Abstract
The interactions between the plant and endophytic bacteria in the shoots likely differ to some extent from those in the roots. Shoot endophytic bacteria are typically isolated during plant tissue culture started from shoot tips (buds) or embryos. With methods such as in situ hybridization and transmission electron microscopy, endophytic bacteria have been localized in buds, seeds, and flowers of forest trees, and GFP tagging has been used to observe colonization of seedlings by endophytic bacteria. Vertical transmission of endophytic bacteria has been suggested. Shoot endophytic bacteria share many plant growth-promoting effects with the root endophytes, the ability of producing plant growth hormones and nitrogen fixation being the most common ones. In addition, some shoot endophytes may affect plant growth through production of adenine derivatives and vitamin B12. Many more likely remain to be determined by powerful methods such as genomics and metabolomics, which will be valuable tools for describing the significance of endophytic bacteria for forest trees in the future.
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Abbreviations
- (TEM):
-
transmission electron microscopy
- (PHB):
-
polyhydroxybutyrate
- (GFP):
-
green fluorescent protein
- (IAA):
-
Indole-acetic acid
References
Akiyoshi DE, Regier DA, Gordon MP (1987) Cytokinin production by Agrobacterium and Pseudomonas spp. J Bacteriol 169:4242–4248
Baldani JI, Caruso L, Baldani VLD et al (1997) Recent advances in BNF with non legume plants. Soil Biol Biochem 29:911–922
Bandara WMMS, Seneviratne G, Kulasooriya SA (2006) Interactions among endophytic bacteria and fungi: effects and potentials. J Biosci 31:645–650
Basile DV, Basile MR, Li QY et al (1985) Vitamin B12-stimulated growth and development of Jungermannia leiantha Grolle and Gymnocolea inflata (Huds.) Dum. (Hepaticae). Bryologist 88:77–81
Bastián F, Cohen A, Piccoli P et al (1998) Production of indole-3-acetic acid and gibberellins A1 and A3 by Acetobacter diazotrophicus and Herbaspirillum seropedicae in chemically-defined cultures. Plant Growth Regul 24:7–11
Baumann TW, Schulthess BH, Linden A et al (1994) Structure and metabolism of t-β-D-glucopyranosyladenine. The product of a cytokinin-sparing reaction? Phytochemistry 36: 537–542
Bottini R, Cassán F, Piccoli P (2004) Gibberellin production by bacteria and its involvement in plant growth promotion and yield increase. Appl Microbiol Biotechnol 65:497–503
Brandl MT, Lindow SE (1996) Cloning and characterization of a locus encoding an indolepyruvate decarboxylase involved in indole-3-acetic acid synthesis in Erwinia herbicola. Appl Environ Microbiol 62:4121–4128
Cankar K, Kraigher H, Ravnikar M et al (2005) Bacterial endophytes from seed of Norway spruce (Picea abies L. Karst). FEMS Microbiol Lett 244:341–345
Costacurta A, Mazzafera P, Rosato Y (1998) Indole-3-acetic acid biosynthesis by Xanthomonas axonopodis pv. citri is increased in the presence of plant leaf extracts. FEMS Microbiol Lett 159:215–220
Dalla Santa OR, Hernández RF, Alvarez GLM et al (2004) Azospirillum sp. inoculation in wheat, barley and oats seeds greenhouse experiments. Braz Arch Biol Technol 47:843–850
DeLong EF, Wickham GS, Pace NR (1989) Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells. Science 243:1360–1363
Doronina NV, Ivanova EG, Trotsenko YA (2002) New evidence for the ability of methylobacteria and methanotrophs to synthesize auxins. Mikrobiologiya 71:130–132
Doronina NV, Ivanova EG, Suzina NE et al (2004) Methanotrophs and methylobacteria are found in woody plant tissues within the winter period. Mikrobiologiya 73:702–709
Doty SL, Oakley B, Xin G et al (2009) Diazotrophic endophytes of native black cottonwood and willow. Symbiosis 47:23–33
Fall R (1996) Cycling of methanol between plants, methylotrophs and the atmosphere. In: Lidstrom ME, Tabita FR (eds) Microbial growth on C1 compounds. Kluwer, Dordrecht, pp 343–350
Fall R, Benson AA (1996) Leaf methanol – the simplest natural product from plants. Trends Plant Sci 1:296–301
Ferreira A, Quecine MC, Lacava PT et al (2008) Diversity of endophytic bacteria from Eucalyptus species seed and colonization of seedlings by Pantoea agglomerans. FEMS Microbiol Lett 287:8–14
Freyermuth SK, Long RLG, Mathur S et al (1996) Metabolic aspects of plant interaction with commensal methylotrophs. In: Lidstrom ME, Tabita RF (eds) Microbial growth on C1 compounds. Kluwer, Dordrecht, pp 277–284
Gamalero E, Fracchia L, Cavaletto M et al (2003) Characterization of functional traits of two fluorescent pseudomonads isolated from basidiomes of ectomycorrhizal fungi. Soil Biol Biochem 35:55–65
Garcia de Salamone IE, Hynes RK, Nelson LM (2001) Cytokinin production by plant growth promoting rhizobacteria and selected mutants. Can J Microbiol 47:404–411
George EF, Sherrington PD (1984) Plant propagation by tissue culture methods. Handbook and directory of commercial laboratories. Eastern Press, Reading
Holland MA (1997) Occam’s razor applied to hormonology. Are cytokinins produced by plants? Plant Physiol 115:865–868
Holland MA, Polacco JC (1992) Urease-null and hydrogenase-null phenotypes of a phylloplane bacterium reveal altered nickel metabolism in two soybean mutants. Plant Physiol 98:942–948
Holland MA, Polacco JC (1994) PPFMs and other covert contamination: is there more to plant physiology than just plant? Annu Rev Plant Phys Plant Mol Biol 45:197–209
Ivanova EG, Doronina NV, Shepelyakovskaya AO et al (2000) Facultative and obligate aerobic methylobacteria synthesize cytokinins. Mikrobiologiya 69:764–769
Ivanova EG, Doronina NV, Trotsenko YA (2001) Aerobic methylobacteria are capable of synthesizing auxins. Microbiologiya 70:452–458
Ivanova EG, Fedorov DN, Doronina NV et al (2006) Production of vitamin B12 in aerobic methylotrophic bacteria. Microbiologiya 75:494–496
Ivanova EG, Pirttilä AM, Fedorov DNF et al (2008) Association of methylotrophic bacteria with plants: metabolic aspects. In: Sorvari S, Pirttilä AM (eds) Prospects and applications for plant associated microbes. A laboratory manual, part A: bacteria. Biobien Innovations, Turku, pp 225–231
Kalyaeva MA, Zakharchenko NS, Doronina NV et al (2001) Plant growth and morphogenesis in vitro is promoted by associative methylotrophic bacteria. Russ J Plant Physiol 48:514–517
Kamoun R, Lepoivre P, Boxus P (1998) Evidence for the occurrence of endophytic prokaryotic contaminants in micropropagated plantlets of Prunus cerasus cv. ‘Montgomery’. Plant Cell Tissue Org Cult 52:57–59
Keppler F, Hamilton JTG, Bra M et al (2006) Methane emissions from terrestrial plants under aerobic conditions. Nature 439:187–191
Koenig RL, Morris RO, Polacco JC (2002) tRNA is the source of low-level trans-zeatin production in Methylobacterium spp. J Bacteriol 184:1832–1842
Koopman V, Kutschera U (2005) In vitro regeneration of sunflower plants: effects of a Methylobacterium strain on organ development. J Appl Bot Food Qual 79:59–62
Koskimäki JJ, Nylund S, Suorsa M et al (2010) Mycobacterial endophytes are enriched during micropropagation of Pogonatherum paniceum. Env Microbiol Rep 2:619–624
Koutsompogeras P, Kyriacou A, Zabetakis I (2007) The formation of 2,5-dimethyl-4-hydroxy-2 H-furan-3-one by cell free extracts of Methylobacterium extorquens and strawberry (Fragaria × ananassa cv. Elsanta). Food Chem 104:1654–1661
Lata H, Li XC, Silva B et al (2006) Identification of IAA-producing endophytic bacteria from micropropagated Echinacea plants using 16 S rRNA sequencing. Plant Cell Tiss Org Cult 85:353–359
Laukkanen H, Soini H, Kontunen-Soppela S et al (2000) A mycobacterium isolated from tissue cultures of mature Pinus sylvestris interferes with growth of Scots pine seedlings. Tree Physiol 20:915–920
Long HH, Schmidt DD, Baldwin IT (2008) Native bacterial endophytes promote host growth in a species-specific manner; phytohormone manipulations do not result in common growth responses. PLoS ONE 3:e2702
Madmony A, Chernin L, Pleban S et al (2005) Enterobacter cloacae, an obligatory endophyte of pollen grains of Mediterranean pines. Folia Microbiol 50:209–216
Merzaeva OV, Shirokikh IG (2010) The production of auxins by the endophytic bacteria of winter rye. Appl Biochem Microbiol 46:51–57
Moore FP, Barac T, Borremans B et al (2006) Endophytic bacterial diversity in poplar trees growing on a BTEX-contaminated site: the characterisation of isolates with potential to enhance phytoremediation. Syst Appl Microbiol 29:539–556
Moritz T, Sundberg B (1996) Endogenous cytokinins in the vascular cambial region of Pinus sylvestris during activity and dormancy. Physiol Plant 98:693–698
Murthy BNS, Vettakkorumakankav NN, KrishnaRaj S et al (1999) Characterization of somatic embryogenesis in Pelargonium × hortorum mediated by a bacterium. Plant Cell Rep 18: 607–613
Nishio N, Tanaka M, Matsuno R et al (1977) Production of vitamin B12 by methanol-utilizing bacteria, Pseudomonas AM-1 and Microcyclus eburneus. Ferment Technol 55:200–203
Nonomura AM, Benson AA (1991) The path of carbon in photosynthesis: improved crop yields with methanol. PNAS 89:9794–9798
Pirttilä AM (2010) Colonization of tree shoots by endophytic fungi. In: Pirttilä AM, Sorvari S (eds) Prospects and applications for plant-associated microbes. A laboratory manual, part B: fungi. BioBien Innovations, Turku
Pirttilä AM, Laukkanen H, Pospiech H et al (2000) Detection of intracellular bacteria in the buds of Scotch pine (Pinus sylvestris L.) by in situ hybridization. Appl Environ Microbiol 66: 3073–3077
Pirttilä AM, Laukkanen H, Hohtola A (2002) Chitinase production in pine callus (Pinus sylvestris L.): a defense reaction against endophytes? Planta 214:848–852
Pirttilä AM, Pospiech H, Laukkanen H et al (2003) Two endophytic fungi in different tissues of Scots pine buds (Pinus sylvestris L.). Microb Ecol 45:53–62
Pirttilä AM, Joensuu P, Pospiech H et al (2004) Bud endophytes of Scots pine produce adenine derivatives and other compounds that affect morphology and mitigate browning of callus cultures. Physiol Plant 121:305–312
Pirttilä AM, Pospiech H, Laukkanen H et al (2005) Seasonal variation in location and population structure of endophytes in buds of Scots pine. Tree Physiol 25:289–297
Pirttilä AM, Hohtola A, Ivanova EG et al (2008) Identification and localization of methylotrophic plant-associated bacteria. In: Sorvari S, Pirttilä AM (eds) Prospects and applications for plant associated microbes. A laboratory manual, part A: bacteria. Biobien Innovations, Turku, pp 218–224
Podolich O, Laschevskyy V, Ovcharenko L et al (2009) Methylobacterium sp. resides in unculturable state in potato tissues in vitro and becomes culturable after induction by Pseudomonas fluorescens IMGB163. J Appl Microbiol 106:728–737
Reed BM, Mentzer J, Tanprasert P et al (1998) Internal bacterial contamination of micropropagated hazelnut: identification and antibiotic treatment. Plant Cell Tiss Org Cult 52:67–70
Scherling C, Ulrich K, Ewald D et al (2009) Metabolic signature of the beneficial interactionof the endophyte Paenibacillus sp. isolate and in vitro–grown poplar plants revealed by metabolomics. Mol Plant Microbe Interact 22:1032–1037
Skoog F, Armstrong DJ (1970) Cytokinins. Annu Rev Plant Physiol 21:359–384
Taghavi A, Garafola C, Monchy S et al (2009) Genome survey and characterization of endophytic bacteria exhibiting a beneficial effect on growth and development of poplar trees. Appl Environ Microbiol 75:748–757
Tanaka S, Walter KS, Schnoor JL (2008) Methods to investigate the role of endophytes in phytoremediation. In: Sorvari S, Pirttilä AM (eds) Prospects and applications for plant associated microbes. A laboratory manual, part A: bacteria. Biobien Innovations, Turku, pp 325–332
Timmusk S, Nicander B, Granhall U et al (1999) Cytokinin production by Paenibacillus polymyxa. Soil Biol Biochem 31:1847–1852
Ulrich K, Ulrich A, Ewald D (2008) Paenibacillus- a predominant endophytic bacterium colonizing tissue cultures of woody plants. Plant Cell Tiss Organ Cult 93:347–351
Van Aken B, Peres CM, Doty SL et al (2004) Methylobacterium populi sp. nov., a novel aerobic, pink-pigmented, facultatively methylotrophic, methane-utilizing bacterium isolated from poplar trees (Populus deltoides x nigra DN34). Int J Syst Evol Microbiol 54:1191–1196
Visser C, Murthy BNS, Odumeru J et al (1994) Modulation of somatic embryogenesis in hypocotyl cultures of geranium (Pelargonium × hortorum Bailey) cv. Ringo Rose by a bacterium. In Vitro Cell Dev Biol 30P:140–143
Yrjälä K, Mancano G, Fortelius C et al (2010) The incidence of Burkholderia in epiphytic and endophytic bacterial cenoses in hybrid aspen grown on sandy peat. Boreal Environ Res15:81–96
Zabetakis I (1997) Enhancement of flavour biosynthesis from strawberry (Fragaria × ananassa) callus cultures by Methylobacterium species. Plant Cell Tiss Org Cult 50:179–183
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This work was supported by the Academy of Finland (Projects no. 129852, 113607).
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Pirttilä, A.M. (2011). Endophytic Bacteria in Tree Shoot Tissues and Their Effects on Host. In: Pirttilä, A., Frank, A. (eds) Endophytes of Forest Trees. Forestry Sciences, vol 80. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-1599-8_8
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