Abstract
Plant transformation protocols generally involve the use of selectable marker genes for the screening of transgenic material. The bacterial gene nptII, coding for a neomycin phosphotransferase, and the hpt gene, coding for a hygromycin phosphotransferase, are frequently used. These enzymes detoxify aminoglycoside antibiotics by phosphorylation, thereby permitting cell growth in the presence of antibiotics. Nevertheless, the screening for transgenic regenerated shoots is often partial and difficult due to regeneration of escapes and chimeras. These difficulties can be caused, in part, by an incorrect assumption about the mode of action of antibiotics in bacterial and eukaryotic cells and in in vitro tissue culture. The information contained in this review could be useful to establish better selection strategies by taking into account factors such as explant complexity, transformation and selection protocols that allow better accessibility to cells of Agrobacterium and antibiotics, and faster regeneration methods that avoid collateral effects of antibiotics on recovered, putative transgenic shoots.
Similar content being viewed by others
References
Ali BH (1995) Gentamicin nephrotoxicity in humans and animals: some recent research. Gen Pharmacol 26:1477–1487. doi:10.1016/0306-3623(95)00049-6
Ballester A, Cervera M, Pena L (2008) Evaluation of selection strategies alternative to NPTII in genetic transformation of citrus. Plant Cell Rep 27:1005–1015. doi:10.1007/s00299-008-0523-z
Brummett R, Fox K (1989) Aminoglycoside-induced hearing loss in humans. Antimicrob Agents Chemother 33:797–800
Bryan LE, Van Den Elzen HM (1975) Gentamicin accumulation by sensitive strains of Escherichia coli and Pseudomonas aeruginosa. J Antibiot 28:696–703
Bryan LE, Van Den Elzen HM (1976) Streptomycin accumulation in susceptible and resistant strains of Escherichia coli and Pseudomonas aeruginosa. Antimicrob Agents Chemother 9:928–938
Buchanan JH, Stevens A, Sidhu J (1987) Aminoglycoside antibiotic treatment of human fibroblasts: intracellular accumulation, molecular changes and the loss of ribosomal accuracy. Eur J Cell Biol 43:141–147
Burgos L, Alburquerque N (2003) Ethylene inhibitors and low kanamycin concentrations improve adventitious regeneration from apricot leaves. Plant Cell Rep 21:1167–1174. doi:10.1007/s00299-003-0625-6
Carrer H, Hockenberry TN, Svab Z, Maliga P (1993) Kanamycin resistance as a selectable marker for plastid transformation in tobacco. Mol Gen Genet 241:49–56
Chauvin JE, Marhadour S, Cohat J, Le Nard M (1999) Effects of gelling agents on in vitro regeneration and kanamycin efficiency as a selective agent in plant transformation procedures. Plant Cell Tissue Organ Cult 58:213–217
Christou P (1990) Morphological description of transgenic soybean chimeras created by the delivery, integration and expression of foreign DNA using electric discharge particle acceleration. Ann Bot 66:379–386
Christou P, Ford TL (1995) Recovery of chimeric rice plants from dry seed using electric discharge particle acceleration. Ann Bot 75:449–454
Colmer TD, Fan TWM (1994) Interactions of Ca2+ and NaCl stress on the ion relations and intracellular pH of Sorghum bicolor root tips: an in vivo 31P NMR study. J Exp Bot 45:1037–1044. doi:10.1093/jxb/45.8.1037
Costa MGC, Otoni WC, Moore GA (2002) An evaluation of factors affecting the efficiency of Agrobacterium-mediated transformation of Citrus paradisi (Macf.) and production of transgenic plants containing carotenoid biosynthetic genes. Plant Cell Rep 21:365–373. doi:10.1007/s00299-002-0533-1
Crawford LM (1972) Calcium inhibition of antibacterial activity of kanamycin. Am J Vet Res 33:1685–1688
Dandekar AM (1992) Transformation. In: Hammerschlag FA, Litz RE (eds) Biotechnology of perennial fruit crops. CAB International, Wallingford, pp 141–168
Daniell H, Muthukumar B, Lee SB (2001) Marker free transgenic plants: engineering the chloroplast genome without the use of antibiotic selection. Curr Genet 39:109–116
Danilova SA, Dolgikh YI (2004) The stimulatory effect of the antibiotic cefotaxime on plant regeneration in maize tissue culture. Russ J Plant Physiol 51:559–562
Davies J, Gorini L, Davis BD (1965) Misreading of RNA codewords induced by aminoglycoside antibiotics. Mol Pharmacol 1:93–106
Davis BD (1988) The lethal action of aminoglycosides. J Antimicrob Chemother 22:1–3
Davis SD, Iannetta A (1972) Antagonistic effect of calcium in serum on activity of tobramycin against Pseudomonas. Antimicrob Agents Chemother 1:466–469
De Ropp RS (1949) The action of antibacterial substances on the growth of Phytomonas tumefaciens and of crown gall tumor tissues. Phytopathol 39:822–828
De Rossi E, Ainsa JA, Riccardi G (2006) Role of mycobacterial efflux transporters in drug resistance: an unresolved question. FEMS Microbiol Rev 30:36–52. doi:10.1111/j.1574-6976.2005.00000.x
Domínguez A, Cervera M, Pérez RM, Romero J, Fagoaga C, Cubero J (2004) Characterisation of regenerants obtained under selective conditions after Agrobacterium-mediated transformation of citrus explants reveals production of silenced and chimeric plants at unexpected high frequencies. Mol Breed 14:171–183
Dong JZ, McHughen A (1993) Transgenic flax plants from Agrobacterium mediated transformation: incidence of chimeric regenerants and inheritance of transgenic plants. Plant Sci 91:139–148
Dubos C, Huggins D, Grant GH, Knight MR, Campbell MM (2003) A role for glycine in the gating of plant NMDA-like receptors. Plant J 35:800–810. doi:10.1046/j.1365-313X.2003.01849.x
Dubos C, Willment J, Huggins D, Grant GH, Campbell MM (2005) Kanamycin reveals the role played by glutamate receptors in shaping plant resource allocation. Plant J 43:348–355. doi:10.1111/j.1365-313X.2005.02458.x
Edelmann P, Gallant J (1977) Mistranslation in E. coli. Cell 10:130–137
Endress V, Barriuso J, Ruperez P, Martin JP, Blazquez A, Villalobos N, Guerra H, Martin L (2009) Differences in cell wall polysaccharide composition between embryogenic and non-embryogenic calli of Medicago arborea L. Plant Cell Tissue Organ Cult 97:323–329. doi:10.1007/s11240-009-9531-0
Epstein E (1961) The essential role of calcium in selective cation transport by plant cells. Plant Physiol 36:437–444
Erikson O, Hertzberg M, Nasholm T (2004) A conditional marker gene allowing both positive and negative selection in plants. Nat Biotechnol 22:455–458. doi:10.1038/nbt946
Faize M, Faize L, Burgos L (2010) Using quantitative real-time PCR to detect chimeras in transgenic tobacco and apricot and to monitor their dissociation (submitted)
Flachowsky H, Riedel M, Reim S, Hanke V (2008) Evaluation of the uniformity and stability of T-DNA integration and gene expression in transgenic apple plants. Electron J Biotechnol 11:1–15. doi:10.2225/vol11-issue1-fulltext-10
Fourmy D, Recht MI, Blanchard SC, Puglisi JD (1996) Structure of the A site of Escherichia coli 16S ribosomal RNA complexed with an aminoglycoside antibiotic. Science 274:1367–1371
Goddijn OJM, Schouten PMV, Schilperoort RA, Hoge JHC (1993) A chimeric tryptophan decarboxylase gene as a novel selectable marker in plant cells. Plant Mol Biol 22:907–912
Gough KC, Hawes WS, Kilpatrick J, Whitelam GC (2001) Cyanobacterial GR6 glutamate-1-semialdehyde aminotransferase: a novel enzyme-based selectable marker for plant transformation. Plant Cell Rep 20:296–300
Grant JE, Cooper PA, Gilpin BJ, Hoglund SJ, Reader JK, Pither-Joyce MD, Timmerman-Vaughan GM (1998) Kanamycin is effective for selecting transformed peas. Plant Sci 139:159–164
Halaban R, Alfano FD (1984) Selective elimination of fibroblasts from cultures of normal human melanocytes. In Vitro 20:447–450
Haldrup A, Petersen SG, Okkels FT (1998) The xylose isomerase gene from Thermoanaerobacterium thermosulfurogenes allows effective selection of transgenic plant cells using D-xylose as the selection agent. Plant Mol Biol 37:287–296
Hancock REW (1981a) Aminoglycoside uptake and mode of action with special reference to streptomycin and gentamicin. 1. Antagonists and mutants. J Antimicrob Chemother 8:249–276
Hancock REW (1981b) Aminoglycoside uptake and mode of action - with special reference to streptomycin and gentamicin. 2. Effects of aminoglycosides on cells. J Antimicrob Chemother 8:429–445
Harvey SC, Skolnick P (1999) Polyamine-like actions of aminoglycosides at recombinant N-methyl-D-aspartate receptors. J Pharmacol Exp Ther 291:285–291
Hauptmann RM, Vasil V, Oziasakins P, Tabaeizadeh Z, Rogers SG, Fraley RT, Horsch RB, Vasil IK (1988) Evaluation of selectable markers for obtaining stable transformants in the Gramineae. Plant Physiol 86:602–606
Haws CM, Winegar BD, Lansman JB (1996) Block of single L-type Ca2+ channels in skeletal muscle fibers by aminoglycoside antibiotics. J Gen Physiol 107:421–432
Herrera-Estrella L, Deblock M, Messens E, Hernalsteens JP, Vanmontagu M, Schell J (1983) Chimeric genes as dominant selectable markers in plant cells. EMBO J 2:987–995
Holford P, Newbury HJ (1992) The effects of antibiotics and their breakdown products on the in vitro growth of Antirrhinum majus. Plant Cell Rep 11:93–96
Hon WC, McKay GA, Thompson PR, Sweet RM, Yang DSC, Wright GD, Berghuis AM (1997) Structure of an enzyme required for aminoglycoside antibiotic resistance reveals homology to eukaryotic protein kinases. Cell 89:887–895
Howard M, Frizzell DM, Bedwell DM (1996) Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations. Nat Med 2:467–469
Jerinic O, Joseph S (2000) Conformational changes in the ribosome induced by translational miscoding agents. J Mol Biol 304:707–713
Jiang H, Sha SH, Schacht J (2006) Kanamycin alters cytoplasmic and nuclear phosphoinositide signaling in the organ of corti in vivo. J Neurochem 99:269–276. doi:10.1111/j.1471-4159.2006.04117.x
Joersbo M, Okkels FT (1996a) A novel principle for selection of transgenic plant cells: positive selection. Plant Cell Rep 16:219–221
Joersbo M, Okkels FT (1996b) Calcium reduces toxicity of aminoglycoside antibiotics in sugar beet explants in vitro. Physiol Plant 97:245–250
Joersbo M, Donaldson I, Kreiberg J, Petersen SG, Brunstedt J, Okkels FT (1998) Analysis of mannose selection used for transformation of sugar beet. Mol Breed 4:111–117
Joersbo M, Jorgensen K, Brunstedt J (2003) A selection system for transgenic plants based on galactose as selective agent and a UDP-glucose: galactose-1-phosphate uridyl-transferase gene as selective gene. Mol Breed 11:315–323
Jordan MC, McHughen A (1988) Transformed callus does not necessarily regenerate transformed shoots. Plant Cell Rep 7:285–287
Keeling KM, Brooks DA, Hopwood JJ, Li PN, Thompson JN, Bedwell DM (2001) Gentamicin-mediated suppression of Hurler syndrome stop mutations restores a low level of alpha-L-iduronidase activity and reduces lysosomal glycosaminoglycan accumulation. Hum Mol Genet 10:291–299
Kunze I, Ebneth M, Heim U, Geiger M, Sonnewald U, Herbers K (2001) 2-Deoxyglucose resistance: a novel selection marker for plant transformation. Mol Breed 7:221–227
Kurtz DI (1974) Fidelity of protein-synthesis with chicken embryo mitochondrial and cytoplasmic ribosomes. Biochemistry 13:572–577
LaFayette PR, Kane PM, Phan BH, Parrott WA (2005) Arabitol dehydrogenase as a selectable marker for rice. Plant Cell Rep 24:596–602. doi:10.1007/s00299-005-0015-3
Laine E, Lamblin F, Lacoux J, Dupre P, Roger D, Sihachakr D, David A (2000) Gelling agent influences the detrimental effect of kanamycin on adventitious budding in flax. Plant Cell Tissue Organ Cult 63:77–80
Lee SM, Kang K, Chung H, Yoo SH, Xu XM, Lee SB, Cheong JJ, Daniell H, Kim M (2006) Plastid transformation in the monocotyledonous cereal crop, rice (Oryza sativa) and transmission of transgenes to their progeny. Mol Cells 21:401–410
Li M, Huang ZG, Han LX, Zhao GR, Li YH (2003) Gene transfer strategy for kiwifruit to obtain pure transgenic plant through inducing adventitious roots in leaf explants with Agrobacterium tumefaciens. Proceedings of the fifth international symposium on Kiwifruit, Acta Horticult 610:495–499
Lin JJ, Assad-Garcia N, Kuo J (1995) Plant hormone effect of antibiotics on the transformation efficiency of plant tissues by Agrobacterium tumefaciens cells. Plant Sci 109:171–177
Machado MLD, Machado AD, Hanzer V, Weiss H, Regner F, Steinkellner H, Mattanovich D, Plail R, Knapp E, Kalthoff B, Katinger H (1992) Regeneration of transgenic plants of Prunus armeniaca containing the coat protein gene of plum pox virus. Plant Cell Rep 11:25–29
Maldonado-Perez D, Shah A, Stirling T, Ward D, Riccardi D (2006) The attenuation of aminoglycoside-induced renal callular toxicity by lithium and by calcium-sensing receptor antagonism. Experimental biology 2006 meeting, FASEB J 20:A341
Masuko T, Kuno T, Kashiwagi K, Kusama T, Williams K, Igarashi K (1999) Stimulatory and inhibitory properties of aminoglycoside antibiotics at N-methyl-d-aspartate receptors. J Pharmacol Exp Ther 290:1026–1033
Mathews H, Wagoner W, Kellogg J, Bestwick RK (1995) Genetic transformation of strawberry: stable integration of a gene to control biosynthesis of ethylene. In Vitro Cell Dev Biol Plant 31:36–43
Mathias RJ, Boyd LA (1986) Cefotaxime stimulates callus growth, embryogenesis and regeneration in hexaploid bread wheat (Triticum aestivum L. em Thell). Plant Sci 46:217–223
Mathias RJ, Mukasa C (1987) The effect of cefotaxime on the growth and regeneration of callus from 4 varieties of barley (Hordeum vulgare L.). Plant Cell Rep 6:454–457
McCabe MS, Klaas M, Gonzalez-Rabade N, Poage M, Badillo-Corona JA, Zhou F, Karcher D, Bock R, Gray JC, Dix PJ (2008) Plastid transformation of high-biomass tobacco variety ‘Maryland Mammoth’ for production of human immunodeficiency virus type 1 (HIV-1) p24 antigen. Plant Biotechnol J 6:914–929. doi:10.1111/j.1467-7652.2008.00365.x
Mead FC, Williams AJ (2004) Electrostatic mechanisms underlie neomycin block of the cardiac ryanodine receptor channel (RyR2). Biophys J 87:3814–3825. doi:10.1529/biophysj.104.049338
Mentewab A, Stewart CN (2005) Overexpression of an Arabidopsis thaliana ABC transporter confers kanamycin resistance to transgenic plants. Nat Biotechnol 23:1177–1180. doi:10.1038/nbt1134
Miguel CM, Oliveira MM (1992) Transgenic almond (Prunus dulcis Mill.) plants obtained by Agrobacterium-mediated transformation of leaf explants. Plant Cell Rep 18:387–393
Mihaljevic S, Peric M, Jelaska S (2001) The sensitivity of embryogenic tissue of Picea omorika (Panc.) Purk. to antibiotics. Plant Cell Tissue Organ Cult 67:287–293
Miki B, McHugh S (2004) Selectable marker genes in transgenic plants: applications, alternatives and biosafety. J Biotechnol 107:193–232. doi:10.1016/j.jbiotec.2003.10.011
Mingeot-Leclercq MP, Tulkens PM (1999) Aminoglycosides: nephrotoxicity. Antimicrob Agents Chemother 43:1003–1012
Moazed D, Noller HF (1987) Interaction of antibiotics with functional sites in 16S ribosomal RNA. Nature 327:389–394
Morris JC, Mensa-Wilmot K (1997) Role of 2, 6-dideoxy-2, 6-diaminoglucose in activation of a eukaryotic phospholipase C by aminoglycoside antibiotics. J Biol Chem 272:29554–29559
Noller HF (1991) Ribosomal-RNA and translation. Annu Rev Biochem 60:191–227
Nomura K, Naruse K, Watanabe K, Sokabe M (1990) Aminoglycoside blockade of Ca2+-activated K+ channel from rat-brain synaptosomal membranes incorporated into planar bilayers. J Membr Biol 115:241–251
Notenboom S, Wouterse AC, Peters B, Kuik LH, Heemskerk S, Russel FGM, Masereeuw R (2006) Increased apical insertion of the multidrug resistance protein 2 (MRP2/ABCC2) in renal proximal tubules following gentamicin exposure. J Pharmacol Exp Ther 318:1194–1202. doi:10.1124/jpet.106.104547
Oreifig AS, Kovacs G, Jenes B, Kiss E, Scott P, Toldi O (2004) Development of a non-lethal selection system by using the aadA marker gene for efficient recovery of transgenic rice (Oryza sativa L.). Plant Cell Rep 22:490–496. doi:10.1007/s00299-003-0715-5
Owens LD (1979) Kanamycin promotes morphogenesis of plant tissues. Plant Sci Lett 16:225–230
Ozaki S, DeWald DB, Shope JC, Chen J, Prestwich GD (2000) Intracellular delivery of phosphoinositides and inositol phosphates using polyamine carriers. Proc Natl Acad Sci USA 97:11286–11291
Padilla IMG, Webb K, Scorza R (2003) Early antibiotic selection and efficient rooting and acclimatization improve the production of transgenic plum plants (Prunus domestica L.). Plant Cell Rep 22:38–45. doi:10.1007/s00299-003-0648-z
Parsons TD, Obaid AL, Salzberg BM (1992) Aminoglycoside antibiotics block voltage-dependent calcium channels in intact vertebrate nerve terminals. J Gen Physiol 99:491–504
Perez-Barranco G, Torreblanca R, Padilla IMG, Sanchez-Romero C, Pliego-Alfaro F, Mercado JA (2009) Studies on genetic transformation of olive (Olea europaea L.) somatic embryos: I. Evaluation of different aminoglycoside antibiotics for nptII selection; II. Transient transformation via particle bombardment. Plant Cell Tissue Organ Cult 97:243–251. doi:10.1007/s11240-009-9520-3
Perl A, Galili S, Shaul O, Bentzvi I, Galili G (1993) Bacterial dihydrodipicolinate synthase and desensitized aspartate kinase-2 novel selectable markers for plant transformation. Bio-Technology 11:715–718
Petri C, Burgos L (2005) Transformation of fruit trees. Useful breeding tool or continued future prospect? Transgenic Res 14:15–26. doi:10.1007/s11248-004-2770-2
Petri C, Alburquerque N, Burgos L (2005) The effect of aminoglycoside antibiotics on the adventitious regeneration from apricot leaves and selection of nptII-transformed leaf tissues. Plant Cell Tissue Organ Cult 80:271–276
Pichler M, Wang ZY, GrabnerWeiss C, Reimer D, Hering S, Grabner M, Glossmann H, Striessnig J (1996) Block of P/Q-type calcium channels by therapeutic concentrations of aminoglycoside antibiotics. Biochemistry 35:14659–14664
Polowick PL, Quandt J, Mahon JD (2000) The ability of pea transformation technology to transfer genes into peas adapted to western Canadian growing conditions. Plant Sci 153:161–170
Raisinghani M, Premkumar LS (2005) Block of native and cloned vanilloid receptor 1 (TRPV1) by aminoglycoside antibiotics. Pain 113:123–133. doi:10.1016/j.pain.2004.09.042
Rakosy-Tican E, Aurori CM, Dijkstra C, Thieme R, Aurori A, Davey MR (2007) The usefulness of the gfp reporter gene for monitoring Agrobacterium-mediated transformation of potato dihaploid and tetraploid genotypes. Plant Cell Rep 26:661–671. doi:10.1007/s00299-006-0273-8
Ramesh SA, Kaiser BN, Franks T, Collins G, Sedgley M (2006) Improved methods in Agrobacterium-mediated transformation of almond using positive (mannose/pmi) or negative (kanamycin resistance) selection-based protocols. Plant Cell Rep 25:821–828. doi:10.1007/s00299-006-0139-0
Ranjan A, Pothayee N, Seleem MN, Tyler RD Jr, Brenseke B, Sriranganathan N, Riffle J, Kasimanickam R (2009) Antibacterial efficacy of core-shell nanostructures encapsulating gentamicin against an in vivo intracellular Salmonella model. Int J Nanomed 4:289–297
Rohini VK, Rao KS (2000) Transformation of peanut (Arachis hypogaea L.): a non-tissue culture based approach for generating transgenic plants. Plant Sci 150:41–49
Rosellini D, LaFayette PR, Barone P, Veronesi F, Parrott WA (2004) Kanamycin-resistant alfalfa has a point mutation in the 16S plastid rRNA. Plant Cell Rep 22:774–779. doi:10.1007/s00299-004-0757-3
Rosellini D, Capomaccio S, Ferradini N, Sardaro MLS, Nicolia A, Veronesi F (2007) Non-antibiotic, efficient selection for alfalfa genetic engineering. Plant Cell Rep 26:1035–1044. doi:10.1007/s00299-007-0321-z
Saha B, Bhattacharya J, Mukherjee A, Ghosh AK, Santra CR, Dasgupta AK, Karmakar P (2007) In vitro structural and functional evaluation of gold nanoparticles conjugated antibiotics. Nanoscale Res Lett 2:614–622
Schmitt F, Oakeley EJ, Jost JP (1997) Antibiotics induce genome-wide hypermethylation in cultured Nicotiana tabacum plants. J Biol Chem 272:1534–1540
Schmϋlling T, Schell J (1993) Transgenic tobacco plants regenerated from leaf disks can be periclinal chimeras. Plant Mol Biol 21:705–708
Scholz-Starke J, Carpaneto A, Gambale F (2006) On the interaction of neomycin with the slow vacuolar channel of Arabidopsis thaliana. J Gen Physiol 127:329–340. doi:10.1085/jpg.200509402
Scott A, Woodfield D, White DWR (1998) Allelic composition and genetic background effects on transgene expression and inheritance in white clover. Mol Breed 4:479–490
Shi LJ, Liu LA, Cheng XH, Wang CA (2002) Decrease in acetylcholine-induced current by neomycin in PC12 cells. Arch Biochem Biophys 403:35–40
Silhavy D, Maliga P (1998) Plastid promoter utilization in a rice embryogenic cell culture. Curr Genet 34:67–70
Spahn CMT, Prescott CD (1996) Throwing a spanner in the works: antibiotics and the translation apparatus. J Mol Med 74:423–439
Stacey DJ, McLean WG (2000) Cytoskeletal protein mRNA expression in the chick utricle after treatment in vitro with aminoglycoside antibiotics: effects of insulin, iron chelators and cyclic nucleotides. Brain Res 871:319–332
Teixeira da Silva JA, Fukai S (2003) Effect of aminoglycoside antibiotics on in vitro morphogenesis from cultured cells of chrysanthemum and tobacco. J Plant Biol 46:71–82
Tiboni O, Chinali G (1997) Inhibition of chloroplast protein synthesis by kirromycin: action of the antibiotic on elongation factor Tu. Plant Physiol Biochem 35:23–29
Todd JH, Sens DA, Hazenmartin DJ, Bylander JE, Smyth BJ, Sens MA (1992) Aminoglycoside antibiotics alter the electrogenic transport properties of cultured human proximal tubule cells. Toxicol Pathol 20:608–616
Walter F, Vicens Q, Westhof E (1999) Aminoglycoside–RNA interactions. Curr Opin Chem Biol 3:694–704
Weeks JT, Koshiyama KY, Maier-Greiner U, Schaeffner T, Anderson OD (2000) Wheat transformation using cyanamide as a new selective agent. Crop Sci 40:1749–1754
Weide R, Koornneef M, Zabel P (1989) A simple, nondestructive spraying assay for the detection of an active kanamycin resistance gene in transgenic tomato plants. Theor Appl Genet 78:169–172
Wilhem JM, Pettitt SE, Jessop JJ (1978) Aminoglycoside antibiotics and eukaryotic protein synthesis: Structure–function relationships in stimulation of misreading with a wheat embryo system. Biochemistry 17:1143–1149
Winegar BD, Haws CM, Lansman JB (1996) Subconductance block of single mechanosensitive ion channels in skeletal muscle fibers by aminoglycoside antibiotics. J Gen Physiol 107:433–443
Wright GD, Berghuis AM, Mobashery S (1998) Aminoglycoside antibiotics—structures, functions, and resistance. In: Rosen BP, Mobashery S (eds) Resolving the antibiotic paradox. Kluwer Academic and Plenum Publishers, New York, pp 27–69
Yao JL, Cohen D, Atkinson R, Richardson K, Morris B (1995) Regeneration of transgenic plants from the commercial apple cultivar ‘Royal Gala’. Plant Cell Rep 14:407–412
Yaronskaya EB, Gritskevich ER, Trukhanovets NL, Averina NG (2007) Effect of kinetin on early stages of chlorophyll biosynthesis in streptomycin-treated barley seedlings. Russ J Plant Physiol 54:388–395. doi:10.1134/S1021443707030144
Yeh KC, To KY, Sun SW, Wu MC, Lin TY, Chen CC (1994) Point mutations in the chloroplast 16S ribosomal-RNA gene confer streptomycin resistance in Nicotiana plumbaginifolia. Curr Genet 26:132–135
Yeiser AJ, Cox JR, Wright SN (2004) Voltage-dependent inhibition of rat skeletal muscle sodium channels by aminoglycoside antibiotics. Pflugers Archiv Eur J Physiol 448:204–213. doi:10.1007/s00424-004-1244-y
Yepes LM, Aldwinckle HS (1994) Factors that affect leaf regeneration efficiency in apple, and effect of antibiotics in morphogenesis. Plant Cell Tissue Organ Cult 37:257–269
Youssef SS, Moghaieb REA, Saker MM, El Awady M, El Sharkawy A (2007) Transformation of faba bean (Vicia faba L.): a non-tissue culture based approach for generating transgenic plants. In Vitro Cell Dev Biol Animal 43: S28
Zhang BH, Liu F, Liu ZH, Wang HM, Yao CB (2001) Effects of kanamycin on tissue culture and somatic embryogenesis in cotton. Plant Growth Regul 33:137–149
Zilkah S, Gressel J (1977) Cell-cultures vs whole plants for measuring phytotoxicity. 3. Correlations between phyto-toxicities in cell-suspension cultures, calli and seedlings. Plant Cell Physiol 18:815–820
Zilkah S, Bocion PF, Gressel J (1977) Cell cultures vs whole plants for measuring phytotoxicity.2. Correlations between phytotoxicity in seedlings and calli. Plant Cell Physiol 18:657–670
Acknowledgments
This work was partially supported by BIOCARM BIO-AGR07/04-0011 and Séneca 08665/PI/08. IMGP thanks the Spanish Council of Scientific Research (CSIC) for a I3P post-doctoral contract. The authors thank Prof. Fernando Pliego-Alfaro for the critical review of the manuscript and Dr. David J. Walker for English language editing.
Author information
Authors and Affiliations
Corresponding author
Additional information
Communicated by R. Reski.
Rights and permissions
About this article
Cite this article
Padilla, I.M.G., Burgos, L. Aminoglycoside antibiotics: structure, functions and effects on in vitro plant culture and genetic transformation protocols. Plant Cell Rep 29, 1203–1213 (2010). https://doi.org/10.1007/s00299-010-0900-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00299-010-0900-2