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2015 | 37 | 01 |

Tytuł artykułu

The effects of gibberellins and mepiquat chloride on nitrogenase activity in Bradyrhizobium japonicum

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Application of plant growth regulators (PGRs) to soybean plants is known to induce changes in nitrogenase activity in root nodules, and this led us to hypothesize that PGRs would affect nitrogenase activity in free-living rhizobia cultures. Little is known about the molecular basis of the effects of PGRs on nitrogenase activity in free-living rhizobia cultures. Therefore, a comparative study was conducted on the effects of gibberellins (GA3) and mepiquat chloride (PIX), which regulate plant growth, on the nitrogenase activity of the nitrogen-fixing bacterium Bradyrhizobium japonicum. Fix and nif gene regulation and protein expression in free-living cultures of B. japonicum were investigated using real-time PCR and twodimensional electrophoresis after treatment with GA3 or PIX. GA3 treatment decreased nitrogenase activity and the relative expression of nifA, nifH, and fixA genes, but these effects were reversed by PIX treatment. As expected, several proteins involved in nitrogenase synthesis were down-regulated in the GA3-treated group. Conversely, several proteins involved in nitrogenase synthesis were upregulated in the PIX-treated group, including bifunctiona ornithine acetyltransferase/N-acetylglutamate synthase, transaldolase, ubiquinol-cytochrome C reductase iron-sulfur subunit, electron transfer flavoprotein subunit beta, and acyl-CoA dehydrogenase. Two-pot experiments were conducted to evaluate the effects of GA3 and PIX on nodulation and nitrogenase activity in Rhizobium-treated legumes. Interestingly, GA3 treatment increased nodulation and depressed nitrogenase activity, but PIX treatment decreased nodulation and enhanced nitrogenase activity. Our data show that the nif and fix genes, as well as several proteins involved in nitrogenase synthesis, are up-regulated by PIX and down-regulated by GA3, respectively, in B. japonicum.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

37

Numer

01

Opis fizyczny

Article 1723 [11 p.], fig.,ref.

Twórcy

autor
  • Agronomy College of Heilongjiang Bayi Agricultural University, 163319 Daqing, Heilonjiang, China
autor
  • Agronomy College of Heilongjiang Bayi Agricultural University, 163319 Daqing, Heilonjiang, China
autor
  • Agronomy College of Heilongjiang Bayi Agricultural University, 163319 Daqing, Heilonjiang, China
autor
  • Agronomy College of Heilongjiang Bayi Agricultural University, 163319 Daqing, Heilonjiang, China
autor
  • Agronomy College of Heilongjiang Bayi Agricultural University, 163319 Daqing, Heilonjiang, China
autor
  • Agronomy College of Heilongjiang Bayi Agricultural University, 163319 Daqing, Heilonjiang, China
autor
  • Agronomy College of Heilongjiang Bayi Agricultural University, 163319 Daqing, Heilonjiang, China
autor
  • Crop Tillage and Cultivation Institute, Hei Long Jiang Academy of Agricultural Sciences, 150086 Harbin, Heilonjiang, China

Bibliografia

  • Akkose S, Gunduz U, Yucel M, Eroglu I (2009) Effects of ammonium ion, acetate and aerobic conditions on hydrogen production and expression levels of nitrogenase genes in Rhodobacter sphaeroides OU 001. Int J Hydrog Energy 34:8818–8827
  • Albrecht SL, Bennett JM, Boote KJ (1984) Relationship of nitrogenase activity to plant water stress in field-grown soybeans. FieldCrops Res 8:61–71
  • Aldea MR (2013) Identification of novel regulatory mechanisms controlling heterocyst development in Anabaena Sp. strain PCC 7120
  • Alloisio N, Felix S, Marechal J, Pujic P, Rouy Z, Vallenet D, Medigue C, Normand P (2007) Frankia alni proteome under nitrogen-fixing and nitrogen-replete conditions. Physiol Plant 130:440–453
  • Atzorn R, Crozier A, Wheeler CT, Sandberg G (1988) Production of gibberellins and indole-3-acetic acid by Rhizobium phaseoli in relation to nodulation of Phaseolus vulgaris roots. Planta 175:532–538
  • Bianco C, Defez R (2010) Auxins upregulate nif and fix genes. Plant Signal Behav 5:1290–1294
  • Chohan SN, Copeland L (1998) Acetoacetyl coenzyme A reductase and polyhydroxybutyrate synthesis in rhizobium (Cicer) sp. Strain CC 1192. Appl Environ Microbiol 64:2859–2863
  • Dart PJ, Day JM (1971) Effects of incubation temperature and oxygen tension on nitrogenase activity of legume root nodules. Plant Soil 35:167–184
  • De Ley J, Doudoroff M (1957) The metabolism of D-galactose in Pseudomonas saccharophila. J Biol Chem 227:745–757
  • Dhir KK, Rao L, Singh KJ, Chark KS (1992) Effect of phenolic compounds on symbiotic nitrogen fixation in pigeonpea (Cajanus cajan (L.) Millsp.). Biol Plant 34:409–413
  • Ding Y, Kalo P, Yendrek C, Sun J, Liang Y, Marsh JF, Harris JM, Oldroyd GE (2008) Abscisic acid coordinates nod factor and cytokinin signaling during the regulation of nodulation in Medicago truncatula. Plant Cell Online 20:2681–2695
  • Dixon R, Kahn D (2004) Genetic regulation of biological nitrogen fixation. Nat Rev Microbiol 2:621–631
  • Earl CD, Ronson CW, Ausubel FM (1987) Genetic and structural analysis of the Rhizobium meliloti fixA, fixB, fixC, and fixX genes. J Bacteriol 169:1127–1136
  • Egamberdiyeva D, Flich G (2004) Effect of plant growth-promoting bacteria on growth and nutrient uptake of cotton and pea in a semi-arid region of Uzbekistan. J Arid Environ 56:293–301
  • Ehira S, Ohmori M (2006) NrrA, a nitrogen-responsive response regulator facilitates heterocyst development in the cyanobacterium Anabaena sp. strain PCC 7120. Mol Microbiol 59:1692–1703
  • Emongor V (2007) Gibberellic acid (GA3) influence on vegetative growth, nodulation and yield of cowpea (Vigna unquiculata (L.) Walp.). J Agron 6:509–517
  • Ferguson BJ, Ross JJ, Reid JB (2005) Nodulation phenotypes of gibberellin and brassinosteroid mutants of pea. Plant Physiol 138:2396–2405
  • Fischer H (1994) Genetic regulation of nitrogen fixation in rhizobia. Microbiol Rev 58:352
  • Francisco PB Jr, Akao S, Kokubun M (1991) The timing of exogenous 2, 4-dichlorophenoxyacetate (2, 4-D) application affects nodulation of soybeans, glycine max (L.) merr. Soil Sci Plant Nutr 37:707–714
  • Fukuhara H, Minakawa Y, Akao S, Minamisawa K (1994) The involvement of indole-3-acetic acid produced by Bradyrhizobium elkanii in nodule formation. Plant Cell Physiol 35:1261–1265
  • Ghyselinck J, Pfeiffer S, Heylen K, Sessitsch A, De Vos P (2013) The effect of primer choice and short read sequences on the outcome of 16S rRNA gene based diversity studies. PLoS One 8:e71360
  • Hallenbeck PC, Meyer CM, Vignais PM (1982) Regulation of nitrogenase in the photosynthetic bacterium Rhodopseudomonas capsulata as studied by two-dimensional gel electrophoresis. J Bacteriol 151:1612–1616
  • Heggo A, Angle JS, Chaney RL (1990) Effects of vesiculararbuscular mycorrhizal fungi on heavy metal uptake by soybeans. Soil Biol Biochem 22:865–869
  • Heinrich A, Maheswaran M, Ruppert U, Forchhammer K (2004) The Synechococcus elongatus P signal transduction protein controls arginine synthesis by complex formation with N-acetyl-Lglutamate kinase. Mol Microbiol 52:1303–1314
  • Hirsch AM, Bhuvaneswari TV, Torrey JG, Bisseling T (1989) Early nodulin genes are induced in alfalfa root outgrowths elicited by auxin transport inhibitors. Proc Natl Acad Sci 86:1244–1248
  • Imperlini E, Bianco C, Lonardo E, Camerini S, Cermola M, Moschetti G, Defez R (2009) Effects of indole-3-acetic acid on Sinorhizobium meliloti survival and on symbiotic nitrogen fixation and stem dry weight production. Appl Microbiol Biotechnol 83:727–738
  • Islas-Flores T, Guillén G, Alvarado-Affantranger X, Lara-Flores M, Sánchez F, Villanueva MA (2011) PvRACK1 loss-of-function impairs cell expansion and morphogenesis in Phaseolus vulgaris L. root nodules. Mol Plant Microbe Interact 24:819–826
  • Leite VM, Rosolem CR, Rodrigues JD (2003) Gibberellin and cytokinin effects on soybean growth. Sci Agric (Piracicaba, Braz.) 60:55–59
  • Li X, Liu T, Wu Y, Zhao G, Zhou Z (2010) Derepressive effect of NH4⁺ on hydrogen production by deleting the glnA1 gene in Rhodobacter sphaeroides. Biotechnol Bioeng 106:564–572
  • Li WX, Chen M, Chen WT, Qiao CK, Li MH, Han LJ (2012) Determination of mepiquat chloride in cotton crops and soil and its dissipation rates. Ecotoxicol Environ Saf 85:137–143
  • Lievens S, Goormachtig S, Den Herder J, Capoen W, Mathis RE, Hedden P, Holsters M (2005) Gibberellins are involved in nodulation of Sesbania rostrata. Plant Physiol 139:1366–1379
  • Maekawa T, Maekawa-Yoshikawa M, Takeda N, Imaizumi-Anraku H, Murooka Y, Hayashi M (2009) Gibberellin controls the nodulation signaling pathway in Lotus japonicus. Plant J 58:183–194
  • Mao DP, Zhou Q, Chen CY, Quan ZX (2012) Coverage evaluation of universal bacterial primers using the metagenomic datasets. BMC Microbiol 12:66
  • Morandi EN, Casano LM, Nakayama F (1983) Effect of N-N dimethyl pipredinium chloride (PIX) and 2-chloroethy trimethyl ammonium chloride (CCC) on growth, yield and dry matter partitioning of soybean plants grown under two environmental condition. Phyton Argentina 44:133–144
  • Nagarajan T, Vanderleyden J, Tripathi AK (2007) Identification of salt stress inducible genes that control cell envelope related functions in Azospirillum brasilense Sp7. Mol Genet Genomics 278:43–51
  • Oger E, Marino D, Guigonis J, Pauly N, Puppo A (2012) Sulfenylated proteins in theMedicago truncatula–Sinorhizobium meliloti symbiosis. J Proteomics 75:4102–4113
  • Prasad BN (2000) Effect of different PGRs on cuttings, seed germination, photosynthetic pigments and nitrogen fixation in Alnus nepalensis. In: Bista MS, Joshi RB, Amatya SM, Parajuli AV, Adhikari MK, Saiju HK, Thakur R, Suzuki K, Ishii K (eds) Bio-technology applications for reforestation and biodiversity conservation. Proceedings of the 8th International Workshop of BIO-REFOR, Kathmandu, Nepal, pp 77–82
  • Qureshi MI, Muneer S, Bashir H, Ahmad J, Iqbal M (2010) Nodule physiology and proteomics of stressed legumes. Adv Bot Res 56:1–48
  • Sarkar A, Kohler JOR, Hurek T, Reinhold-Hurek B (2012) A novel regulatory role of the Rnf complex of Azoarcus sp. strain BH72. Mol Microbiol 83:408–422
  • Schmeisser C, Liesegang H, Krysciak D, Bakkou N, Le Quéré A, Wollherr A et al (2009) Rhizobium sp. strain NGR234 possesses a remarkable number of secretion systems. Appl Environ Microbiol 75:4035–4045
  • Seefeldt LC, Hoffman BM, Dean DR (2009) Mechanism of Modependent nitrogenase. Annu Rev Biochem 78:701
  • Stearn WC, Miller RH, Cakmakci L et al (1980) Possible effects of plant growth regulators on competitiveness of Rhizobium spp. In: Agronomy Abstracts. 72nd annual meeting, American Society of Agronomy
  • Stefan W, Anke B, Ildefonso B, Sebastian J, Javier L, Isabel M, Alfred P, José ER, Susanne SB, Rafael S, José MV, Susanne Z, Michael G (2012) Genome sequence of the soybean symbiont Sinorhizobium fredii HH103. J Bacteriol 194:1617–1618
  • Summers ML, Denton MC, McDermott TR (1999) Genes coding for phosphotransacetylase and acetate kinase in Sinorhizobium meliloti are in an operon that is inducible by phosphate stress and controlled by phoB. J Bacteriol 181:2217–2224
  • Walshaw DL, Wilkinson A, Mundy M, Smith M, Poole PS (1997) Regulation of the TCA cycle and the general amino acid permease by overflow metabolism in Rhizobium leguminosarum. Microbiology 143:2209–2221
  • Weimin Y (2000) The Research Progress and Survey on Communications with Chaos [J]. J Guilin Inst Electron Technol 1:14
  • Yamazaki S, Nomata J, Fujita Y (2006) Differential operation of dual protochlorophyllide reductases for chlorophyll biosynthesis in response to environmental oxygen levels in the cyanobacterium Leptolyngbya boryana. Plant Physiol 142:911–922
  • Yoch DC (1979) Manganese, an essential trace element for N2 fixation by Rhodospirillum rubrum and Rhodopseudomonas capsulata: role in nitrogenase regulation. J Bacteriol 140:987–995
  • York AC (1983) Response of cotton to mepiquat chloride with varying N rates and plant populations. Agron J 75:667–672
  • Zhang Z, Shu W, Liao W, Lan C (2002) Role of Legume species in revegetation of mined wastelands. Chin J Ecol 2:11
  • Zhang X, Zhai R, Zheng D, Feng N, Qi Q (2010) Effects of plant growth regulators (PGRs) on nitrogen metabolism related indicators in soybean roots. Soybean Sci 3:20
  • Zhao W, Ye Z, Zhao J (2007) RbrA, a cyanobacterial rubrerythrin, functions as a FNR-dependent peroxidase in heterocysts in protection of nitrogenase from damage by hydrogen peroxide in Anabaena sp. PCC 7120. Mol Microbiol 66:1219–1230

Typ dokumentu

Bibliografia

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Identyfikator YADDA

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