1.
Kliebenstein DJ: Secondary metabolites and plant/environment interactions: a view through Arabidopsis
thaliana tinged glasses. Plant, Cell & Environment 2004, 27(6):675-684.
2.
Yang L, Wen K-S, Ruan X, Zhao Y-X, Wei F, Wang Q: Response of Plant Secondary Metabolites to Environmental Factors. Molecules (Basel, Switzerland) 2018, 23(4):762.
3.
D'Auria JC, Gershenzon J: The secondary metabolism of Arabidopsis thaliana: growing like a weed. Current opinion in plant biology 2005, 8(3):308-316.
4.
Dixon RA, Paiva NL: Stress-Induced Phenylpropanoid Metabolism. The Plant cell 1995, 7(7):1085-1097.
5.
Kefeli VI, Kalevitch M, Borsari B: Phenolic cycle in plants and environment. Journal of Cell and Molecular Biology 2003, 2:13-18.
6.
Klessig DF, Choi HW, Dempsey DA: Systemic Acquired Resistance and Salicylic Acid: Past, Present, and Future. Molecular plant-microbe interactions : MPMI 2018, 31(9):871-888.
7.
He XZ, Dixon RA: Genetic manipulation of isoflavone 7-O-methyltransferase enhances biosynthesis of
4'-O-methylated isoflavonoid phytoalexins and disease resistance in alfalfa. The Plant cell 2000, 12(9):1689-1702.
8.
Rice-Evans C, Miller N, Paganga G: Antioxidant properties of phenolic compounds. Trends in plant science 1997, 2(4):152-159.
9.
Gnonlonfin GJB, Sanni A, Brimer L: Review Scopoletin – A Coumarin Phytoalexin with Medicinal Properties. Critical Reviews in Plant Sciences 2012, 31(1):47-56.
10.
Mierziak J, Kostyn K, Kulma A: Flavonoids as important molecules of plant interactions with the environment. Molecules (Basel, Switzerland) 2014, 19(10):16240-16265.
11.
Liu X, Lin C, Ma X, Tan Y, Wang J, Zeng M: Functional Characterization of a Flavonoid Glycosyltransferase in Sweet Orange (Citrus
sinensis). Frontiers in plant science 2018, 9:166.
12.
Baidez AG, Gomez P, Del Rio JA, Ortuno A: Dysfunctionality of the xylem in Olea europaea L. Plants associated with the infection
process by Verticillium dahliae Kleb. Role of phenolic compounds in plant defense
mechanism. Journal of agricultural and food chemistry 2007, 55(9):3373-3377.
13.
El Hadrami A, Adam LR, Daayf F: Biocontrol treatments confer protection against Verticillium dahliae infection of
potato by inducing antimicrobial metabolites. Molecular plant-microbe interactions : MPMI 2011, 24(3):328-335.
14.
Hernandez I, Alegre L, Van Breusegem F, Munne-Bosch S: How relevant are flavonoids as antioxidants in plants? Trends in plant science 2009, 14(3):125-132.
15.
Agati G, Azzarello E, Pollastri S, Tattini M: Flavonoids as antioxidants in plants: location and functional significance. Plant science : an international journal of experimental plant biology 2012, 196:67-76.
16.
Wang J, Hou B: Glycosyltransferases: key players involved in the modification of plant secondary
metabolites. Frontiers of Biology in China 2009, 4(1):39-46.
17.
Bowles D, Isayenkova J, Lim EK, Poppenberger B: Glycosyltransferases: managers of small molecules. Curr Opin Plant Biol 2005, 8(3):254-263.
18.
Lim EK, Bowles DJ: A class of plant glycosyltransferases involved in cellular homeostasis. The EMBO journal 2004, 23(15):2915-2922.
19.
Gachon CM, Langlois-Meurinne M, Saindrenan P: Plant secondary metabolism glycosyltransferases: the emerging functional analysis. Trends in plant science 2005, 10(11):542-549.
20.
Ghose K, Selvaraj K, McCallum J, Kirby CW, Sweeney-Nixon M, Cloutier SJ, Deyholos
M, Datla R, Fofana B: Identification and functional characterization of a flax UDP-glycosyltransferase glucosylating
secoisolariciresinol (SECO) into secoisolariciresinol monoglucoside (SMG) and diglucoside
(SDG). BMC plant biology 2014, 14:82.
21.
Li Y, Baldauf S, Lim EK, Bowles DJ: Phylogenetic analysis of the UDP-glycosyltransferase multigene family of Arabidopsis
thaliana. The Journal of biological chemistry 2001, 276(6):4338-4343.
22.
Vogt T, Jones P: Glycosyltransferases in plant natural product synthesis: characterization of a supergene
family. Trends in plant science 2000, 5(9):380-386.
23.
Brazier-Hicks M, Offen WA, Gershater MC, Revett TJ, Lim EK, Bowles DJ, Davies GJ,
Edwards R: Characterization and engineering of the bifunctional N- and O-glucosyltransferase
involved in xenobiotic metabolism in plants. Proceedings of the National Academy of Sciences of the United States of America 2007, 104(51):20238-20243.
24.
Modolo LV, Li L, Pan H, Blount JW, Dixon RA, Wang X: Crystal structures of glycosyltransferase UGT78G1 reveal the molecular basis for glycosylation
and deglycosylation of (iso)flavonoids. Journal of molecular biology 2009, 392(5):1292-1302.
25.
Cartwright AM, Lim E-K, Kleanthous C, Bowles DJ: A kinetic analysis of regiospecific glucosylation by two glycosyltransferases of Arabidopsis
thaliana: domain swapping to introduce new activities. The Journal of biological chemistry 2008, 283(23):15724-15731.
26.
Werner SR, Morgan JA: Controlling selectivity and enhancing yield of flavonoid glycosides in recombinant
yeast. Bioprocess and biosystems engineering 2010, 33(7):863-871.
27.
Davies GJ, Gloster TM, Henrissat B: Recent structural insights into the expanding world of carbohydrate-active enzymes. Current opinion in structural biology 2005, 15(6):637-645.
28.
Le Roy J, Huss B, Creach A, Hawkins S, Neutelings G: Glycosylation Is a Major Regulator of Phenylpropanoid Availability and Biological
Activity in Plants. Frontiers in plant science 2016, 7:735.
29.
Lim EK, Doucet CJ, Li Y, Elias L, Worrall D, Spencer SP, Ross J, Bowles DJ: The activity of Arabidopsis glycosyltransferases toward salicylic acid, 4-hydroxybenzoic
acid, and other benzoates. The Journal of biological chemistry 2002, 277(1):586-592.
30.
Chong J, Baltz R, Schmitt C, Beffa R, Fritig B, Saindrenan P: Downregulation of a pathogen-responsive tobacco UDP-Glc:phenylpropanoid glucosyltransferase
reduces scopoletin glucoside accumulation, enhances oxidative stress, and weakens
virus resistance. The Plant cell 2002, 14(5):1093-1107.
31.
Gachon C, Baltz R, Saindrenan P: Over-expression of a scopoletin glucosyltransferase in Nicotiana tabacum leads to
precocious lesion formation during the hypersensitive response to tobacco mosaic virus
but does not affect virus resistance. Plant molecular biology 2004, 54(1):137-146.
32.
Langenbach C, Campe R, Schaffrath U, Goellner K, Conrath U: UDP-glucosyltransferase UGT84A2/BRT1 is required for Arabidopsis nonhost resistance
to the Asian soybean rust pathogen Phakopsora pachyrhizi. New Phytologist 2013, 198(2):536-545.
33.
Simon C, Langlois-Meurinne M, Didierlaurent L, Chaouch S, Bellvert F, Massoud K, Garmier
M, Thareau V, Comte G, Noctor G et al: The secondary metabolism glycosyltransferases UGT73B3 and UGT73B5 are components of
redox status in resistance of Arabidopsis to Pseudomonas syringae pv. tomato. Plant Cell Environ 2014, 37(5):1114-1129.
34.
Song C, Gu L, Liu J, Zhao S, Hong X, Schulenburg K, Schwab W: Functional Characterization and Substrate Promiscuity of UGT71 Glycosyltransferases
from Strawberry (Fragaria x ananassa). Plant & cell physiology 2015, 56(12):2478-2493.
35.
Tárraga S, Lisón P, López-Gresa MP, Torres C, Rodrigo I, Bellés JM, Conejero V: Molecular cloning and characterization of a novel tomato xylosyltransferase specific
for gentisic acid. Journal of experimental botany 2010, 61(15):4325-4338.
36.
von Saint Paul V, Zhang W, Kanawati B, Geist B, Faus-Kessler T, Schmitt-Kopplin P,
Schaffner AR: The Arabidopsis glucosyltransferase UGT76B1 conjugates isoleucic acid and modulates
plant defense and senescence. The Plant cell 2011, 23(11):4124-4145.
37.
Kim JH, Kim BG, Ko JH, Lee Y, Hur H-G, Lim Y, Ahn J-H: Molecular cloning, expression, and characterization of a flavonoid glycosyltransferase
from Arabidopsis thaliana. Plant Science 2006, 170(4):897-903.
38.
Griesser M, Vitzthum F, Fink B, Bellido ML, Raasch C, Munoz-Blanco J, Schwab W: Multi-substrate flavonol O-glucosyltransferases from strawberry (Fragaria x ananassa)
achene and receptacle. Journal of experimental botany 2008, 59(10):2611-2625.
39.
Rehman HM, Nawaz MA, Shah ZH, Ludwig-Müller J, Chung G, Ahmad MQ, Yang SH, Lee SI:
Comparative genomic and transcriptomic analyses of Family-1 UDP glycosyltransferase
in three Brassica species and Arabidopsis indicates stress-responsive regulation. Scientific Reports 2018, 8(1):1875.
40.
O'Donnell PJ, Truesdale MR, Calvert CM, Dorans A, Roberts MR, Bowles DJ: A novel tomato gene that rapidly responds to wound- and pathogen-related signals. The Plant Journal 1998, 14(1):137-142.
41.
Horvath DM, Chua NH: Identification of an immediate-early salicylic acid-inducible tobacco gene and characterization
of induction by other compounds. Plant molecular biology 1996, 31(5):1061-1072.
42.
Fraissinet-Tachet L, Baltz R, Chong J, Kauffmann S, Fritig B, Saindrenan P: Two tobacco genes induced by infection, elicitor and salicylic acid encode glucosyltransferases
acting on phenylpropanoids and benzoic acid derivatives, including salicylic acid. FEBS letters 1998, 437(3):319-323.
43.
Langlois-Meurinne M, Gachon CMM, Saindrenan P: Pathogen-responsive expression of glycosyltransferase genes UGT73B3 and UGT73B5 is
necessary for resistance to Pseudomonas syringae pv tomato in Arabidopsis. Plant physiology 2005, 139(4):1890-1901.
44.
Lee BJ, Kim SK, Choi SB, Bae J, Kim KJ, Kim YJ, Paek KH: Pathogen-inducible CaUGT1 is involved in resistance response against TMV infection
by controlling salicylic acid accumulation. FEBS letters 2009, 583(13):2315-2320.
45.
Lee HI, Raskin I: Purification, cloning, and expression of a pathogen inducible UDP-glucose:Salicylic
acid glucosyltransferase from tobacco. The Journal of biological chemistry 1999, 274(51):36637-36642.
46.
Taguchi G, Imura H, Maeda Y, Kodaira R, Hayashida N, Shimosaka M, Okazaki M: Purification and characterization of UDP-glucose: hydroxycoumarin 7-O-glucosyltransferase,
with broad substrate specificity from tobacco cultured cells. Plant science : an international journal of experimental plant biology 2000, 157(1):105-112.
47.
Jackson RG, Lim EK, Li Y, Kowalczyk M, Sandberg G, Hoggett J, Ashford DA, Bowles DJ:
Identification and biochemical characterization of an Arabidopsis indole-3-acetic
acid glucosyltransferase. The Journal of biological chemistry 2001, 276(6):4350-4356.
48.
Isayenkova J, Wray V, Nimtz M, Strack D, Vogt T: Cloning and functional characterisation of two regioselective flavonoid glucosyltransferases
from Beta vulgaris. Phytochemistry 2006, 67(15):1598-1612.
49.
Seto Y, Hamada S, Matsuura H, Matsushige M, Satou C, Takahashi K, Masuta C, Ito H,
Matsui H, Nabeta K: Purification and cDNA cloning of a wound inducible glucosyltransferase active toward
12-hydroxy jasmonic acid. Phytochemistry 2009, 70(3):370-379.
50.
Li X, Svedin E, Mo H, Atwell S, Dilkes BP, Chapple C: Exploiting natural variation of secondary metabolism identifies a gene controlling
the glycosylation diversity of dihydroxybenzoic acids in Arabidopsis thaliana. Genetics 2014, 198(3):1267-1276.
51.
Dewitte G, Walmagh M, Diricks M, Lepak A, Gutmann A, Nidetzky B, Desmet T: Screening of recombinant glycosyltransferases reveals the broad acceptor specificity
of stevia UGT-76G1. Journal of biotechnology 2016, 233:49-55.
52.
Garcia D, Sanier C, Macheix JJ, D'Auzac J: Accumulation of scopoletin in Hevea brasiliensis infected by Microcyclus ulei (P.
Henn.) V. ARX and evaluation of its fungitoxicity for three leaf pathogens of rubber
tree. Physiological and Molecular Plant Pathology 1995, 47(4):213-223.
53.
Baillieul F, de Ruffray P, Kauffmann S: Molecular cloning and biological activity of alpha-, beta-, and gamma-megaspermin,
three elicitins secreted by Phytophthora megasperma H20. Plant physiology 2003, 131(1):155-166.
54.
Shimizu B, Miyagawa H, Ueno T, Sakata K, Watanabe K, Ogawa K: Morning glory systemically accumulates scopoletin and scopolin after interaction with
Fusarium oxysporum. Zeitschrift fur Naturforschung C, Journal of biosciences 2005, 60(1-2):83-90.
55.
Ogawa K: Studies on Fusarium wilt of sweet potato (Ipomoea batatas L.). Bulletin of the National Agricultural Research Center, Japan 1988, 10:127-161.
56.
Tanguy J, Martin C: Phenolic compounds and the hypersensitivity reaction in nicotiana tabacum infected
with tobacco mosaic virus. Phytochemistry 1972, 11(1):19-28.
57.
Churngchow N, Rattarasarn M: The elicitin secreted by Phytophthora palmivora, a rubber tree pathogen. Phytochemistry 2000, 54(1):33-38.
58.
Goy PA, Signer H, Reist R, Aichholz R, Blum W, Schmidt E, Kessmann H: Accumulation of scopoletin is associated with the high disease resistance of the hybrid
Nicotiana glutinosa x Nicotiana debneyi. Planta 1993, 191(2):200-206.
59.
Sun H, Wang L, Zhang B, Ma J, Hettenhausen C, Cao G, Sun G, Wu J, Wu J: Scopoletin is a phytoalexin against Alternaria alternata in wild tobacco dependent
on jasmonate signalling. Journal of experimental botany 2014, 65(15):4305-4315.
60.
Kai K, Shimizu B, Mizutani M, Watanabe K, Sakata K: Accumulation of coumarins in Arabidopsis thaliana. Phytochemistry 2006, 67(4):379-386.
61.
Sim M-O, Lee H-I, Ham JR, Seo K-I, Lee M-K: Long-term supplementation of esculetin ameliorates hepatosteatosis and insulin resistance
partly by activating AdipoR2–AMPK pathway in diet-induced obese mice. Journal of Functional Foods 2015, 15:160-171.
62.
Mazimba O: Umbelliferone: Sources, chemistry and bioactivities review. Bulletin of Faculty of Pharmacy, Cairo University 2017, 55(2):223-232.
63.
Carpinella MC, Ferrayoli CG, Palacios SM: Antifungal synergistic effect of scopoletin, a hydroxycoumarin isolated from Melia
azedarach L. fruits. Journal of agricultural and food chemistry 2005, 53(8):2922-2927.
64.
Chen T, Guo Q, Wang H, Zhang H, Wang C, Zhang P, Meng S, Li Y, Ji H, Yan T: Effects of esculetin on lipopolysaccharide (LPS)-induced acute lung injury via regulation
of RhoA/Rho Kinase/NF-small ka, CyrillicB pathways in vivo and in vitro. Free radical research 2015, 49(12):1459-1468.
65.
Prabakaran D, Ashokkumar N: Protective effect of esculetin on hyperglycemia-mediated oxidative damage in the hepatic
and renal tissues of experimental diabetic rats. Biochimie 2013, 95(2):366-373.
66.
Sheyn U, Rosenwasser S, Ben-Dor S, Porat Z, Vardi A: Modulation of host ROS metabolism is essential for viral infection of a bloom-forming
coccolithophore in the ocean. The ISME journal 2016, 10(7):1742-1754.
67.
Bellés JM, Garro R, Fayos J, Navarro P, Primo J, Conejero V: Gentisic Acid As a Pathogen-Inducible Signal, Additional to Salicylic Acid for Activation
of Plant Defenses in Tomato. Molecular Plant-Microbe Interactions 1999, 12(3):227-235.
68.
Fayos J, Belles JM, Lopez-Gresa MP, Primo J, Conejero V: Induction of gentisic acid 5-O-beta-D-xylopyranoside in tomato and cucumber plants
infected by different pathogens. Phytochemistry 2006, 67(2):142-148.
69.
Bartsch M, Bednarek P, Vivancos PD, Schneider B, von Roepenack-Lahaye E, Foyer CH,
Kombrink E, Scheel D, Parker JE: Accumulation of isochorismate-derived 2,3-dihydroxybenzoic 3-O-beta-D-xyloside in
arabidopsis resistance to pathogens and ageing of leaves. The Journal of biological chemistry 2010, 285(33):25654-25665.
70.
Dachineni R, Kumar DR, Callegari E, Kesharwani SS, Sankaranarayanan R, Seefeldt T,
Tummala H, Bhat GJ: Salicylic acid metabolites and derivatives inhibit CDK activity: Novel insights into
aspirin's chemopreventive effects against colorectal cancer. International journal of oncology 2017, 51(6):1661-1673.
71.
Lorenc-Kukula K, Zuk M, Kulma A, Czemplik M, Kostyn K, Skala J, Starzycki M, Szopa
J: Engineering Flax with the GT Family 1 Solanum sogarandinum Glycosyltransferase SsGT1
Confers Increased Resistance to Fusarium Infection. Journal of agricultural and food chemistry 2009, 57(15):6698-6705.
72.
Song JT, Koo YJ, Seo HS, Kim MC, Choi YD, Kim JH: Overexpression of AtSGT1, an Arabidopsis salicylic acid glucosyltransferase, leads
to increased susceptibility to Pseudomonas syringae. Phytochemistry 2008, 69(5):1128-1134.
73.
Hirade Y, Kotoku N, Terasaka K, Saijo-Hamano Y, Fukumoto A, Mizukami H: Identification and functional analysis of 2-hydroxyflavanone C-glucosyltransferase
in soybean (Glycine max). FEBS letters 2015, 589(15):1778-1786.
74.
Bravo L: Polyphenols: chemistry, dietary sources, metabolism, and nutritional significance. Nutrition reviews 1998, 56(11):317-333.
75.
Ross JA, Kasum CM: Dietary flavonoids: bioavailability, metabolic effects, and safety. Annual review of nutrition 2002, 22:19-34.
76.
Wang Y, Chen S, Yu O: Metabolic engineering of flavonoids in plants and microorganisms. Applied microbiology and biotechnology 2011, 91(4):949-956.
77.
Treutter D: Significance of flavonoids in plant resistance: a review. Environmental Chemistry Letters 2006, 4(3):147.
78.
Bollina V, Kushalappa AC: In vitro inhibition of trichothecene biosynthesis in Fusarium graminearum by resistance-related
endogenous metabolites identified in barley. Mycology 2011, 2(4):291-296.
79.
Bilska K, Stuper-Szablewska K, Kulik T, Busko M, Zaluski D, Jurczak S, Perkowski J:
Changes in Phenylpropanoid and Trichothecene Production by Fusarium culmorum and F.
graminearum Sensu Stricto via Exposure to Flavonoids. Toxins 2018, 10(3).
80.
French CJ, Elder M, Leggett F, Ibrahim RK, Neil Towers GH: Flavonoids inhibit infectivity of tobacco mosaic virus. Canadian Journal of Plant Pathology 1991, 13(1):1-6.
81.
Ko CH, Shen SC, Hsu CS, Chen YC: Mitochondrial-dependent, reactive oxygen species-independent apoptosis by myricetin:
roles of protein kinase C, cytochrome c, and caspase cascade. Biochemical pharmacology 2005, 69(6):913-927.
82.
López-Gresa MP, Torres C, Campos L, Lisón P, Rodrigo I, Bellés JM, Conejero V: Identification of defence metabolites in tomato plants infected by the bacterial pathogen
Pseudomonas syringae. Environmental and Experimental Botany 2011, 74:216-228.
83.
Chitarrini G, Nobili C, Pinzari F, Antonini A, De Rossi P, Del Fiore A, Procacci S,
Tolaini V, Scala V, Scarpari M et al: Buckwheat achenes antioxidant profile modulates Aspergillus flavus growth and aflatoxin
production. International journal of food microbiology 2014, 189:1-10.
84.
Bollina V, Kumaraswamy GK, Kushalappa AC, Choo TM, Dion Y, Rioux S, Faubert D, Hamzehzarghani
H: Mass spectrometry-based metabolomics application to identify quantitative resistance-related
metabolites in barley against Fusarium head blight. Molecular plant pathology 2010, 11(6):769-782.
85.
Gunnaiah R, Kushalappa AC, Duggavathi R, Fox S, Somers DJ: Integrated metabolo-proteomic approach to decipher the mechanisms by which wheat QTL
(Fhb1) contributes to resistance against Fusarium graminearum. PloS one 2012, 7(7):e40695-e40695.
86.
Huang F-C, Giri A, Daniilidis M, Sun G, Härtl K, Hoffmann T, Schwab W: Structural and Functional Analysis of UGT92G6 Suggests an Evolutionary Link Between
Mono- and Disaccharide Glycoside-Forming Transferases. Plant and Cell Physiology 2018, 59(4):862- 875.
87.
Dhaubhadel S, Farhangkhoee M, Chapman R: Identification and characterization of isoflavonoid specific glycosyltransferase and
malonyltransferase from soybean seeds. Journal of experimental botany 2008, 59(4):981-994.
88.
Belles JM, Garro R, Pallas V, Fayos J, Rodrigo I, Conejero V: Accumulation of gentisic acid as associated with systemic infections but not with
the hypersensitive response in plant-pathogen interactions. Planta 2006, 223(3):500-511.
89.
Gu YQ, Yang C, Thara VK, Zhou J, Martin GB: Pti4 is induced by ethylene and salicylic acid, and its product is phosphorylated
by the Pto kinase. The Plant cell 2000, 12(5):771-786.
90.
Ntoukakis V, Mucyn TS, Gimenez-Ibanez S, Chapman HC, Gutierrez JR, Balmuth AL, Jones
AM, Rathjen JP: Host inhibition of a bacterial virulence effector triggers immunity to infection. Science 2009, 324(5928):784-787.
91.
Lopez-Gresa MP, Lison P, Campos L, Rodrigo I, Rambla JL, Granell A, Conejero V, Belles
JM: A Non-targeted Metabolomics Approach Unravels the VOCs Associated with the Tomato
Immune Response against Pseudomonas syringae. Frontiers in plant science 2017, 8:1188.
92.
Soler S, Díez MJ, Roselló S, Nuez F: Movement and distribution of tomato spotted wilt virus in resistant and susceptible
accessions of Capsicum spp. Canadian Journal of Plant Pathology 1999, 21(4):317-325.
93.
Campos L, Granell P, Tarraga S, Lopez-Gresa P, Conejero V, Belles JM, Rodrigo I, Lison
P: Salicylic acid and gentisic acid induce RNA silencing-related genes and plant resistance
to RNA pathogens. Plant Physiology and Biochemistry 2014, 77:35-43.
94.
Nakagawa T, Suzuki T, Murata S, Nakamura S, Hino T, Maeo K, Tabata R, Kawai T, Tanaka
K, Niwa Y et al: Improved Gateway binary vectors: high-performance vectors for creation of fusion constructs
in transgenic analysis of plants. Bioscience, biotechnology, and biochemistry 2007, 71(8):2095-2100.
95.
Helliwell C, Waterhouse P: Constructs and methods for high-throughput gene silencing in plants. Methods (San Diego, Calif) 2003, 30(4):289-295.
96.
Lakatos L, Szittya G, Silhavy D, Burgyan J: Molecular mechanism of RNA silencing suppression mediated by p19 protein of tombusviruses. The EMBO journal 2004, 23(4):876-884.
97.
Ellul P, Garcia-Sogo B, Pineda B, Rios G, Roig LA, Moreno V: The ploidy level of transgenic plants in Agrobacterium-mediated transformation of
tomato cotyledons ( Lycopersicon esculentum Mill.) is genotype and procedure dependent
[corrected]. TAG Theoretical and applied genetics Theoretische und angewandte Genetik 2003, 106(2):231-238.
98.
Yalpani N, Schulz M, Davis MP, Balke NE: Partial purification and properties of an inducible uridine 5'-diphosphate-glucose-salicylic
Acid glucosyltransferase from oat roots. Plant physiology 1992, 100(1):457-463.
99.
Campos L, Lisón P, López-Gresa MP, Rodrigo I, Zacarés L, Conejero V, Bellés JM: Transgenic Tomato Plants Overexpressing Tyramine N-Hydroxycinnamoyltransferase Exhibit
Elevated Hydroxycinnamic Acid Amide Levels and Enhanced Resistance to Pseudomonas
syringae. Molecular Plant-Microbe Interactions 2014, 27(10):1159-1169.
100.
Conejero V, Semancik J: Analysis of the proteins in crude plant extracts by polyacrylamide gel electrophoresis. Phytopathology 1977, 67:1424–1426.
101.
Yalpani N, Leon J, Lawton MA, Raskin I: Pathway of Salicylic Acid Biosynthesis in Healthy and Virus-Inoculated Tobacco. Plant Physiol 1993, 103(2):315-321.
102.
Rambla JL., López-Gresa MP., Bellés JM., A. G: Metabolomic Profiling of Plant Tissues. In: Plant Functional Genomics Methods in Molecular Biology. Edited by Alonso J., A. S, vol. 1284. New York, NY: Humana Press; 2015.