Polyphosphate Plays a Significant Role in the Maturation of Spores in Myxococcus xanthus.


Journal

Current microbiology
ISSN: 1432-0991
Titre abrégé: Curr Microbiol
Pays: United States
ID NLM: 7808448

Informations de publication

Date de publication:
01 Jul 2024
Historique:
received: 13 03 2024
accepted: 18 06 2024
medline: 2 7 2024
pubmed: 2 7 2024
entrez: 1 7 2024
Statut: epublish

Résumé

Myxococcus xanthus synthesizes polyphosphates (polyPs) with polyphosphate kinase 1 (Ppk1) and degrades short- and long-chain polyPs with the exopolyphosphatases, Ppx1 and Ppx2, respectively. M. xanthus polyP:AMP phosphotransferase (Pap) generates ADP from AMP and polyPs. Pap expression is induced by an elevation in intracellular polyP concentration. M. xanthus synthesized polyPs during the stationary phase; the ppk1 mutant died earlier than the wild-type strain after the stationary phase. In addition, M. xanthus cells cultured in phosphate-starved medium, H

Identifiants

pubmed: 38951187
doi: 10.1007/s00284-024-03778-7
pii: 10.1007/s00284-024-03778-7
doi:

Substances chimiques

Polyphosphates 0
polyphosphate kinase EC 2.7.4.1
Bacterial Proteins 0
Phosphotransferases (Phosphate Group Acceptor) EC 2.7.4.-
exopolyphosphatase EC 3.6.1.11
Acid Anhydride Hydrolases EC 3.6.-
Culture Media 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

248

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Kornberg A (1995) Inorganic polyphosphate: toward making a forgotten polymer unforgettable. J Bacteriol 177:491–496
doi: 10.1128/jb.177.3.491-496.1995 pubmed: 7836277 pmcid: 176618
Zhang H, Ishige K, Kornberg A (2002) A polyphosphate kinase (PPK2) widely conserved in bacteria. Proc Natl Acad Sci USA 99:16678–16683
doi: 10.1073/pnas.262655199 pubmed: 12486232 pmcid: 139203
Hildenbrand JC, Teleki A, Jendrossek D (2020) A universal polyphosphate kinase: PPK2c of Ralstonia eutropha accepts purine and pyrimidine nucleotides including uridine diphosphate. Appl Microbiol Biotechnol 104:6659–6667
doi: 10.1007/s00253-020-10706-9 pubmed: 32500270 pmcid: 7347700
Ishige K, Noguchi T (2001) Polyphosphate:AMP Phosphotransferase and polyphosphate:ADP phosphotransferase activities of Pseudomonas aeruginosa. Biochem Biophys Res Commun 281:821–826
doi: 10.1006/bbrc.2001.4415 pubmed: 11237733
Akiyama M, Crooke E, Kornberg A (1993) An exopolyphosphatase of Escherichia coli. J Biol Chem 268:633–639
doi: 10.1016/S0021-9258(18)54198-3 pubmed: 8380170
Kornberg A (1999) Inorganic polyphosphate: a molecule of many functions. Prog Mol Subcell Biol 23:1–18
doi: 10.1007/978-3-642-58444-2_1 pubmed: 10448669
Rashid MH, Rumbaugh K, Passador L, Davies DG, Hamood AN, Iglewski BH, Kornberg A (2000) Polyphosphate kinase is essential for biofilm development, quorum sensing, and virulence of Pseudomonas aeruginosa. Proc Natl Acad Sci USA 97:9636–9641
doi: 10.1073/pnas.170283397 pubmed: 10931957 pmcid: 16917
Chen W, Palmer RJ, Kuramitsu HK (2002) Role of polyphosphate kinase in biofilm formation by Porphyromonas gingivalis. Infect Immun 70:4708–4715
doi: 10.1128/IAI.70.8.4708-4715.2002 pubmed: 12117989 pmcid: 128176
Reusch RN, Sadoff HL (1988) Putative structure and functions of a poly-β-hydroxybutyrate/calcium polyphosphate channel in bacterial plasma membranes. Proc Natl Acad Sci USA 85:4176–4180
doi: 10.1073/pnas.85.12.4176 pubmed: 2454464 pmcid: 280389
Nomura K, Kato J, Takiguchi N, Ohtake H, Kuroda A (2004) Effects of inorganic polyphosphate on the proteolytic and DNA-binding activities of Lon in Escherichia coli. J Biol Chem 279:34406–34410
doi: 10.1074/jbc.M404725200 pubmed: 15187082
Gray MJ, Wholey W-Y, Wagner NO, Cremers CM, Mueller-Schickert A, Hock NT, Krieger AG, Smith EM, Bender RA, Bardwell JCM, Jakob U (2014) Polyphosphate is a primordial chaperone. Mol Cell 53:689–699
doi: 10.1016/j.molcel.2014.01.012 pubmed: 24560923 pmcid: 3996911
Watson B, Dworkin M (1968) Comparative intermediary metabolism of vegetative cells and microcysts of Myxococcus xanthus. J Bacteriol 96:1456–1473
doi: 10.1128/jb.96.5.1465-1473.1968
Bretscher AP, Kaiser D (1978) Nutrition of Myxococcus xanthus, a fruiting myxobacterium. J Bacteriol 133:763–768
doi: 10.1128/jb.133.2.763-768.1978 pubmed: 415048 pmcid: 222085
Youderian P, Lawes MC, Creighton C, Cook JC, Saier MH (1999) Mutations that confer resistance to 2-deoxyglucose reduce the specific activity of hexokinase from Myxococcus xanthus. J Bacteriol 181:2225–2235
doi: 10.1128/JB.181.7.2225-2235.1999 pubmed: 10094702 pmcid: 93637
Zhang H, Rao NN, Shiba T, Kornberg A (2005) Inorganic polyphosphate in the social life of Myxococcus xanthus: motility, development, and predation. Proc Natl Acad Sci USA 102:13416–13420
doi: 10.1073/pnas.0506520102 pubmed: 16174737 pmcid: 1224657
Kamatani S, Takegawa K, Kimura Y (2018) Catalytic activity profile of polyphosphate kinase 1 from Myxococcus xanthus. Curr Microbiol 75:379–385
doi: 10.1007/s00284-017-1391-y pubmed: 29127456
Kimura Y, Kamatani S (2021) Catalytic activity profile of polyP:AMP phosphotransferase from Myxococcus xanthus. J Biosci Bioeng 131:147–152
doi: 10.1016/j.jbiosc.2020.09.016 pubmed: 33132038
Harita D, Kanie K, Kimura Y (2021) Enzymatic properties of Myxococcus xanthus exopolyphosphatases mxPpx1 and mxPpx2. Biochim Biophys Acta-Proteins Proteom 1869(8):140660
doi: 10.1016/j.bbapap.2021.140660 pubmed: 33857634
Kimura Y, Kamimoto T, Tanaka N (2020) Enzymatic characteristics of a polyphosphate/ATP-NAD kinase, PanK, from Myxococcus xanthus. Curr Microbiol 77:173–178
doi: 10.1007/s00284-019-01810-9 pubmed: 31741028
Harita D, Nishida K, Kimura Y (2023) Synthesis and degradation of polyphosphate in Myxococcus xanthus. FEMS Microbiol Lett 370 fnad007
Livermorea TM, Chubba JR, Saiardia A (2016) Developmental accumulation of inorganic polyphosphate affects germination and energetic metabolism in Dictyostelium discoideum. Proc Natl Acad Sci USA 113:996–1001
doi: 10.1073/pnas.1519440113
Hodgkin J, Kaiser D (1977) Cell-to-cell stimulation of movement in non-motile mutants of Myxococcus. Proc Natl Acad Sci USA 74:2938–2942
doi: 10.1073/pnas.74.7.2938 pubmed: 16592422 pmcid: 431354
Hagan DC, Bretscher AP, Kaiser D (1978) Synergism between morphogenetic mutants of Myxococcus xanthus. Dev Biol 64:284–296
doi: 10.1016/0012-1606(78)90079-9
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
doi: 10.1016/0003-2697(76)90527-3 pubmed: 942051
Kimura Y, Yamamoto H, Kamatani S (2019) Enzymatic characteristics of two adenylate kinases, AdkA and AdkB, from Myxococcus xanthus. J Biochem 165:379–385
doi: 10.1093/jb/mvy112 pubmed: 30535229
Rao NN, Liu S, Kornberg A (1998) Inorganic polyphosphate in Escherichia coli: the phosphate regulon and the stringent response. J Bacteriol 180:2186–2193
doi: 10.1128/JB.180.8.2186-2193.1998 pubmed: 9555903 pmcid: 107147
Shi X, Rao NN, Kornberg A (2002) Inorganic polyphosphate in Bacillus cereus: motility, biofilm formation, and sporulation. Proc Natl Acad Sci USA 101:17061–17065
doi: 10.1073/pnas.0407787101
Atkinson DE (1977) Adenylate control and the adenylate energy charge in cellular energy metabolism and its regulation. Academic Press, New York, pp 85–107
doi: 10.1016/B978-0-12-066150-3.50008-9
Kameda A, Shiba T, Kawazoe Y, Satoh Y, Ihara Y, Munekata M, Ishige K, Noguchi T (2001) A novel ATP regeneration system using polyphosphate-AMP phosphotransferase and polyphosphate kinase. J Biosci Bioeng 91:557–563
doi: 10.1016/S1389-1723(01)80173-0 pubmed: 16233039
Lv H, Zhou Y, Liu B, Guan J, Zhang P, Deng X, Li D, Wanget J (2022) Polyphosphate kinase is required for the processes of virulence and persistence in Acinetobacter baumannii. Microbiol Spectr 10:e01230-e1322
doi: 10.1128/spectrum.01230-22 pubmed: 35867473 pmcid: 9430702
Kimura Y, Yoshioka Y, Toshikuni K (2022) Physiological roles of catalases Cat1 and Cat2 in Myxococcus xanthus. J Microbiol 60:1168–1177
doi: 10.1007/s12275-022-2277-7
Knowles JR (1980) Enzyme-catalyzed phosphoryl transfer reactions. Annu Rev Biochem 49:877–919
doi: 10.1146/annurev.bi.49.070180.004305 pubmed: 6250450
Atkinson DE, Walton GM (1967) Adenosine triphosphate conservation in metabolic regulation. Rat liver citrate cleavage enzyme. J Biol Chem 242:3239–3241
doi: 10.1016/S0021-9258(18)95956-9 pubmed: 6027798
De La Fuente IM, Cortés JM, Valero E, Desroches M, Rodrigues S, Malaina I, Martínez L (2014) On the dynamics of the adenylate energy system: Homeorhesis vs homeostasis. PLoS ONE 9(10):e108676
doi: 10.1371/journal.pone.0108676 pubmed: 25303477 pmcid: 4193753

Auteurs

Daiki Harita (D)

Department of Applied Biological Science, Faculty of Agriculture, Kagawa University, Miki-cho, Kagawa, Japan.

Hiroka Matsukawa (H)

Department of Applied Biological Science, Faculty of Agriculture, Kagawa University, Miki-cho, Kagawa, Japan.

Yoshio Kimura (Y)

Department of Applied Biological Science, Faculty of Agriculture, Kagawa University, Miki-cho, Kagawa, Japan. kimura.yoshio@kagawa-u.ac.jp.

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