Please wait a minute...
Frontiers in Biology

ISSN 1674-7984

ISSN 1674-7992(Online)

CN 11-5892/Q

Front. Biol.    2016, Vol. 11 Issue (6) : 481-487    https://doi.org/10.1007/s11515-016-1426-y
RESEARCH ARTICLE
Rhizoplane microbiota of superior wheat varieties possess enhanced plant growth-promoting abilities
Ayesha Siddiqa1,Yasir Rehman1(),Shahida Hasnain1,2
1. Department of Microbiology and Molecular Genetics, University of the Punjab, Lahore, Pakistan
2. The Women University Multan, Multan, Pakistan
 Download: PDF(770 KB)   HTML
 Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks
Abstract

BACKGROUND: Microbes affect the growth of plants. In this study, the diversity and plant growth-supporting activities of wheat rhizospheric bacteria were examined.

METHODS: Sampling was performed thrice at different phases of plant growth. Microbes associated with the rhizoplane of three wheat varieties (Seher, Lasani, and Faisalabad) were cultured and assessed for their plant growth-promoting abilities based on auxin production, hydrogen cyanide production, phosphate solubilization, and nitrogen fixation.

RESULTS: Bacterial load (CFU/mL) declined, and the succession of bacterial diversity occurred as the plants aged. Most auxin-producing bacteria and the highest concentrations of auxin (77 µg/mL) were observed during the second sampling point at the tillering stage. The Seher variety harbored the most auxin-producing as well as phosphate-solubilizing bacteria. Most of the bacteria belonged to Bacillus and Pseudomonas. Planomicrobium, Serratia, Rhizobium, Brevundimonas, Stenotrophomonas, and Exiguobacterium sp. were also found.

CONCLUSIONS: These results suggest that the rhizoplane microbiota associated with higher-yield plant varieties have better plant growth-promoting abilities as compared to the microbiota associated with lower-yield plant varieties.

Keywords wheat      microbiota      rhizoplane      auxin      phosphate solubilization     
Corresponding Author(s): Yasir Rehman   
Online First Date: 01 December 2016    Issue Date: 26 December 2016
 Cite this article:   
Ayesha Siddiqa,Yasir Rehman,Shahida Hasnain. Rhizoplane microbiota of superior wheat varieties possess enhanced plant growth-promoting abilities[J]. Front. Biol., 2016, 11(6): 481-487.
 URL:  
https://academic.hep.com.cn/fib/EN/10.1007/s11515-016-1426-y
https://academic.hep.com.cn/fib/EN/Y2016/V11/I6/481
Fig.1  Auxin production by bacterial isolates of the rhizoplanes of three wheat varieties (Seher, Faisalabad, and Lasani) at the first sampling point. Most auxin producers were found in the rhizoplane of the Faisalabad variety. The highest auxin concentration was observed for LAR1-4 from the Lasani variety.

(SHR= Seher, FDR= Faisalabad, LAR= Lasani)

Fig.2  Auxin production by bacterial isolates of the rhizoplanes of three wheat varieties (Seher, Faisalabad, and Lasani) at the second sampling point. Most auxin producers were found in the rhizoplane of the Seher variety at the second sampling point, but highest auxin concentration was observed for FDR2-4 from the Faisalabad variety.

(SHR= Seher, FDR= Faisalabad, LAR= Lasani)

Fig.3  Auxin production by bacterial isolates of the rhizoplanes of three wheat varieties (Seher, Faisalabad, and Lasani) at the third sampling point. Most auxin producers were again detected in the rhizoplane of the Seher variety. The highest auxin concentration was observed for SHR3-5.

(SHR= Seher, FDR= Faisalabad, LAR= Lasani)

Fig.4  Neighbor-joining phylogenetic tree of the 16S rRNA gene sequences of the selected bacterial isolates. The tree was constructed by aligning the sequences and their nearest homologous sequences from NCBI using Mega 5. One hundred bootstrap replicates were used to measure reliability. Most of the bacterial isolates were identified as Firmicutes.

(SHR= Seher, FDR= Faisalabad, LAR= Lasani)

1 Asanuma S, Tanaka H, Yatazawa M (1979). Rhizoplane microorganisms of rice seedlings as examined by scanning electron microscopy. Soil Sci Plant Nutr, 25(4): 539–551
https://doi.org/10.1080/00380768.1979.10433195
2 Benson H J (2005). Bensonʼs microbiological applications: laboratory manual in general microbiology. Boston: McGraw-Hill Higher Education
3 Berg G (2009). Plant-microbe interactions promoting plant growth and health: perspectives for controlled use of microorganisms in agriculture. Appl Microbiol Biotechnol, 84(1): 11–18
https://doi.org/10.1007/s00253-009-2092-7 pmid: 19568745
4 Bernbom N, Ng Y Y, Kjelleberg S, Harder T, Gram L (2011). Marine bacteria from Danish coastal waters show antifouling activity against the marine fouling bacterium Pseudoalteromonas sp. strain S91 and zoospores of the green alga Ulva australis independent of bacteriocidal activity. Appl Environ Microbiol, 77(24): 8557–8567
https://doi.org/10.1128/AEM.06038-11 pmid: 22003011
5 Cappuccino J G, Sherman N (2007). Microbiology: A Laboratory Manual. USA: Pearson Benjamin Cummings
6 Curl E A, Truelove B (1986). The rhizosphere. Berlin: Springer-Verlag
7 Felsenstein J (1985). Confidence limits on phylogenies: an approach using the Bootstrap. Evolution, 39(4): 783–791
https://doi.org/10.2307/2408678
8 Goldstein A H (1986). Bacterial solubilization of mineral phosphates: Historical perspective and future prospects. Am J Altern Agric, 1(02): 51–57
https://doi.org/10.1017/S0889189300000886
9 Gordon S A, Weber R P (1951). Colorimetric estimation of indole acetic acid. Plant Physiol, 26(1): 192–195
https://doi.org/10.1104/pp.26.1.192 pmid: 16654351
10 Iqbal U, Jamil N, Ali I, Hasnain S (2010). Effect of zinc-phosphate-solubilizing bacterial isolates on growth of Vigna radiata. Ann Microbiol, 60(2): 243–248
https://doi.org/10.1007/s13213-010-0033-4
11 Khan Z, Kim S G, Jeon Y H, Khan H U, Son S H, Kim Y H (2008). A plant growth promoting Rhizobacterium, Paenibacillus polymyxa strain GBR-1, suppresses root-knot nematode. Bioresour Technol, 99(8): 3016–3023
https://doi.org/10.1016/j.biortech.2007.06.031 pmid: 17706411
12 Lægreid M, Bøckman O C, Kaarstad O (1999). Agriculture, fertilizers, and the environment. Euro J Soil Sci, 51(3): 541–549 DOI: 10.1046/j.1365-2389.2000.00334-2.x
13 Lorck H (1948). Production of hydrocyanic acid by bacteria. Physiol Plant, 1(2): 142–146
https://doi.org/10.1111/j.1399-3054.1948.tb07118.x
14 Porsby C H, Nielsen K F, Gram L (2008). Phaeobacter and Ruegeria species of the Roseobacter clade colonize separate niches in a Danish Turbot (Scophthalmus maximus)-rearing farm and antagonize Vibrio anguillarum under different growth conditions. Appl Environ Microbiol, 74(23): 7356–7364
https://doi.org/10.1128/AEM.01738-08 pmid: 18952864
15 Qureshi M A, Ahmad Z A, Akhtar N, Iqbal A, Mujeeb F, Shakir M A (2012). Role of phosphate solubilizing bacteria (Psb) in enhancing p availability and promoting cotton growth. J Anim Plant Sci., 22: 204–210
16 Rodríguez H, Fraga R (1999). Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol Adv, 17(4-5): 319–339
https://doi.org/10.1016/S0734-9750(99)00014-2 pmid: 14538133
17 Saitou N, Nei M (1987). The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol, 4(4): 406–425
pmid: 3447015
18 Sylvia D M, Fuhrmann J J, Hartel P, Zuberer D A (2005). Principles and applications of soil microbiology. New Age Intern, 31(2): 11–68
19 Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011). MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol, 28(10): 2731–2739
https://doi.org/10.1093/molbev/msr121 pmid: 21546353
20 Teale W D, Paponov I A, Palme K (2006). Auxin in action: signalling, transport and the control of plant growth and development. Nat Rev Mol Cell Biol, 7(11): 847–859
https://doi.org/10.1038/nrm2020 pmid: 16990790
21 Tilman D, Cassman K G, Matson P A, Naylor R, Polasky S (2002). Agricultural sustainability and intensive production practices. Nature, 418(6898): 671–677
https://doi.org/10.1038/nature01014 pmid: 12167873
22 Vessey J K (2003). Plant growth promoting rhizobacteria as biofertilizers. Plant Soil, 255(2): 571–586
https://doi.org/10.1023/A:1026037216893
[1] FIB-10426-OF-YR_suppl_1 Download
[1] Johanna Morrow, Kyle T. Willenburg, Emmanuel Liscum. Phototropism in land plants: Molecules and mechanism from light perception to response[J]. Front. Biol., 2018, 13(5): 342-357.
[2] Zhaopei ZHANG, Liyuan NIU, Xiling CHEN, Xu XU, Zhengang RU. Improvement of plant cryosection[J]. Front Biol, 2012, 7(4): 374-377.
[3] Peng ZHAO, Dong-Qiao SHI, Wei-Cai YANG. Patterning the embryo in higher plants: Emerging pathways and challenges[J]. Front Biol, 2011, 06(01): 3-11.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed