K., Namba S., Yamaji Y., 2021. Complete Genome Sequence of Mirabilis Crinkle Mosaic Virus Isolated from Pokeweed in Japan. Microbiology Resource Announcements, 10(21).
- Święcicki W.K., Surma M., 2021. The big five in the world of plants – the species that have changed the course of history Polish Journal of Agronomy, 47: 68-77, doi: 10.26114/pja. iung.456.2021.47.
- Takahashi H., Namikawa Y., Tanaka M., Fukuyama Y., 2001. Triterpene glycosides from the cultures of Phytolacca americana. Chemical and Pharmaceutical Bulletin, 49(2): 246-248, doi: 10.1248/cpb.49.246.
- Takahashi K., Takamura E., Sakuta M., 2009. Isolation and expression analysis of two DOPA dioxygenases in Phytolacca americana. Zeitschrift fur Naturforschung - Section C Journal of Biosciences, 64(7-8): 564-573, doi: 10.1515/znc-2009-7-816.
- Takahashi K., Yoshida K., Sakuta M., 2015b. Comparative analysis of two DOPA dioxygenases from Phytolacca americana. Natural Product Communications, 10(5): 713-716, doi: 10.1177/1934578x1501000504.
- Takahashi K., Yoshida K., Yura K., Ashihara H., Sakuta M., 2015a. Biochemical analysis of Phytolacca DOPA dioxygenase. Natural Product Communications, 10(5): 717-719, DOI: 10.1177/1934578x1501000505
- Takahasi H., Yanagi K., Ueda M., Nakade K., Fukuyama Y., 2003. Structures of 1,4-benzodioxane derivatives from the seeds of Phytolacca americana and their neuritogenic activity in primary cultured rat cortical neurons. Chemical and Pharmaceutical Bulletin, 51(12): 1377-1381, doi: 10.1248/cpb.51.1377.
- Tanaka H., Kato I., Ito K., 1987. Total Synthesis of Neolignans, Americanin A and Isoamericanin A. Chemical and Pharmaceutical Bulletin, 35(9): 3603-3608, doi: 10.1248/cpb.35.3603.
- Taylor B.E., Irvin J.D., 1990. Depurination of plant ribosomes by pokeweed antiviral protein. FEBS Letters, 273(1-2): 144-146, doi: 10.1016/0014-5793(90)81070-5.
- Tomlinson J.A., Walker V.M., Flewett T.H., Barclay G.R., 1974. The inhibition of infection by cucumber mosaic virus and influenza virus by extracts from Phytolacca americana. Journal of General Virology, 22(2): 225-232, doi: 10.1099/0022-1317-22-2-225.
- Tourlakis M.E., Karran R.A., Desouza L., Siu K.W., Hudak K.A., 2010. Homodimerization of pokeweed antiviral protein as a mechanism to limit depurination of pokeweed ribosomes. Molecular Plant Pathology, 11(6): 757-767, doi: 10.1111/j.1364-3703.2010.00640.x.
- Trunjaruen A., Luecha P., Taratima W., 2022. Micropropagation of pokeweed (Phytolacca americana L.) and comparison of phenolic, flavonoid content, and antioxidant activity between pokeweed callus and other parts. PeerJ, 10, art. no. e12892, doi: 10.7717/peerj.12892 Tailandia.
- Trunjaruen A., Luecha P., Taratima W., 2023. The optimization of medium conditions and auxins in the induction of adventitious roots of pokeweed (Phytolacca americana L.) and their phytochemical constituents. Scientifica, 2023, art. no. 2983812, doi: 10.1155/2023/2983812.
- Tumer N.E., Hwang D.J., Bonness M., 1997. C-terminal deletion mutant of pokeweed antiviral protein inhibits viral infection but does not depurinate host ribosomes. Proceedings of The National Academy of Sciences of The United States of America, 94(8): 3866-3871.
- Uchikoba T., Yonezawa H., Shimada M., Kaneda M., 1998. Comparison of phytolacain G, a cysteine protease from fruit of Phytolacca americana, with phytolacain R. Bioscience, Biotechnology and Biochemistry, 62 (10), pp. 2058-2061, doi: 10.1271/bbb.62.2058.
- Uesugi D., Hamada H., Shimoda K., Kubota N., Ozaki S.-I., Nagatani N., 2017. Synthesis, oxygen radical absorbance capacity, and tyrosinase inhibitory activity of glycosides of resveratrol, pterostilbene, and pinostilbene. Bioscience, Biotechnology and Biochemistry, 81(2): 226-230, doi: 10.1080/09168451.2016.1240606.
- Ukita M., Furuya A., Tanaka H., Misawa M., 1973. 5′-phosphodiesterase formation by cultured plant cells. Agricultural and Biological Chemistry, 37(12): 2849-2854, doi: 10.1271/bbb1961.37.2849.
- Verloove F., 2013. New xenophytes from Gran Canaria (Canary Islands, Spain), with emphasis on naturalized and (potentially) invasive species. Collectanea Botanica, 32: 59-82, doi: 10.3989/collectbot.2013.v32.006.
- Verloove F., 2017. New xenophytes from the Canary Islands (Gran Canaria and Tenerife Spain). Acta Botanica Croatica, 76(2): 120-131, doi: 10.1515/botcro-2017-0013.
- Wang G., Zhang S., Yao P., Chen Y., Xu X., Li T., Gong G., 2018. Removal of Pb(II) from aqueous solutions by Phytolacca americana L. biomass as a low cost biosorbent. Arabian Journal of Chemistry, 11(1): 99-110, doi: 10.1016/j.arabjc.2015.06.011.
- Wang P., Tumer N.E., 1999. Pokeweed antiviral protein cleaves double-stranded supercoiled DNA using the same active site required to depurinate rRNA. Nucleic Acids Research, 27(8): 1900-1905, doi: 10.1093/nar/27.8.1900.
- Wang S., Wang J., Li J., Hou Y., Shi L., Lian C., Shen Z., Chen Y., 2021. Evaluation of biogas production potential of trace element-contaminated plants via anaerobic digestion. Ecotoxicology and Environmental Safety, 208, art. no. 111598, doi: 10.1016/j.ecoenv.2020.111598.
- Wang X.Y., Cao Y.T., Jin Y., Sun L., Tang F., Dong L.J., 2024a. Ecophysiological trade-off strategies of three gramineous crops in response to root extracts of Phytolacca americana. PLANTS-BASEL, 13(21), 3026, doi: 10.3390/plants13213026.
- Wang T., Li H., Yang X., Zhang Z., Liu S., Yang J., Lu H., Li S., Li M., Guo X., Li Y., 2024b. Exotic plantations differ in “nursing” an understory invader: A probe into invasional meltdown. Ecology and Evolution, 14(5), art. no. e11398, doi: 10.1002/ece3.11398.
- Watanabe K., Kawasaki T., Sako N., Funatsu G., 1997. Actions of pokeweed antiviral protein on virus-infected protoplasts. Bioscience, Biotechnology and Biochemistry, 61(6): 994-997, doi: 10.1271/bbb.61.994.
- Xu Y., Ye X., Yang Q., Weng H., Liu Y., Ahmad S., Zhang G., Huang Q., Zhang T., Liu B., 2023. Ecological niche shifts affect the potential invasive risk of Phytolacca americana (Phytolaccaceae) in China. Ecological Processes, 12(1), art. no. 1, doi: 10.1186/s13717-022-00414-9.
- Xue J., Zhong H., Wang S., Li C., Li J., Wu F., 2016. Kinetics of reduction leaching of manganese dioxide ore with Phytolacca americana in sulfuric acid solution Kinetics of reduction leaching of manganese dioxide ore. Journal of Saudi Chemical Society, 20(4): 437-442, doi: 10.1016/j.jscs.2014.09.011.
- Yamagami T., Tanigawa M., Ishiguro M., Funatsu G., 1998. Complete amino acid sequence of chitinase-a from leaves of pokeweed (Phytolacca americana). Bioscience, Biotechnology and Biochemistry, 62(4): 825-828, doi: 10.1271/bbb.62.825.
- Yamaguchi K., Uechi M., Katakura Y., Oda T., Ishiguro M., 2004. Mitogenic properties of pokeweed lectin-D isoforms on human peripheral blood lymphocytes: Non-mitogen PLD1 and mitogen PL-D2. Bioscience, Biotechnology and Biochemistry, 68(7): 1591-1593, doi: 10.1271/bbb.68.1591.
- Yamaguchi K.-I., Mori A., Funatsu G., 1996. Amino acid sequence and some properties of lectin-d from the roots of pokeweed (Phytolacca americana). Bioscience, Biotechnology and Biochemistry, 60(8): 1380-1382, doi: 10.1271/bbb.60.1380.
- Yamaguchi K.-I., Yurino N., Kino M., Ishiguro M., Funatsu G., 1997. The amino acid sequence of mitogenic lectin-b from the roots of pokeweed (Phytolacca americana). Bioscience, Biotechnology and Biochemistry, 61(4): 690-698, doi: 10.1271/bbb.61.690.
- Yang J.S., Kim H.J., Ryu Y.H., Yun C.-H., Chung D.K., Han S.H., 2006. Endotoxin contamination in commercially available pokeweed mitogen contributes to the activation of murine macrophages and human dendritic cell maturation. Clinical and Vaccine Immunology, 13(3): 309-313, doi: 10.1128/CVI.13.3.309-313.2006.
- Yang W.-H., Wieczorck M., Allen M.C., Nett T.M., 2003. Cytotoxic activity of gonadotropin-releasing hormone (GnRH)-pokeweed antiviral protein conjugates in cell lines expressing GnRH receptors. Endocrinology, 144(4): 1456-1463, doi: 10.1210/en.2002-220917.
- Yasukawa R., Moriwaki N., Uesugi D., Kaneko F., Hamada H., Ozaki S.-I., 2015. Enzymatic synthesis of quercetin monoglucopyranoside and maltooligosaccharides. Natural Product Communications, 10(6), doi: 10.1177/1934578X 1501000639
- Yazlık A., Ambarlı D., 2022. Do non-native and dominant native species carry a similar risk of invasiveness? A case study for plants in Turkey. NeoBiota, 76: 53-72, doi: 10.3897/neo-biota.76.85973.
- Yu H., Gong L., Wang X., Wu H., Zhao T., Wang K., Cui X., Chen L., 2016. Rabbit conjunctivae edema and release of NO, TNF-α, and IL-1β from macrophages induced by fractions and esculentosides isolated from Phytolacca americana. Pharmaceutical Biology, 54(1): 98-104, doi: 10.3109/13880209.2015.1016182.
- Zhabokritsky A., Mansouri S., Hudak K.A., 2014. Pokeweed antiviral protein alters splicing of HIV-1 RNAs, resulting in reduced virus production. RNA, 20(8): 1238-1247, doi: 10.1261/rna.043141.113.
- Zhao H., Wei Y., Wang J., Chai T., 2019. Isolation and expression analysis of cadmium-induced genes from Cd/Mn hyperaccumulator Phytolacca americana in response to high Cd exposure. Plant Biology, 21(1): 15-24, doi: 10.1111/plb.12908.
- Zhao L., Zhu Y.-H., Wang M., Ma L.-G., Han Y.-G., Zhang M.-J., Li X.-C., Feng W.-S., Zheng X.-K., 2021. Comparative transcriptome analysis of the hyperaccumulator plant Phytolacca americana in response to cadmium stress. 3 Biotech, 11(7), art. no. 327, doi: 10.1007/s13205-021-02865-x.
- Zheleva-Dimitrova D.Z., 2013. Antioxidant and acetylcholinesterase inhibition properties of Amorpha fruticosa L. and Phytolacca americana L. Pharmacognosy Magazine, 9(34): 109-113, doi: 10.4103/0973-1296.111251.
- Zhou Y., Chen C., Xiong Y., Xiao F., Wang Y., 2023. Heavy metal induced resistance to herbivore of invasive plant: implications from inter- and intraspecific comparisons. Frontiers in Plant Science, 14, art. no. 1222867, doi: 10.3389/fpls.2023.1222867.
- Zima D., Stefanic E., 2021. Invasive vascular flora of Pozega Valley, Republic of Croatia: diversity and risk assessment. Zbornik Veleucilista u Rijeci-Journal of the Polytechnics of Rijeka, 9(1): 441-451.