Phosphatase Activities of Root-nodule Bacteria and Nutritional Factors Affecting Production of Phosphatases by Representative Bacteria from Three Different Genera
Main Article Content
Abstract
Fifty six strains of root-nodule bacteria isolated from 3 medicinal legumes including Indigofera
tinctoria L., Derris elliptica Benth. and Pueraria mirifica Airy Shaw & Suvat. were measured for
their acid-, neutral- and alkaline phosphatase activities. All strains produced extracellular
phosphatases, while almost no cell-bound phosphatase activities were observed. The unidentified
strain DASA 68062 and Bradyrhizobium sp. DASA 64011 produced the highest activity of acid
phosphatase, the unidentified strain DASA 68032 and Bradyrhizobium sp. DASA 68056 produced
the highest activity of neutral phosphatase and the strain DASA 68056 also produced the highest
activity of alkaline phosphatase which differed significantly from other strains. Effects of 14
nutritional factors on production of phosphatases by the strain DASA 57020 in
Ralstonia/Cupriavidus group, Bradyrhizobium sp. DASA 68056 and Rhizobium sp. DASA 68066
were determined. The stimulation of extracellular acid-, neutral- and alkaline phosphatase
activities of the strain DASA 57020 occurred when the strain utilized D-fructose, D-xylose and Dmannitol
as sole carbon sources and urea as a sole nitrogen source. The significant increase of
extracellular acid-, neutral- and alkaline phosphatase activities of the strain DASA 68056 was
detected in the presence of D-fructose and D-xylose. The factors including D-fructose, sucrose and
KNO3 could increase extracellular acid-, neutral- and alkaline phosphatase activities of the strain
DASA 68066. The carbon source, D-fructose, was the only factor that induced production of acid-,
neutral- and alkaline phosphatases by all strains tested.
Keywords: acid phosphatase, alkaline phosphatase, neutral phosphatase, root-nodule bacteria
* Corresponding author: Tel: 66-34-255093 Fax: 66-34-273045
E-mail: neelawan@su.ac.th
Article Details
Copyright Transfer Statement
The copyright of this article is transferred to Current Applied Science and Technology journal with effect if and when the article is accepted for publication. The copyright transfer covers the exclusive right to reproduce and distribute the article, including reprints, translations, photographic reproductions, electronic form (offline, online) or any other reproductions of similar nature.
The author warrants that this contribution is original and that he/she has full power to make this grant. The author signs for and accepts responsibility for releasing this material on behalf of any and all co-authors.
Here is the link for download: Copyright transfer form.pdf
References
isolated from Tianmu Mountain, Zhejiang, China, World Journal of Microbiology and
Biotechnology, 22 (9), 983-990.
[2] Wilson, M. A. and Metcalf, W. W. 2005. Genetic diversity and horizontal transfer of genes
involved in oxidation of reduced phosphorus compounds by Alcaligenes faecalis WM2072,
Applied and Environmental Microbiology, 71 (1), 290-296.
[3] Goldstein, A. H. 1986. Bacterial solubilization of mineral phosphates: historical perspectives
and future prospects, American Journal of Alternative Agriculture, 1 (2), 51-57.
[4] Chen, Y. P., Rekha, P. D., Arun, A. B., Shen, F. T., Lai, W. A. and Young, C. C. 2006.
Phosphate solubilizing bacteria from subtropical soil and their tricalcium phosphate
solubilzing abilities, Applied Soil Ecology, 34 (1), 33-41.
[5] Datta, M., Banish, S. and Dupta, R. K. 1982. Studies on the efficacy of a phytohormone
producing phosphate solubilizing Bacillus firmus in augmenting paddy yield in acid soils of
Nagaland, Plant and Soil, 69 (3), 365-373.
[6] Kim, K. Y., Jordan D. and McDonald, G. A. 1998. Enterobacter agglomerans, phosphate
solubilizing bacteria, and microbial activity in soil: effect of carbon sources, Soil Biology and
Biochemistry, 30 (8/9), 995-1003.
[7] Chung, H., Park, M., Madhaiyan, M., Seshadri, S., Song, J., Cho, H. and Sa, T. 2005.
Isolation and characterization of phosphate solubilizing bacteria from the rhizosphere of crop
plants of Korea, Soil Biology and Biochemistry, 37 (10), 1970-1974.
[8] El-Azouni, I. M. 2008. Effect of phosphate solubilizing fungi on growth and nutrient uptake
of soybean (Glycine max L.) plants, Journal of Applied Sciences Research, 4 (6), 592-598.
[9] Kapri, A. and Tewari, L. 2010. Phosphate solubilization potential and phosphatase activity
of rhizospheric Trichoderma spp., Brazilian Journal of Microbiology, 41 (3), 787-795.
[10] Ponmurugan, P. and Gopi, C. 2006. In vitro production of growth regulators and phosphate
activity by phosphate solubilizing bacteria, African Journal of Biotechnology, 5 (4), 348-350.
[11] Relwani, L., Krishna, P. and Reddy, M. S. 2008. Effect of carbon and nitrogen sources on
phosphate solubilization by a wild-type strain and UV-induced mutants of Aspergillus
tubingensis, Current Microbiology, 57 (5), 401-406.
KMITL Sci. Tech. J. Vol. 9 No. 2 Jul. - Dec. 2009
82
[12] Kim, K. Y., Jordan, D. and Mc Donald, G. A. 1998. Enterobacter agglomerans, phosphate
solubilizing bacteria, and microbial activity in soil: effect of carbon sources, Soil Biology and
Biochemistry, 30(8/9), 995-1003.
[13] Sabannavar, S. J. and Lakshman, H. C. 2009. Effect of rock phosphate solubilization using
mycorrhizal fungi and phosphobacteria on two high yielding varieties of Sesamum indicum
L., World Journal of Agricultural Sciences, 5(4), 470-479.
[14] Rodriguez, H., Fraga1, R., Gonzalez1, T. and Bashan, Y. 2006. Genetics of phosphate
solubilization and its potential applications for improving plant growth-promoting bacteria,
Plant and Soil, 287(1/2), 15-21.
[15] Mobley, D. M., Chengappa, M. M., Kadel, W. L. and Stuart, J. G. 1984. Effect of pH,
temperature and media on acid and alkaline phosphatase activity in "clinical" and
"nonclinical" isolates of Bordetella bronchiseptica, Canadian Journal of Comparative
Medicine, 48(2), 175–178.
[16] Ishihara , K. and Kuramitsu, H. K. 1995. Cloning and expression of a neutral phosphatase
gene from Treponema denticola, Infection and Immunity, 63(4), 1147-1152.
[17] Pongsilp, N. and Nuntagij, A. 2009. Genetic diversity and metabolites production of rootnodule
bacteria isolated from medicinal legumes Indigofera tinctoria, Pueraria mirifica and
Derris elliptica Benth. grown in different geographic origins across Thailand, American-
Eurasian Journal of Agricultural and Environmental Sciences, 6(1), 26-34.
[18] Leelahawonge, C., Nuntagij, A., Teaumroong, N., Boonkerd, N. and Pongsilp, N. 2010.
Characterization of root-nodule bacteria isolated from the medicinal legume Indigofera
tinctoria, Annals of Microbiology, 60(1), 65-74.
[19] Pongsilp, N. and Leelahawonge, C. 2010. Root-nodule symbionts of Derris elliptica Benth.
are members of three distinct genera Rhizobium, Sinorhizobium and Bradyrhizobium,
International Journal of Integrative Biology, 9(1), 37-42.
[20] Pongsilp, N., Leelahawonge, C., Nuntagij, A., Teaumroong, N. and Boonkerd, N. 2010.
Characterization of Pueraria mirifica-nodulating rhizobia present in Thai soil, African
Journal of Microbiology Research, 4(12), 1307-1313.
[21] Keele Jr., B. B., Hamilton, P. B. and Elkan, G. H. 1969. Glucose catabolism in Rhizobium
japonicum, Journal of Bacteriology, 97(3), 1184-1191.
[22] Pikovskaya, R. I. 1948. Mobilization of phosphorus in soils in connection with vital activity
of some microbial species, Microbiologia, 17, 362-370.
[23] Pantujit, S. and Pongsilp, N. 2010. Phosphatase activity and affects of phosphate-solubilizing
bacteria on yield and uptake of phosphorus in corn, World Applied Sciences Journal, 8(4),
429-435.
[24] Tso, S. C. and Chen, Y. R. 1997. Isolation and characterization of a group III isozyme of acid
phosphatase from rice plants, Botanical Bulletin of Academia Sinica, 38, 245-250.
[25] Vinter, V., Smid, F. and Smrckova, I. 1987. Factors influencing the activity of cellular
alkaline phosphatase during growth and sporulation of Bacillus subtilis, Folia
Microbiologica, 32(2), 89-95.
[26] Oh, W. S., Im, Y. S., Yeon, K. Y., Yoon, Y. J. and Kim, J. W. 2007. Phosphate and carbon
source regulation of alkaline phosphatase and phospholipase in Vibrio vulnificus, Journal of
Microbiology, 5(4), 311-317.
[27] Bandyopadhyay, S. Kr. and Majumdar, S. K. 1974. Regulation of the formation of alkaline
phosphatase during neomycin biosynthesis, Antimicrobial Agents and Chemotherapy, 5(4),
431-434.
[28] Fraenkel, D. G. and Horecker, B. L. 1965. Fructose-1,6-diphosphatase and acid hexose
phosphatase of Escherichia coli, Journal of Bacteriology, 90(4), 837-842.