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Characterization of lipopolysaccharides from Escherichia coli K-12 mutants

k-12

[No authors listed]
GSID: BgwnbFeLXd4J
HG Boman, DA Monner - Journal of Bacteriology, 1975 - Am Soc Microbiol

Chemical analyses of the carbohydrate composition of lipopolysaccharides (LPS) from a number of LPS mutants were used to propose a schematic composition for the LPS from Escherichia coli K-12. The formula contains four regions: the first consists of lipid...

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Boman, H. G., & Monner, D. A. (1975). Characterization of lipopolysaccharides from Escherichia coli K-12 mutants. Journal of Bacteriology, 121(2), 455-464.
Boman, HANS G., and DAVID A. Monner. "Characterization of lipopolysaccharides from Escherichia coli K-12 mutants." Journal of Bacteriology 121.2 (1975): 455-464.
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Escherichia coli K-12 suppressor-free mutants lacking early glycosyltransferases and late acyltransferases: minimal lipopolysaccharide structure and …

k-12

Klein G.
GSID: bjNGyGxhYykJ
G Klein, B Lindner, W Brabetz, H Brade… - Journal of biological …, 2009 - ASBMB

… coli K-12, a bisphosphorylated lipid A precursor molecule with two amide and two ester-bound (R)-3-hydroxymyristate residues (lipid IV A ) is synthesized from … coli K-12, which catalyze the latter enzyme reactions using acyl carrier protein-activated fatty acids...

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Klein, G., Lindner, B., Brabetz, W., Brade, H., & Raina, S. (2009). Escherichia coli K-12 suppressor-free mutants lacking early glycosyltransferases and late acyltransferases: minimal lipopolysaccharide structure and induction of envelope stress response. Journal of biological chemistry, 284(23), 15369-15389.
Klein, Gracjana, et al. "Escherichia coli K-12 suppressor-free mutants lacking early glycosyltransferases and late acyltransferases: minimal lipopolysaccharide structure and induction of envelope stress response." Journal of biological chemistry 284.23 (2009): 15369-15389.
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Distinct Effects of Monophosphoryl Lipid A, Oligodeoxynucleotide CpG, and Combination Adjuvants on Modulating Innate and Adaptive Immune Responses to Influenza Vaccination.

Immune network

Ko EJ, Lee YT, Lee Y, Kim KH, Kang SM.
PMID: 29093654
Immune Netw. 2017 Oct;17(5):326-342. doi: 10.4110/in.2017.17.5.326. Epub 2017 Oct 19.

Monophosphoryl lipid A (MPL) and oligodeoxynucleotide CpG are toll-like receptor (TLR) 4 and 9 agonist, respectively. Here, we investigated the effects of MPL, CpG, and combination adjuvants on stimulating

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Ko EJ, Lee YT, Lee Y, et al. Distinct Effects of Monophosphoryl Lipid A, Oligodeoxynucleotide CpG, and Combination Adjuvants on Modulating Innate and Adaptive Immune Responses to Influenza Vaccination. Immune Netw. 2017;17(5):326-342doi: 10.4110/in.2017.17.5.326.
Ko, E. J., Lee, Y. T., Lee, Y., Kim, K. H., & Kang, S. M. (2017). Distinct Effects of Monophosphoryl Lipid A, Oligodeoxynucleotide CpG, and Combination Adjuvants on Modulating Innate and Adaptive Immune Responses to Influenza Vaccination. Immune network, 17(5), 326-342. https://doi.org/10.4110/in.2017.17.5.326
Ko, Eun-Ju, et al. "Distinct Effects of Monophosphoryl Lipid A, Oligodeoxynucleotide CpG, and Combination Adjuvants on Modulating Innate and Adaptive Immune Responses to Influenza Vaccination." Immune network vol. 17,5 (2017): 326-342. doi: https://doi.org/10.4110/in.2017.17.5.326
Ko EJ, Lee YT, Lee Y, Kim KH, Kang SM. Distinct Effects of Monophosphoryl Lipid A, Oligodeoxynucleotide CpG, and Combination Adjuvants on Modulating Innate and Adaptive Immune Responses to Influenza Vaccination. Immune Netw. 2017 Oct;17(5):326-342. doi: 10.4110/in.2017.17.5.326. Epub 2017 Oct 19. PMID: 29093654; PMCID: PMC5662782.
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Mechanisms of polymyxin resistance: acquired and intrinsic resistance in bacteria.

Frontiers in microbiology

Olaitan AO, Morand S, Rolain JM.
PMID: 25505462
Front Microbiol. 2014 Nov 26;5:643. doi: 10.3389/fmicb.2014.00643. eCollection 2014.

Polymyxins are polycationic antimicrobial peptides that are currently the last-resort antibiotics for the treatment of multidrug-resistant, Gram-negative bacterial infections. The reintroduction of polymyxins for antimicrobial therapy has been followed by an increase in reports of resistance among Gram-negative bacteria....

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Olaitan AO, Morand S, Rolain JM. Mechanisms of polymyxin resistance: acquired and intrinsic resistance in bacteria. Front Microbiol. 2014;5:643doi: 10.3389/fmicb.2014.00643.
Olaitan, A. O., Morand, S., & Rolain, J. M. (2014). Mechanisms of polymyxin resistance: acquired and intrinsic resistance in bacteria. Frontiers in microbiology, 5643. https://doi.org/10.3389/fmicb.2014.00643
Olaitan, Abiola O, et al. "Mechanisms of polymyxin resistance: acquired and intrinsic resistance in bacteria." Frontiers in microbiology vol. 5 (2014): 643. doi: https://doi.org/10.3389/fmicb.2014.00643
Olaitan AO, Morand S, Rolain JM. Mechanisms of polymyxin resistance: acquired and intrinsic resistance in bacteria. Front Microbiol. 2014 Nov 26;5:643. doi: 10.3389/fmicb.2014.00643. eCollection 2014. PMID: 25505462; PMCID: PMC4244539.
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The Effect of Temperature, Cations, and Number of Acyl Chains on the Lamellar to Non-Lamellar Transition in Lipid-A Membranes: A Microscopic View.

Journal of chemical theory and computation

Pontes FJ, Rusu VH, Soares TA, Lins RD.
PMID: 26593024
J Chem Theory Comput. 2012 Oct 09;8(10):3830-8. doi: 10.1021/ct300084v. Epub 2012 Jun 05.

Lipopolysaccharides (LPS) are the main constituent of the outer bacterial membrane of Gram-negative bacteria. Lipid-A is the structural region of LPS that interacts with the innate immune system and induces inflammatory responses. It is formed by a phosphorylated β-d-glucosaminyl-(1→6)-α-N-glucosamine...

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Pontes FJ, Rusu VH, Soares TA, et al. The Effect of Temperature, Cations, and Number of Acyl Chains on the Lamellar to Non-Lamellar Transition in Lipid-A Membranes: A Microscopic View. J Chem Theory Comput. 2012;8(10):3830-8doi: 10.1021/ct300084v.
Pontes, F. J., Rusu, V. H., Soares, T. A., & Lins, R. D. (2012). The Effect of Temperature, Cations, and Number of Acyl Chains on the Lamellar to Non-Lamellar Transition in Lipid-A Membranes: A Microscopic View. Journal of chemical theory and computation, 8(10), 3830-8. https://doi.org/10.1021/ct300084v
Pontes, Frederico J S, et al. "The Effect of Temperature, Cations, and Number of Acyl Chains on the Lamellar to Non-Lamellar Transition in Lipid-A Membranes: A Microscopic View." Journal of chemical theory and computation vol. 8,10 (2012): 3830-8. doi: https://doi.org/10.1021/ct300084v
Pontes FJ, Rusu VH, Soares TA, Lins RD. The Effect of Temperature, Cations, and Number of Acyl Chains on the Lamellar to Non-Lamellar Transition in Lipid-A Membranes: A Microscopic View. J Chem Theory Comput. 2012 Oct 09;8(10):3830-8. doi: 10.1021/ct300084v. Epub 2012 Jun 05. PMID: 26593024.
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Hydroxytyrosol and potential uses in cardiovascular diseases, cancer, and AIDS.

Frontiers in nutrition

Vilaplana-Pérez C, Auñón D, García-Flores LA, Gil-Izquierdo A.
PMID: 25988120
Front Nutr. 2014 Oct 27;1:18. doi: 10.3389/fnut.2014.00018. eCollection 2014.

Hydroxytyrosol is one of the main phenolic components of olive oil. It is present in the fruit and leaf of the olive (Olea europaea L.). During the past decades, it has been well documented that this phenolic compound has...

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Vilaplana-Pérez C, Auñón D, García-Flores LA, et al. Hydroxytyrosol and potential uses in cardiovascular diseases, cancer, and AIDS. Front Nutr. 2014;1:18doi: 10.3389/fnut.2014.00018.
Vilaplana-Pérez, C., Auñón, D., García-Flores, L. A., & Gil-Izquierdo, A. (2014). Hydroxytyrosol and potential uses in cardiovascular diseases, cancer, and AIDS. Frontiers in nutrition, 118. https://doi.org/10.3389/fnut.2014.00018
Vilaplana-Pérez, Cristina, et al. "Hydroxytyrosol and potential uses in cardiovascular diseases, cancer, and AIDS." Frontiers in nutrition vol. 1 (2014): 18. doi: https://doi.org/10.3389/fnut.2014.00018
Vilaplana-Pérez C, Auñón D, García-Flores LA, Gil-Izquierdo A. Hydroxytyrosol and potential uses in cardiovascular diseases, cancer, and AIDS. Front Nutr. 2014 Oct 27;1:18. doi: 10.3389/fnut.2014.00018. eCollection 2014. PMID: 25988120; PMCID: PMC4428486.
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The Very Long Chain Fatty Acid (C.

Frontiers in microbiology

Busset N, Di Lorenzo F, Palmigiano A, Sturiale L, Gressent F, Fardoux J, Gully D, Chaintreuil C, Molinaro A, Silipo A, Giraud E.
PMID: 28983292
Front Microbiol. 2017 Sep 21;8:1821. doi: 10.3389/fmicb.2017.01821. eCollection 2017.

In rhizobium strains, the lipid A is modified by the addition of a very long-chain fatty acid (VLCFA) shown to play an important role in rigidification of the outer membrane, thereby facilitating their dual life cycle, outside and inside...

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Busset N, Di Lorenzo F, Palmigiano A, et al. The Very Long Chain Fatty Acid (C. Front Microbiol. 2017;8:1821doi: 10.3389/fmicb.2017.01821.
Busset, N., Di Lorenzo, F., Palmigiano, A., Sturiale, L., Gressent, F., Fardoux, J., Gully, D., Chaintreuil, C., Molinaro, A., Silipo, A., & Giraud, E. (2017). The Very Long Chain Fatty Acid (C. Frontiers in microbiology, 81821. https://doi.org/10.3389/fmicb.2017.01821
Busset, Nicolas, et al. "The Very Long Chain Fatty Acid (C." Frontiers in microbiology vol. 8 (2017): 1821. doi: https://doi.org/10.3389/fmicb.2017.01821
Busset N, Di Lorenzo F, Palmigiano A, Sturiale L, Gressent F, Fardoux J, Gully D, Chaintreuil C, Molinaro A, Silipo A, Giraud E. The Very Long Chain Fatty Acid (C. Front Microbiol. 2017 Sep 21;8:1821. doi: 10.3389/fmicb.2017.01821. eCollection 2017. PMID: 28983292; PMCID: PMC5613085.
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The composition of the global and feature specific cyanobacterial core-genomes.

Frontiers in microbiology

Simm S, Keller M, Selymesi M, Schleiff E.
PMID: 25852675
Front Microbiol. 2015 Mar 19;6:219. doi: 10.3389/fmicb.2015.00219. eCollection 2015.

Cyanobacteria are photosynthetic prokaryotes important for many ecosystems with a high potential for biotechnological usage e.g., in the production of bioactive molecules. Either asks for a deep understanding of the functionality of cyanobacteria and their interaction with the environment....

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Simm S, Keller M, Selymesi M, et al. The composition of the global and feature specific cyanobacterial core-genomes. Front Microbiol. 2015;6:219doi: 10.3389/fmicb.2015.00219.
Simm, S., Keller, M., Selymesi, M., & Schleiff, E. (2015). The composition of the global and feature specific cyanobacterial core-genomes. Frontiers in microbiology, 6219. https://doi.org/10.3389/fmicb.2015.00219
Simm, Stefan, et al. "The composition of the global and feature specific cyanobacterial core-genomes." Frontiers in microbiology vol. 6 (2015): 219. doi: https://doi.org/10.3389/fmicb.2015.00219
Simm S, Keller M, Selymesi M, Schleiff E. The composition of the global and feature specific cyanobacterial core-genomes. Front Microbiol. 2015 Mar 19;6:219. doi: 10.3389/fmicb.2015.00219. eCollection 2015. PMID: 25852675; PMCID: PMC4365693.
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Monophosphoryl Lipid A: A Novel Agent for Inducing Pharmacologic Myocardial Preconditioning.

Journal of thrombosis and thrombolysis

Elliott GT.
PMID: 10613986
J Thromb Thrombolysis. 1996;3(3):225-237. doi: 10.1007/BF00181665.

Myocardial tissue appears to possess an endogenous protective mechanism whereby brief ischemic periods precondition cells to better withstand both reversible and irreversible injury associated with prolonged subsequent ischemic events. Protection develops within minutes of transient ischemia, dissipates within 1-2...

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Elliott GT. Monophosphoryl Lipid A: A Novel Agent for Inducing Pharmacologic Myocardial Preconditioning. J Thromb Thrombolysis. 1996;3(3):225-237doi: 10.1007/BF00181665.
Elliott, G. T. (1996). Monophosphoryl Lipid A: A Novel Agent for Inducing Pharmacologic Myocardial Preconditioning. Journal of thrombosis and thrombolysis, 3(3), 225-237. https://doi.org/10.1007/BF00181665
Elliott. "Monophosphoryl Lipid A: A Novel Agent for Inducing Pharmacologic Myocardial Preconditioning." Journal of thrombosis and thrombolysis vol. 3,3 (1996): 225-237. doi: https://doi.org/10.1007/BF00181665
Elliott GT. Monophosphoryl Lipid A: A Novel Agent for Inducing Pharmacologic Myocardial Preconditioning. J Thromb Thrombolysis. 1996;3(3):225-237. doi: 10.1007/BF00181665. PMID: 10613986.
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Signaling pathway of cardioprotection induced by monophosphoryl lipid A in rabbit myocardium.

Pathophysiology : the official journal of the International Society for Pathophysiology

Xiuhua L, Xudong W, Yue H, Chaoshu T, Jingyi S.
PMID: 12039651
Pathophysiology. 2002 Jun;8(3):193-196. doi: 10.1016/s0928-4680(02)00005-6.

OBJECTIVE: To investigate the effect of monophosphoryl lipid A (MLA) on ischemia/reperfusion (I/R) injury in rabbit heart and its signal transduction pathway. METHODS: Eighteen rabbits were randomly assigned to three groups: (1) MLA-group: Six rabbits received injection of MLA...

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Xiuhua L, Xudong W, Yue H, et al. Signaling pathway of cardioprotection induced by monophosphoryl lipid A in rabbit myocardium. Pathophysiology. 2002;8(3):193-196doi: 10.1016/s0928-4680(02)00005-6.
Xiuhua, L., Xudong, W., Yue, H., Chaoshu, T., & Jingyi, S. (2002). Signaling pathway of cardioprotection induced by monophosphoryl lipid A in rabbit myocardium. Pathophysiology : the official journal of the International Society for Pathophysiology, 8(3), 193-196. https://doi.org/10.1016/s0928-4680(02)00005-6
Xiuhua, Liu, et al. "Signaling pathway of cardioprotection induced by monophosphoryl lipid A in rabbit myocardium." Pathophysiology : the official journal of the International Society for Pathophysiology vol. 8,3 (2002): 193-196. doi: https://doi.org/10.1016/s0928-4680(02)00005-6
Xiuhua L, Xudong W, Yue H, Chaoshu T, Jingyi S. Signaling pathway of cardioprotection induced by monophosphoryl lipid A in rabbit myocardium. Pathophysiology. 2002 Jun;8(3):193-196. doi: 10.1016/s0928-4680(02)00005-6. PMID: 12039651.
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Double pi(0) Photoproduction on the Proton at GRAAL.

Physical review letters

Assafiri Y, Bartalini O, Bellini V, Bocquet JP, Bouchigny S, Capogni M, Castoldi M, D'Angelo A, Didelez JP, Di Salvo R, Fantini A, Fichen L, Gervino G, Ghio F, Girolami B, Giusa A, Guidal M, Hourany E, Kouznetsov V, Kunne R, Laget JM, Lapik A, Sandri PL, Lleres A, Moricciani D, Nedorezov V, Rebreyend D, Randieri C, Renard F, Rudnev N, Schaerf C, Sperduto M, Sutera M, Turinge A, Zucchiatti A.
PMID: 12857308
Phys Rev Lett. 2003 Jun 06;90(22):222001. doi: 10.1103/PhysRevLett.90.222001. Epub 2003 Jun 03.

The double pi(0) photoproduction off the proton has been measured in the beam energy range of 0.65-1.5 GeV. The total and differential cross sections and the Sigma beam asymmetry were extracted. The total cross section measured for the first...

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Assafiri Y, Bartalini O, Bellini V, et al. Double pi(0) Photoproduction on the Proton at GRAAL. Phys Rev Lett. 2003;90(22):222001doi: 10.1103/PhysRevLett.90.222001.
Assafiri, Y., Bartalini, O., Bellini, V., Bocquet, J. P., Bouchigny, S., Capogni, M., Castoldi, M., D'Angelo, A., Didelez, J. P., Di Salvo, R., Fantini, A., Fichen, L., Gervino, G., Ghio, F., Girolami, B., Giusa, A., Guidal, M., Hourany, E., Kouznetsov, V., Kunne, R., Laget, J. M., Lapik, A., Sandri, P. L., Lleres, A., Moricciani, D., Nedorezov, V., Rebreyend, D., Randieri, C., Renard, F., Rudnev, N., Schaerf, C., Sperduto, M., Sutera, M., Turinge, A., & Zucchiatti, A. (2003). Double pi(0) Photoproduction on the Proton at GRAAL. Physical review letters, 90(22), 222001. https://doi.org/10.1103/PhysRevLett.90.222001
Assafiri, Y, et al. "Double pi(0) Photoproduction on the Proton at GRAAL." Physical review letters vol. 90,22 (2003): 222001. doi: https://doi.org/10.1103/PhysRevLett.90.222001
Assafiri Y, Bartalini O, Bellini V, Bocquet JP, Bouchigny S, Capogni M, Castoldi M, D'Angelo A, Didelez JP, Di Salvo R, Fantini A, Fichen L, Gervino G, Ghio F, Girolami B, Giusa A, Guidal M, Hourany E, Kouznetsov V, Kunne R, Laget JM, Lapik A, Sandri PL, Lleres A, Moricciani D, Nedorezov V, Rebreyend D, Randieri C, Renard F, Rudnev N, Schaerf C, Sperduto M, Sutera M, Turinge A, Zucchiatti A. Double pi(0) Photoproduction on the Proton at GRAAL. Phys Rev Lett. 2003 Jun 06;90(22):222001. doi: 10.1103/PhysRevLett.90.222001. Epub 2003 Jun 03. PMID: 12857308.
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Stereoselective preparation of E vinyl zirconium derivatives from E or Z enol ethers.

The Journal of organic chemistry

Liard A, Marek I.
PMID: 11031055
J Org Chem. 2000 Oct 20;65(21):7218-20. doi: 10.1021/jo005561n.

No abstract available.

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Liard A, Marek I. Stereoselective preparation of E vinyl zirconium derivatives from E or Z enol ethers. J Org Chem. 2000;65(21):7218-20doi: 10.1021/jo005561n.
Liard, A., & Marek, I. (2000). Stereoselective preparation of E vinyl zirconium derivatives from E or Z enol ethers. The Journal of organic chemistry, 65(21), 7218-20. https://doi.org/10.1021/jo005561n
Liard, and Marek. "Stereoselective preparation of E vinyl zirconium derivatives from E or Z enol ethers." The Journal of organic chemistry vol. 65,21 (2000): 7218-20. doi: https://doi.org/10.1021/jo005561n
Liard A, Marek I. Stereoselective preparation of E vinyl zirconium derivatives from E or Z enol ethers. J Org Chem. 2000 Oct 20;65(21):7218-20. doi: 10.1021/jo005561n. PMID: 11031055.
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Showing 1 to 12 of 582 entries