참고문헌
- Batjes NH. 1997. A world dataset of derived soil properties by FAO-UNESCO soil unit for global modelling. Soil Use Manage. 13: 9-16. https://doi.org/10.1111/j.1475-2743.1997.tb00550.x
- Rodríguez H, Fraga R. 1999. Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol. Adv. 17: 319-339. https://doi.org/10.1016/S0734-9750(99)00014-2
- Khan MS, Zaidi A, Wani PA. 2007. Role of phosphate-solubilizing microorganisms in sustainable agriculture - a review. Agron. Sustain. Dev. 27: 29-43. https://doi.org/10.1051/agro:2006011
- Thomas L, Hodgson DA, Wentzel A, Nieselt K, Ellingsen TE, Moore J, et al. 2012. Metabolic switches and adaptations deduced from the proteomes of Streptomyces coelicolor wild type and phoP mutant grown in batch culture. Mol. Cell. Proteomics 11: M111.013797. https://doi.org/10.1074/mcp.M111.013797
- Buch A, Archana G, Naresh Kumar G. 2008. Metabolic channeling of glucose towards gluconate in phosphate-solubilizing Pseudomonas aeruginosa P4 under phosphorus deficiency. Res. Microbiol. 159: 635-642. https://doi.org/10.1016/j.resmic.2008.09.012
- Mander C, Wakelin S, Young S, Condron L, O'Callaghan M. 2012. Incidence and diversity of phosphate-solubilising bacteria are linked to phosphorus status in grassland soils. Soil Biol. Biochem. 44: 93-101. https://doi.org/10.1016/j.soilbio.2011.09.009
- Goldstein AH, Liu ST. 1987. Molecular cloning and regulation of a mineral phosphate solubilizing gene from Erwinia herbicola. Nat. Biotechnol. 5: 72-74. https://doi.org/10.1038/nbt0187-72
- Mikanova O, Novakova J. 2002. Evaluation of the P-solubilizing activity of soil microorganisms and its sensitivity to soluble phosphate. Rostlinna Vyroba 48: 397-400.
- Chen Y, Rekha P, Arun A, Shen F, Lai W-A, Young C. 2006. Phosphate solubilizing bacteria from subtropical soil and their tricalcium phosphate solubilizing abilities. Appl. Soil Ecol. 34: 33-41. https://doi.org/10.1016/j.apsoil.2005.12.002
- Patel DK, Archana G, Kumar GN. 2008. Variation in the nature of organic acid secretion and mineral phosphate solubilization by Citrobacter sp. DHRSS in the presence of different sugars. Curr. Microbiol. 56: 168-174. https://doi.org/10.1007/s00284-007-9053-0
- Oubrie A, Rozeboom HJ, Kalk KH, Olsthoorn AJ, Duine JA, Dijkstra BW. 1999. Structure and mechanism of soluble quinoprotein glucose dehydrogenase. EMBO J. 18: 5187-5194. https://doi.org/10.1093/emboj/18.19.5187
- Lessie T, Phibbs Jr P. 1984. Alternative pathways of carbohydrate utilization in pseudomonads. Annu. Rev. Microbiol. 38: 359-388. https://doi.org/10.1146/annurev.mi.38.100184.002043
- Zeng Q, Wu X, Wen X. 2016. Effects of soluble phosphate on phosphate-solubilizing characteristics and expression of gcd gene in Pseudomonas frederiksbergensis JW-SD2. Curr. Microbiol. 72: 198-206. https://doi.org/10.1007/s00284-015-0938-z
- Gyaneshwar P, Parekh L, Archana G, Poole P, Collins M, Hutson R, Kumar GN. 1999. Involvement of a phosphate starvation inducible glucose dehydrogenase in soil phosphate solubilization by Enterobacter asburiae. FEMS Microbiol. Lett. 171: 223-229. https://doi.org/10.1111/j.1574-6968.1999.tb13436.x
- Ishige T, Krause M, Bott M, Wendisch VF, Sahm H. 2003. The phosphate starvation stimulon of Corynebacterium glutamicum d etermined by DNA m icroarray analy ses. J. Bacteriol. 185: 4519-4529. https://doi.org/10.1128/JB.185.15.4519-4529.2003
- Pragai Z, Allenby NE, O'Connor N, Dubrac S, Rapoport G, Msadek T, Harwood CR. 2004. Transcriptional regulation of the phoPR operon in Bacillus subtilis. J. Bacteriol. 186: 1182-1190. https://doi.org/10.1128/JB.186.4.1182-1190.2004
- Mahenthiralingam E, Bischof J, Byrne SK, Radomski C, Davies JE, Av-Gay Y, Vandamme P. 2000. DNA-based diagnostic approaches for identification of Burkholderia cepacia complex, Burkholderia vietnamiensis, Burkholderia multivorans, Burkholderia stabilis, and Burkholderia cepacia genomovars I and III. J. Clin. Microbiol. 38: 3165-3173.
- LiPuma JJ, Spilker T, Gill LH, Campbell III PW, Liu L, Mahenthiralingam E. 2001. Disproportionate distribution of Burkholderia cepacia complex species and transmissibility markers in cystic fibrosis. Am. J. Respir. Crit. Care Med. 164: 92-96. https://doi.org/10.1164/ajrccm.164.1.2011153
- Nishiy ama E, Ohtsubo Y , Nagata Y , Tsuda M. 2010. Identification of Burkholderia multivorans ATCC 17616 genes induced in soil environment by in vivo expression technology. Environ. Microbiol. 12: 2539-2558.
- Vermis K, Brachkova M, Vandamme P, Nelis H. 2003. Isolation of Burkholderia cepacia complex genomovars from waters. Syst. Appl. Microbiol. 26: 595-600. https://doi.org/10.1078/072320203770865909
- Mendes R, Pizzirani-Kleiner AA, Araujo WL, Raaijmakers JM. 2007. Diversity of cultivated endophytic bacteria from sugarcane: genetic and biochemical characterization of Burkholderia cepacia complex isolates. Appl. Environ. Microbiol. 73: 7259-7267. https://doi.org/10.1128/AEM.01222-07
- Hou L. 2012. Studies on screening of efficient phosphate-solubilizing bacteria in the rhizosphere of pine trees and on their characteristics. Master Thesis, Nanjing Forestry University, Nanjing, China.
- Li G-X, Wu X-Q, Ye J-R. 2013. Biosafety and colonization of Burkholderia multivorans WS-FJ9 and its growth-promoting effects on poplars. Appl. Microbiol. Biotechnol. 97: 10489-10498. https://doi.org/10.1007/s00253-013-5276-0
- Ames BN. 1966. Assay of inorganic phosphate, total phosphate and phosphatase. Methods Enzymol. 8: 115-118.
- Kang S, Denman SE, Morrison M, Yu Z, McSweeney CS. 2009. An efficient RNA extraction method for estimating gut microbial diversity by polymerase chain reaction. Curr. Microbiol. 58: 464-471. https://doi.org/10.1007/s00284-008-9345-z
- Grabherr MG, Haas BJ, Yassour M, Levin JZ, Thompson DA, Amit I, et al. 2011. Full-length transcriptome assembly from RNA-Seq data without a reference genome. Nat. Biotechnol. 29: 644-652. https://doi.org/10.1038/nbt.1883
- Conesa A, Gotz S, Garcia-Gomez JM, Terol J, Talon M, Robles M. 2005. Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics 21: 3674-3676. https://doi.org/10.1093/bioinformatics/bti610
- Kanehisa M, Goto S. 2000. KEGG: Kyoto Encyclopedia of Genes and Genomes. Nucleic Acids Res. 28: 27-30. https://doi.org/10.1093/nar/28.1.27
- Mortazavi A, Williams BA, McCue K, Schaeffer L, Wold B. 2008. Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat. Methods 5: 621-628. https://doi.org/10.1038/nmeth.1226
- Audic S, Claverie J-M. 1997. The significance of digital gene expression profiles. Genome Res. 7: 986-995. https://doi.org/10.1101/gr.7.10.986
-
Livak KJ, Schmittgen TD. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the
$2-{\Delta}{\Delta}CT$ method. Methods 25: 402-408. https://doi.org/10.1006/meth.2001.1262 - Lukowitz W, Nickle TC, Meinke DW, Last RL, Conklin PL, Somerville CR. 2001. Arabidopsis cyt1 mutants are deficient in a mannose-1-phosphate guanylyltransferase and point to a requirement of N-linked glycosylation for cellulose biosynthesis. Proc. Natl. Acad. Sci. USA 98: 2262-2267. https://doi.org/10.1073/pnas.051625798
- Lam H, Oh D-C, Cava F, Takacs CN, Clardy J, de Pedro MA, Waldor MK. 2009. D-Amino acids govern stationary phase cell wall remodeling in bacteria. Science 325: 1552-1555. https://doi.org/10.1126/science.1178123
- Olsiewski PJ, Kaczorowski G, Walsh C. 1980. Purification and properties of D-amino acid dehydrogenase, an inducible membrane-bound iron-sulfur flavoenzyme from Escherichia coli B. J. Biol. Chem. 255: 4487-4494.
- Justice SS, Hunstad DA, Harper JR, Duguay AR, Pinkner JS, Bann J, et al. 2005. Periplasmic peptidyl prolyl cis-trans isomerases are not essential for viability, but SurA is required for pilus biogenesis in Escherichia coli. J. Bacteriol. 187: 7680-7686. https://doi.org/10.1128/JB.187.22.7680-7686.2005
- Kuhad RC, Singh S, Singh A. 2011. Phosphate-solubilizing microorganisms, pp. 65-84. In Singh A, Parmar N, Kuhad RC (eds.). Bioaugmentation, Biostimulation and Biocontrol, 1st Ed. Springer-Verlag, Berlin-Heidelberg. Germany.
- Berka TR, Allenza P, Lessie TG. 1984. Hyperinduction of enzymes of the phosphorylative pathway of glucose dissimilation in Pseudomonas cepacia. Curr. Microbiol. 11: 143-148. https://doi.org/10.1007/BF01567339
- Farhat MB, Fourati A, Chouayekh H. 2013. Coexpression of the pyrroloquinoline quinone and glucose dehydrogenase genes from Serratia marcescens CTM 50650 conferred high mineral phosphate-solubilizing ability to Escherichia coli. Appl. Biochem. Biotechnol. 170: 1738-1750. https://doi.org/10.1007/s12010-013-0305-0
- Liu S-T, Lee L, Tai C-Y, Hung C, Chang Y, Wolfram JH, et al. 1992. Cloning of an Erwinia herbicola gene necessary for gluconic acid production and enhanced mineral phosphate solubilization in Escherichia coli HB101: nucleotide sequence and probable involvement in biosynthesis of the coenzyme pyrroloquinoline quinone. J. Bacteriol. 174: 5814-5819. https://doi.org/10.1128/jb.174.18.5814-5819.1992
- Reher M, Bott M, Schonheit P. 2006. Characterization of glycerate kinase (2-phosphoglycerate forming), a key enzyme of the nonphosphorylative Entner-Doudoroff pathway, from the thermoacidophilic euryarchaeon Picrophilus torridus. FEMS Microbiol. Lett. 259: 113-119. https://doi.org/10.1111/j.1574-6968.2006.00264.x
- Tretter L, Adam-Vizi V. 2005. Alpha-ketoglutarate dehydrogenase: a target and generator of oxidative stress. Phil. Trans. R. Soc. B Biol. Sci. 360: 2335-2345. https://doi.org/10.1098/rstb.2005.1764
- Conway T. 1992. The Entner-Doudoroff pathway: history, physiology and molecular biology. FEMS Microbiol. Rev. 103: 1-28. https://doi.org/10.1111/j.1574-6968.1992.tb05822.x
- Basu A, Phale PS. 2006. Inducible uptake and metabolism of glucose by the phosphorylative pathway in Pseudomonas putida CSV86. FEMS Microbiol. Lett. 259: 311-316. https://doi.org/10.1111/j.1574-6968.2006.00285.x
- Elferink MG, Albers SV, Konings WN, Driessen AJ. 2001. Sugar transport in Sulfolobus solfataricus is mediated by two families of binding protein-dependent ABC transporters. Mol. Microbiol. 39: 1494-1503. https://doi.org/10.1046/j.1365-2958.2001.02336.x
- Albers S-V, Elferink MG, Charlebois RL, Sensen CW, Driessen AJ, Konings WN. 1999. Glucose transport in the extremely thermoacidophilic Sulfolobus solfataricus involves a high-affinity membrane-integrated binding protein. J. Bacteriol. 181: 4285-4291.
- Lamarche MG, Wanner BL, Crepin S, Harel J. 2008. The phosphate regulon and bacterial virulence: a regulatory network connecting phosphate homeostasis and pathogenesis. FEMS Microbiol. Rev. 32: 461-473. https://doi.org/10.1111/j.1574-6976.2008.00101.x
- Antelmann H, Scharf C, Hecker M. 2000. Phosphate starvation-inducible proteins of Bacillus subtilis: proteomics and transcriptional analysis. J. Bacteriol. 182: 4478-4490. https://doi.org/10.1128/JB.182.16.4478-4490.2000
- Hsieh Y-J, Wanner BL. 2010. Global regulation by the seven-component Pi signaling system. Curr. Opin. Microbiol. 13: 198-203. https://doi.org/10.1016/j.mib.2010.01.014
- Hulett F, Lee J, Shi L, Sun G, Chesnut R, Sharkova E, et al. 1994. Sequential action of two-component genetic switches regulates the PHO regulon in Bacillus subtilis. J. Bacteriol. 176: 1348-1358. https://doi.org/10.1128/jb.176.5.1348-1358.1994
- Eder S, Shi L, Jensen K, Yamane K, Hulett FM. 1996. A Bacillus subtilis secreted phosphodiesterase/alkaline phosphatase is the product of a Pho regulon gene, phoD. Microbiology 142: 2041-2047. https://doi.org/10.1099/13500872-142-8-2041
- Maddocks SE, Oyston PC. 2008. Structure and function of the LysR-type transcriptional regulator (LTTR) family proteins. Microbiology 154: 3609-3623. https://doi.org/10.1099/mic.0.2008/022772-0
- Heller KJ, Kadner RJ, Gunther K. 1988. Suppression of the btuB451 mutation by mutations in the tonB gene suggests a direct interaction between TonB and TonB-dependent receptor proteins in the outer membrane of Escherichia coli. Gene 64: 147-153. https://doi.org/10.1016/0378-1119(88)90488-X
- Braun V, Mahren S, Ogierman M. 2003. Regulation of the FecI-type ECF sigma factor by transmembrane signalling. Curr. Opin. Microbiol. 6: 173-180. https://doi.org/10.1016/S1369-5274(03)00022-5
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