Plant growth-promoting bacteria can affect plant growth and development in two different ways: indirectly or directly (Glick 1995; Glick et al. 1999). Indirect promotion of plant growth occurs when these bacteria decrease or prevent some of the deleterious effects of a phytopathogenic organism by any one or more of several different mechanisms. In general, bacteria can directly promote plant growth by providing the plant with a compound that is synthesized by the bacterium or facilitating the uptake of nutrients.
There are several ways in which plant growth-promoting bacteria can directly facilitate the proliferation of their plant hosts. They may fix atmospheric nitrogen; produce siderophores which can solubilize and sequester iron and provide it to plants; synthesize phytohormones, including auxins, cytokinins, and gibberellins which can enhance various stages of plant growth; solubilize minerals such as phosphorus; and synthesize enzymes that can modulate plant growth and development (Brown 1974; Kloepper et al. 1986, 1989; Davison 1988; Lambert and Joos 1989; Patten and Glick 1996; Glick et al. 1999). A particular bacterium may affect plant growth and development using any one, or more, of these mechanisms.Moreover, many plant growthpromoting bacteria possess several properties that enable them to facilitate plant growth and, of these, may utilize different ones at various times during the life cycle of the plant.
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References and Selected Reading
Abeles FB (1973) Ethylene in plant biology. Academic Press, New York, 302 pp
Abeles FB, Morgan PW, Saltveit ME Jr (1992) Ethylene in plant biology, 2nd edn. Acade-mic Press, San Diego
Bashan Y (1994) Symptom expression and ethylene production in leaf blight of cotton caused by Alternaria macrospora and Alternaria alternata alone and combined. Can J Bot 72:1574-1579
Belimov AI, Safronova, VI, Sergeyeva TA, Egorova TN, Matveyeva VA, Tsyganov VE, Borisov AY, Tikhonovich IA, Kluge C, Preisfeld A, Dietz K-J, Stepanok VV (2001) Char-acterization of plant growth promoting rhizobacteria isolated from polluted soils and containing 1-aminocyclopropane-1-carboxylate deaminase. Can J Microbiol 27:642-652
Bestwick RK, Ferro AJ (1998) Reduced ethylene synthesis and delayed fruit ripening in transgenic tomatoes expressing S-adenosylmethionine hydrolase. US Patent No: 5, 723, 746
Biles CL, Abeles FB, Wilson CL (1990) The role of ethylene in anthracnose of cucumber, Cucumis sativus, caused by Colletotrichum lagenarium. Phytopathology 80732-736
Bradford KJ, Yang SF (1980) Xylem transport of 1-aminocyclopropane-1-carboxylic acid, an ethylene precursor, in waterlogged tomato plants. Plant Physiol 65:322-326
Brown ME (1974) Seed and root bacterization. Annu Rev Phytopathol 12:181-197
Burd GI, Dixon DG, Glick BR (1998) A plant growth-promoting bacterium that decreases nickel toxicity in seedlings. Appl Environ Microbiol 64:3663-3668
Campbell BG, Thomson JA (1996) 1-Aminocyclopropane-1-carboxylate deaminase genes from Pseudomonas strains. FEMS Microbiol Lett 138:207-210
Cohen R, Riov J, Lisker N, Katan J (1986) Involvement of ethylene in herbicide-induced resistance to Fusarium oxysporum f. sp. melonis. Phytopathology 76:1281-1285
Cronshaw DK, Pegg GF (1976) Ethylene as a toxin synergist in Verticillium wilt of tomato. Physiol Plant Pathol 9:33-38
Davison J (1988) Plant beneficial bacteria. Bio/Technology 6:282-286
Elad Y (1988) Involvement of ethylene in the disease caused by Botrytis cinerea on rose and carnation flowers and the possibility of control. Ann Appl Biol 113:589-598
Elad Y (1990) Production of ethylene in tissues of tomato, pepper, French-bean and cucumber in response to infection by Botrytis cinerea. Physiol Mol Plant Pathol 36:277-287
Else MA, Jackson MB (1998) Transport of 1-aminocyclopropane-1-carboxylic acid (ACC) in the transpiration stream of tomato (Lycopersicon esculentum) in relation to foliar ethylene production and petiole epinasty. Aust J Plant Physiol 25:453-458
Fallik E, Sarig S, Okon Y (1994) Morphology and physiology of plant roots associated with Azospirillum. In: Okon Y (ed) Azospirillum/plant associations. CRC Press, Boca Raton, pp 77-85
Frankenberger WT Jr, Arshad M (1995) Phytohormones in soil. Marcel Dekker, New York
Fukuda H, Ogawa T, Tanase S (1993) Ethylene production by microorganisms. Adv Microb Physiol 35:275-306
Gaudin V, Vrain T, Jouanin L (1994) Bacterial genes modifying hormonal balances in plants. Plant Physiol Biochem 32:11-29
Giovanelli J, Mudd SH, Datko AH (1980) Sulfur amino acids in plants. In: Miflin BJ (ed) Amino acids and derivatives, the biochemistry of plants: a comprehensive treatise. vol 5. Academic Press, New York, pp 453-505
Glick BR (1995) The enhancement of plant growth by free-living bacteria. Can J Micro-biol 41:109-117
Glick BR, Jacobson CB, Schwarze MK, Pasternak JJ (1994) A1-Aminocyclopropane-1-car-boxylic acid deaminase mutants of the plant growth promoting rhizobacterium Pseudomonas putida GR12-2 do not stimulate canola root elongation. Can J Microbiol 40:911-915
Glick BR, Karaturovíc DM, Newell PC (1995) A novel procedure for rapid isolation of plant growth promoting pseudomonads. Can J Microbiol 41:533-536
Glick BR, Penrose DM, Li J (1998) A model for the lowering of plant ethylene concentra-tions by plant growth-promoting bacteria. J Theor Biol 190:63-68
Glick BR, Patten CL, Holguin G, Penrose DM (1999) Biochemical and genetic mecha-nisms used by plant growth-promoting bacteria. Imperial College Press, London
Grichko VP, Glick BR (2000) Identification of DNA sequences that regulate the expres-sion of the Enterobacter cloacae UW4 1-aminocyclopropane-1-carboxylate deami-nase gene. Can J Microbiol 46:1159-1165
Grichko VP, Glick BR (2001) Amelioration of flooding stress by ACC deaminase-con-taining plant growth-promoting bacteria. Plant Physiol Biochem 39:11-17
Honma M (1985) Chemically reactive sulfhydryl groups of 1-aminocyclopropane-1-car-boxylate deaminase. Agric Biol Chem 49:567-571
Honma M (1993) Stereospecific reaction of 1-aminocyclopropane-1-carboxylate deami-nase. In: Pech JC, Latché A, Balagué C (eds) Cellular and molecular aspects of the plant hormone ethylene. Kluwer, Dordrecht, pp 111-116
Honma M, Shimomura T (1978) Metabolism of 1-aminocyclopropane-1-carboxylic acid. Agric Biol Chem 42:1825-1831
Hyodo H (1991) Stress/wound ethylene. In: Mattoo AK, Suttle JC (eds) The plant hor-mone ethylene. CRC Press, Boca Raton, pp 65-80
Jacobson CB, Pasternak JJ, Glick BR (1994) Partial purification and characterization of 1-aminocyclopropane-1-carboxylate deaminase from the plant growth promoting rhizobacterium Pseudomonas putida GR12-2. Can J Microbiol 40:1019-1025
Jia Y-J, Kakuta Y, Sugawara M, Igarashi T, Oki N, Kisaki M, Shoji T, Kanetuna Y, Horita T, Matsui H, Honma M (1999) Synthesis and degradation of 1-aminocyclopropane-1-carboxylic acid by Penicillium citrinum. Biosci Biotechnol Biochem 63:542-549
Jia Y-J, Ito H, Matsui H, Honma M (2000) A1-Aminocyclopropane-1-carboxylate (ACC) deaminase induced by ACC synthesized and accumulated in Penicillium citrinum intracellular spaces. Biosci Biotechnol Biochem 64:299-305
John P (1991) How plant molecular biologists revealed a surprising relationship between two enzymes, which took an enzyme out of a membrane where it was not located, and put it into the soluble phase where it could be studied. Plant Mol Biol Rep 9:192-194
Kende H (1989) Enzymes of ethylene biosynthesis. Plant Physiol 91:1-4
Kende H (1993) Ethylene biosynthesis. Annu Rev Plant Physiol Plant Mol Biol 44:283-307
Klee HJ, Kishore GM (1992) Control of fruit ripening and senescence in plants. US Patent No: 5, 702, 933
Klee HJ, Hayford MB, Kretzmer KA, Barry GF, Kishore GM (1991) Control of ethylene synthesis by expression of a bacterial enzyme in transgenic tomato plants. Plant Cell 3:1187-1193
Kloepper JW, Scher FM, Laliberté M, Tipping B (1986) Emergence-promoting rhizobac-teria: description and implications for agriculture. In: Swinburne TR (ed) Iron, siderophores, and plant disease. Plenum, New York, pp 155-164
Kloepper JW, Lifshitz R, Zablotowicz RM (1989) Free-living bacterial inocula for enhancing crop productivity. Trends Biotechnol 7:39-43
Lambert B, Joos H (1989) Fundamental aspects of rhizobacterial plant growth promo-tion research. Trends Biotechnol 7:215-219
Li J, Glick BR (2001) Transcriptional regulation of the Enterobacter cloacae UW4 1-aminocyclopropane-1-carboxylate (ACC) deaminase gene (acdS). Antonie van Leewenhoek 80:255-261
Li J, Ovakim DH, Charles TC, Glick BR (2000) An ACC deaminase minus mutant of Enter-obacter cloacae UW4 no longer promotes root elongation. Curr Microbiol 41:101-105
Lund ST, Stall, RE, Klee HJ (1998) Ethylene regulates the susceptible response to pathogen infection in tomato. Plant Cell 10:371-382
Mattoo AK, Suttle JC (1991) The plant hormone ethylene. CRC Press, Boca Raton
Minami R, Uchiyama K, Murakami T, Kawai J, Mikami K, Yamada T, Yokoi D, Ito H, Mat-sui H, Honma M (1998) Properties, sequence, and synthesis in Escherichia coli of 1-aminocyclopropane-1-carboxylate deaminase from Hansenula saturnus. J Biochem 123:1112-1118
Mizutani F, Golam Rabbany ABM, Akiyoshi H (1998) Inhibition of ethylene production by tropolone compounds in young excised peach pits. J Jpn Soc Hortic Sci 67:166-169
Mol JNM, Holton TA, Koes RE (1995) Floriculture: genetic engineering of commercial traits. Trends Biotechnol 13:350-355
Morgan PW, Drew CD (1997) Ethylene and plant responses to stress. Physiol Plant 100:620-630
Nayani S, Mayak S, Glick BR (1998) The effect of plant growth promoting rhizobacteria on the senescence of flower petals. Ind J Exp Biol 36:836-839
Nie L, Shah S, Rashid A, Burd GI, Dixon GD, Glick BR (2002) Phytoremediation of arsen-ate contaminated soil by transgenic canola and the plant growth-promoting bac-terium Enterobacter cloacae CAL2. Plant Physiol Biochem 40:355-361
Patten CL, Glick BR (1996) Bacterial biosynthesis of indole-3-acetic acid. Can J Microbiol 42:207-220
Penrose DM, Glick BR (2001) Levels of 1-aminocyclopropane-1-carboxylic acid (ACC) in exudates and extracts of canola seeds treated with plant growth-promoting bacte-ria. Can J Microbiol 47:368-372
Penrose DM, Moffatt BM, Glick BR (2001) Determination of 1-aminocyclopropane-1-carboxylic acid (ACC) to assess the effects of ACC deaminase-containing bacteria on roots of canola seedlings. Can J Microbiol 47:77-80
Robinson MM, Shah S, Tamot B, Pauls PK, Moffatt BA, Glick BR (2001) Reduced symp-toms of Verticillium wilt in tomato plants transformed with ACC deaminase to con-trol ethylene biosynthesis. Mol Plant Pathol 2:135-145
Shah S, Li J, Moffatt BA, Glick BR (1997) ACC deaminase genes from plant growth pro-moting bacteria. In: Ogoshi A, Kobayashi K, Homma Y, Kodama F, Kondo N, Akino S (eds) Plant growth-promoting rhizobacteria: present status and future prospects. OECD, Paris, pp 320-324
Shah S, Li J, Moffatt BA, Glick BR (1998) Isolation and characterization of ACC deami-nase genes from two different plant growth promoting rhizobacteria. Can J Microbiol 44:833-843
Sheehy RE, Honma M, Yamada M, Sasaki T, Martineau B, Hiatt WR (1991) Isolation, sequence, and expression in Escherichia coli of the Pseudomonas sp. strain ACP gene encoding 1-aminocyclopropane-1-carboxylate deaminase. J Bacteriol 173:5260-5265
Shiu OY, Oetiker JH, Yip WK, Yang SF (1998) The promoter of LE-ACS7, an early flood-ing-induced 1-aminocyclopropane carboxylate synthase gene of the tomato, is tagged by a Sol3 transposon. Proc Natl Acad Sci USA 95:10334-10339
Sisler EC, Serek M (1997) Inhibitors of ethylene responses in plants at the receptor level: recent developments. Physiol Plant 100:577-582
Tien TM, Gaskins MH, Hubell DH (1979) Plant growth substances produced by Azospir-illum brasilense and their effect on the growth of pearl millet (Pennisetum ameri-canum L). Appl Environ Microbiol 37:1016-1024
Van Loon LC (1984) Regulation of pathogenesis and symptom expression in diseased plants by ethylene. In: Fuchs Y, Chalutz E (eds) Ethylene: biochemical, physiological and applied aspects. Martinus Nijhoff/Dr. W. Junk, The Hague, pp 171-180
Wang C, Knill E, Glick BR, Défago G (2000) Effect of transferring 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase genes into Pseudomonas fluorescens strain CHA0 and its gacA derivative CHA96 on their growth-promoting and disease-suppressive capacities. Can J Microbiol 46:898-907
Whipps JM (1990) Carbon utilization. In: Lynch JM (ed) The rhizosphere. Wiley Inter-science, Chichester, pp 59-97
Woltering EJ, Van Doorn WG (1988) Role of ethylene in senescence of petals - morpho-logical and taxonomical relationships. J Exp Bot 39:1605-1616
Yang SF, Hoffman NE (1984) Ethylene biosynthesis and its regulation in higher plants. Annu Rev Plant Physiol 35:155-189
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Glick, B.R., Penrose, D.M. (2008). The Use of ACC Deaminase-Containing Plant Growth-Promoting Bacteria to Protect Plants Against the Deleterious Effects of Ethylene. In: Varma, A., Abbott, L., Werner, D., Hampp, R. (eds) Plant Surface Microbiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-74051-3_8
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