Skip to main content
Log in

Growth and photosynthetic efficiency promotion of sugar beet (Beta vulgaris L.) by endophytic bacteria

  • Regular Paper
  • Published:
Photosynthesis Research Aims and scope Submit manuscript

Abstract

Very little is known about the physiological interactions between plants and endophytic bacteria. We investigated the impact of three endophytic bacteria, Bacillus pumilus 2-1, Chryseobacterium indologene 2-2, and Acinetobacter johnsonii 3-1, on the photosynthetic capacity and growth of sugar beet. Endophyte-free plants were obtained first and infected with the bacteria. Measurements of total chlorophyll content revealed very significant differences between endophyte-free beet plants and some infected by endophytic bacteria. The maximum photochemical yield (Fv/Fm) was used to determine any photosynthetic effect on plants caused by biotic or abiotic factors. After 30 days of growth, there was significantly higher Fv/Fm for endophyte-infected than endophyte-free plants. The light response curves of beet showed that photosynthetic capacity was significantly increased in endophyte-infected plants. Photosynthesis of endophyte-free plants was saturated at 1,300 μmol m−2 s−1, whereas endophyte-infected plants were not saturated at the irradiance used. The effect seemed to be due to promotion of electron transport in the thylakoid membranes. Promotion of photosynthetic capacity in sugar beet was due to increased chlorophyll content, leading to a consequent increased carbohydrate synthesis. It is possible that the increased maximum yield of photosynthesis in sugar beet was promoted by phytohormones and produced by the bacteria.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Arteca RN (1996) Plant growth substances: principles and applications. Chapman and Hall Press, New York, USA, p 332

    Google Scholar 

  • Bacon CW (1993) Abiotic stress tolerances (moisture, nutrients) and photosynthesis in endophytic-infected tall fescue. Agric Ecosyst Environ 44:123–141

    Article  Google Scholar 

  • Bacon CW, Hinton DM (1996) Isolation and culture of endophytic bacteria and fungi. In: Hurst CJ, Knudsen GR, McInerney MJ, Stetzenbach C, Walter MV (eds) Manual of environmental microbiology. ASM Press, Washington, DC, USA, pp 413–421

    Google Scholar 

  • Belesky DP, Devine OJ, Pallas JE Jr, Stringer WE (1987) Photosynthetic activity of tall fescue as influenced by a fungal endophyte. Photosynthetica 21:82–87

    Google Scholar 

  • Bjorkman O, Demmig B (1987) Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins. Planta 170:489–504

    Article  Google Scholar 

  • Cheplick GP, Clay K, Marks S (1989) Interactions between infection by endophytic fungi and nutrient limitation in the grasses Lolium perenne and Festuca arundinacea. New Phytol 111:89–97

    Article  Google Scholar 

  • Clay K (1987) Effects of fungal endophytes on the seed and seedling biology of Lolium perene and Festuca arundinacea. Oecologia 73:358–362

    Article  Google Scholar 

  • Clay K (1990) Fungal endophytes of grasses. Annu Rev Ecol Syst 21:275–297

    Article  Google Scholar 

  • Dietz KJ, Huber U (1984) Rate limiting factors in leaf photosynthesis. I. Carbon fluxes in the Calvin cycle. Biochim Biophys Acta 767:432–443

    Article  CAS  Google Scholar 

  • Dietz KJ, Huber U (1986) Light and CO2 limitation of photosynthesis and states of the reactions regenerating ribulose-1,5-bisphosphate or reducing 3-phosphoglycerate. Biochim Biophys Acta 848:392–401

    Article  CAS  Google Scholar 

  • Dworkin M, Foster J (1958) Experiments with some microorganisms which utilize ethane and hydrogen. J Bacteriol 75:592–601

    CAS  PubMed  Google Scholar 

  • Genty B, Briantais JM, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990:87–92

    CAS  Google Scholar 

  • Gordon SA, Weber RP (1951) Colorimetric estimation of indoleacetic acid. Plant Physiol 26:192–195

    Article  CAS  PubMed  Google Scholar 

  • Guinn G, Brummett DL, Beier RC (1986) Purification and measurement of abscisic acid and indole-acetic acid by high performance liquid chromatography. Plant Physiol 81:997–1002

    Article  CAS  PubMed  Google Scholar 

  • Hallmann J, Quadt-Hallmann A, Mahaffee WF, Kloepper JW (1997) Bacterial endophytes in agricultural crops. Can J Microbiol 43:895–914

    Article  CAS  Google Scholar 

  • Hoagland DR, Arnon DI (1950) The water culture of growing plants without soil. University of California, Berkley, CA, USA

    Google Scholar 

  • Jacobs MJ, William MB, David AG (1985) Enumeration, location, characterization of endophytic bacteria within sugar beet roots. Can J Bot 63:1262–1265

    Google Scholar 

  • Kamilova F, Kravchenko LV, Shaposhnikov AI, Azarova T, Makarova N, Lugtenberg B (2006) Organic acids, sugars, and l-tryptophan in exudates of vegetables growing on stone wool and their effects on activities of rhizosphere bacteria. Mol Plant Microbe Interact 19:250–256

    Article  CAS  PubMed  Google Scholar 

  • Labate CA, Leegood RC (1989) Influence of low temperature on respiration and contents of phosphorylated intermediates in darkened barley leaves. Plant Physiol 91:905–910

    Article  CAS  PubMed  Google Scholar 

  • Larkin RP, Hopkins DL, Martin FN (1996) Suppression of Fusarium wilt of watermelon by nonpathogenic Fusarium oxysporum and other microorganisms recovered from a disease-suppressive soil. Phytopathology 86:812–819

    Article  Google Scholar 

  • Larran S, Monaco C, Alippi HE (2004) Endophytic fungi in beet (Beta vulgaris var. esculenta L.) leaves. Adv Hortic Sci 14:193–196

    Google Scholar 

  • Latch GCM, Hunt WF, Musgrave DR (1985) Endophytic fungi affect growth of perennial ryegrass. N Z J Agric Res 28:165–168

    Google Scholar 

  • Marks S, Clay K (1990) Effects of CO2 enrichment, nutrient addition, and fungal endophyte-infection on the growth of two grasses. Oecologia 84:207–214

    Google Scholar 

  • Marks S, Clay K (1996) Physiological responses of Festuca arundinacea to fungal endophyte infection. New Phytol 133:727–733

    Article  Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid bioassays with tobacco tissue cultures. Physiol Plant 15:473–497

    Article  CAS  Google Scholar 

  • Patten CL, Glick BR (2002) Role of Pseudomonas putida indoleacetic acid in development of the host plant root system. Appl Environ Microbiol 68:3795–3801

    Article  CAS  PubMed  Google Scholar 

  • Pereira JO, Azevedo JL, Petrini O (1993) Endophytic fungi of stylosanthes: a preliminary study. Mycologia 85:362–364

    Article  Google Scholar 

  • Petrini O (1986) Taxonomy of endophytic fungi of aerial plant tissues. In: Fokkema NJ, van den Heuvel J (eds) Microbiology of the phylosphere. Cambridge University Press, Cambridge, UK, pp 175–187

    Google Scholar 

  • Pillay VK, Nowak J (1997) Inoculum density, temperature and genotype effects on in vitro growth promotion and epiphytic and endophytic colonization of tomato (Lycopersicum esculentum L.) seedlings inoculated with a pseudomonad bacterium. Can J Microbiol 43:354–361

    Article  CAS  Google Scholar 

  • Porra RJ, Thompson WA, Kriedemann PE (1989) Determination of accurate coefficients and simultaneous equations for assaying chlorophyll a and b extracted with four different solvents: verification of the concentration of chlorophyll standards by atomic absorption spectroscopy. Biochim Biophys Acta 975:384–394

    Article  CAS  Google Scholar 

  • Postma J, Rattink H (1991) Biological control of Fusarium wilt of carnation with a nonpathogenic isolate of Fusarium oxysporum. Can J Bot 70:1199–1205

    Article  Google Scholar 

  • Richardson MD, Hoveland CS, Bacon CW (1993) Photosynthesis and stomatal conductance of symbiotic and nonsymbiotic tall fescue. Crop Sci 33:145–149

    Article  Google Scholar 

  • Saikkonen K, Wali P, Helander M, Faeth SH (2004) Evolution of endophyte plant symbioses. Trends Plant Sci 9:275–280

    Article  CAS  PubMed  Google Scholar 

  • Shi YW, Lou K, Li C (2009) Isolation, quantity distribution and characterization of endophytic microorganisms within sugar beet. Afr J Biotechnol 8:835–840

    CAS  Google Scholar 

  • Srivastava A, Handa AK (2005) Hormonal regulation of fruit development: a molecular perspective. J Plant Growth Regul 24:67–82

    Article  CAS  Google Scholar 

  • Stitt M (1991) Rising CO2 levels and their potential significance for carbon flow in photosynthetic cells. Plant Cell Environ 14:741–762

    Article  CAS  Google Scholar 

  • Stone JK, Bacon CW, White JF Jr (2000) An overview of endophytic microbes: endophytism defined. In: Bacon CW, White JF Jr (eds) Microbial endophytes. Marcel Dekker, New York, USA, pp 3–29

    Google Scholar 

  • Sturz AV, Christie BR, Nowak J (2000) Bacterial endophytes: potential role in developing sustainable systems of crop production. Crit Rev Plant Sci 19:1–30

    Article  Google Scholar 

  • Taiz L, Zeiger E (1991) Auxins: growth and tropisms. In: Zeiger E (ed) Plant physiology. Hardcover. Benjamin/Cunnings Press, Menlo Park, CA, pp 398–425

    Google Scholar 

  • Tanimoto E (2005) Regulation of root growth by plant hormones—roles for auxin and gibberellins. Crit Rev Plant Sci 24:249–265

    Article  CAS  Google Scholar 

  • Vessey JK (2003) Plant growth promoting rhizobacteria as biofertilizers. Plant Soil 255:571–586

    Article  CAS  Google Scholar 

  • White JF Jr, Owens JR (1992) Stromal development and mating system of Balansia epichloe, a leaf-colonizing endophyte of warm-season grasses. Appl Environ Microbiol 58:513–519

    PubMed  CAS  Google Scholar 

  • White JF Jr, Bacon CW, Hinton DM (1997) Modifications of host cells and tissues by the biotrophic endophyte Epichloe amarillans (Clavicipitaceae; Ascomycotina). Can J Bot 75:1061–1069

    Article  Google Scholar 

  • Xie H, Pasternak JJ, Glick BR (1996) Isolation and characterization of mutants of the plant growth-promoting rhizobacterium Pseudomonas putida GR12-2 that overproduce indoleacetic acid. Curr Microbiol 32:67–71

    Article  CAS  Google Scholar 

  • Yates IE, Bacon CW, Hinton DM (1997) Effects of endophytic infection by Fusarium moniliforme on corn growth and cellular morphology. Plant Dis 81:723–728

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Kai Lou or Chun Li.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Shi, Y., Lou, K. & Li, C. Growth and photosynthetic efficiency promotion of sugar beet (Beta vulgaris L.) by endophytic bacteria. Photosynth Res 105, 5–13 (2010). https://doi.org/10.1007/s11120-010-9547-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11120-010-9547-7

Keywords

Navigation