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Advances in Phenazines over the Past Decade: Review of Their Pharmacological Activities, Mechanisms of Action, Biosynthetic Pathways and Synthetic Strategies.

Marine drugs

Yan J, Liu W, Cai J, Wang Y, Li D, Hua H, Cao H.
PMID: 34822481
Mar Drugs. 2021 Oct 27;19(11). doi: 10.3390/md19110610.

Phenazines are a large group of nitrogen-containing heterocycles, providing diverse chemical structures and various biological activities. Natural phenazines are mainly isolated from marine and terrestrial microorganisms. So far, more than 100 different natural compounds and over 6000 synthetic derivatives...

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Yan J, Liu W, Cai J, et al. Advances in Phenazines over the Past Decade: Review of Their Pharmacological Activities, Mechanisms of Action, Biosynthetic Pathways and Synthetic Strategies. Mar Drugs. 2021;19(11)doi: 10.3390/md19110610.
Yan, J., Liu, W., Cai, J., Wang, Y., Li, D., Hua, H., & Cao, H. (2021). Advances in Phenazines over the Past Decade: Review of Their Pharmacological Activities, Mechanisms of Action, Biosynthetic Pathways and Synthetic Strategies. Marine drugs, 19(11), . https://doi.org/10.3390/md19110610
Yan, Junjie, et al. "Advances in Phenazines over the Past Decade: Review of Their Pharmacological Activities, Mechanisms of Action, Biosynthetic Pathways and Synthetic Strategies." Marine drugs vol. 19,11 (2021). doi: https://doi.org/10.3390/md19110610
Yan J, Liu W, Cai J, Wang Y, Li D, Hua H, Cao H. Advances in Phenazines over the Past Decade: Review of Their Pharmacological Activities, Mechanisms of Action, Biosynthetic Pathways and Synthetic Strategies. Mar Drugs. 2021 Oct 27;19(11). doi: 10.3390/md19110610. PMID: 34822481; PMCID: PMC8620606.
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Identification and Quantification of Secondary Metabolites by LC-MS from Plant-associated .

Bio-protocol

Shahid I, Rizwan M, Mehnaz S.
PMID: 34179247
Bio Protoc. 2018 Jan 20;8(2):e2702. doi: 10.21769/BioProtoc.2702. eCollection 2018 Jan 20.

Increased antibiotic resistance of plants and human pathogens and continuous use of chemical fertilizers has pushed microbiologists to explore new microbial sources as potential antagonists. In this study, eight strains of

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Shahid I, Rizwan M, Mehnaz S. Identification and Quantification of Secondary Metabolites by LC-MS from Plant-associated . Bio Protoc. 2018;8(2):e2702doi: 10.21769/BioProtoc.2702.
Shahid, I., Rizwan, M., & Mehnaz, S. (2018). Identification and Quantification of Secondary Metabolites by LC-MS from Plant-associated . Bio-protocol, 8(2), e2702. https://doi.org/10.21769/BioProtoc.2702
Shahid, Izzah, et al. "Identification and Quantification of Secondary Metabolites by LC-MS from Plant-associated ." Bio-protocol vol. 8,2 (2018): e2702. doi: https://doi.org/10.21769/BioProtoc.2702
Shahid I, Rizwan M, Mehnaz S. Identification and Quantification of Secondary Metabolites by LC-MS from Plant-associated . Bio Protoc. 2018 Jan 20;8(2):e2702. doi: 10.21769/BioProtoc.2702. eCollection 2018 Jan 20. PMID: 34179247; PMCID: PMC8203958.
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Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE.

Metabolic engineering

Ke J, Zhao Z, Coates CR, Hadjithomas M, Kuftin A, Louie K, Weller D, Thomashow L, Mouncey NJ, Northen TR, Yoshikuni Y.
PMID: 34890798
Metab Eng. 2021 Dec 08;69:188-197. doi: 10.1016/j.ymben.2021.11.012. Epub 2021 Dec 08.

Phenazines (Phzs), a family of chemicals with a phenazine backbone, are secondary metabolites with diverse properties such as antibacterial, anti-fungal, or anticancer activity. The core derivatives of phenazine, phenazine-1-carboxylic acid (PCA) and phenazine-1,6-dicarboxylic acid (PDC), are themselves precursors for...

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Ke J, Zhao Z, Coates CR, et al. Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE. Metab Eng. 2021;69:188-197doi: 10.1016/j.ymben.2021.11.012.
Ke, J., Zhao, Z., Coates, C. R., Hadjithomas, M., Kuftin, A., Louie, K., Weller, D., Thomashow, L., Mouncey, N. J., Northen, T. R., & Yoshikuni, Y. (2021). Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE. Metabolic engineering, 69188-197. https://doi.org/10.1016/j.ymben.2021.11.012
Ke, Jing, et al. "Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE." Metabolic engineering vol. 69 (2021): 188-197. doi: https://doi.org/10.1016/j.ymben.2021.11.012
Ke J, Zhao Z, Coates CR, Hadjithomas M, Kuftin A, Louie K, Weller D, Thomashow L, Mouncey NJ, Northen TR, Yoshikuni Y. Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE. Metab Eng. 2021 Dec 08;69:188-197. doi: 10.1016/j.ymben.2021.11.012. Epub 2021 Dec 08. PMID: 34890798.
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Streptomyces spp. enhance vegetative growth of maize plants under saline stress.

Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]

Nozari RM, Ortolan F, Astarita LV, Santarém ER.
PMID: 33834385
Braz J Microbiol. 2021 Sep;52(3):1371-1383. doi: 10.1007/s42770-021-00480-9. Epub 2021 Apr 09.

Saline stress is one of the abiotic stresses that most compromises the yield of crops and can be mitigated by plant growth-promoting rhizobacteria (PGPR). This work characterized rhizobacteria isolates from the genus Streptomyces as PGPR and evaluated their role...

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Nozari RM, Ortolan F, Astarita LV, et al. Streptomyces spp. enhance vegetative growth of maize plants under saline stress. Braz J Microbiol. 2021;52(3):1371-1383doi: 10.1007/s42770-021-00480-9.
Nozari, R. M., Ortolan, F., Astarita, L. V., & Santarém, E. R. (2021). Streptomyces spp. enhance vegetative growth of maize plants under saline stress. Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 52(3), 1371-1383. https://doi.org/10.1007/s42770-021-00480-9
Nozari, Rafaela Mendonça, et al. "Streptomyces spp. enhance vegetative growth of maize plants under saline stress." Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] vol. 52,3 (2021): 1371-1383. doi: https://doi.org/10.1007/s42770-021-00480-9
Nozari RM, Ortolan F, Astarita LV, Santarém ER. Streptomyces spp. enhance vegetative growth of maize plants under saline stress. Braz J Microbiol. 2021 Sep;52(3):1371-1383. doi: 10.1007/s42770-021-00480-9. Epub 2021 Apr 09. PMID: 33834385; PMCID: PMC8324692.
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Transition Metal-Free Heteroarylation of Quinoxaline: Construction of Heteroaryl-Fused Phenazines by Oxidative Coupling.

The Journal of organic chemistry

Uçar S, Daştan A.
PMID: 33185428
J Org Chem. 2020 Dec 04;85(23):15502-15513. doi: 10.1021/acs.joc.0c02252. Epub 2020 Nov 13.

A concise method for the construction of heteroaryl-fused phenazines was developed via PIFA-BF

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Uçar S, Daştan A. Transition Metal-Free Heteroarylation of Quinoxaline: Construction of Heteroaryl-Fused Phenazines by Oxidative Coupling. J Org Chem. 2020;85(23):15502-15513doi: 10.1021/acs.joc.0c02252.
Uçar, S., & Daştan, A. (2020). Transition Metal-Free Heteroarylation of Quinoxaline: Construction of Heteroaryl-Fused Phenazines by Oxidative Coupling. The Journal of organic chemistry, 85(23), 15502-15513. https://doi.org/10.1021/acs.joc.0c02252
Uçar, Sefa, and Daştan, Arif. "Transition Metal-Free Heteroarylation of Quinoxaline: Construction of Heteroaryl-Fused Phenazines by Oxidative Coupling." The Journal of organic chemistry vol. 85,23 (2020): 15502-15513. doi: https://doi.org/10.1021/acs.joc.0c02252
Uçar S, Daştan A. Transition Metal-Free Heteroarylation of Quinoxaline: Construction of Heteroaryl-Fused Phenazines by Oxidative Coupling. J Org Chem. 2020 Dec 04;85(23):15502-15513. doi: 10.1021/acs.joc.0c02252. Epub 2020 Nov 13. PMID: 33185428.
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Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE.

Metabolic engineering

Ke J, Zhao Z, Coates CR, Hadjithomas M, Kuftin A, Louie K, Weller D, Thomashow L, Mouncey NJ, Northen TR, Yoshikuni Y.
PMID: 34890798
Metab Eng. 2021 Dec 08;69:188-197. doi: 10.1016/j.ymben.2021.11.012. Epub 2021 Dec 08.

Phenazines (Phzs), a family of chemicals with a phenazine backbone, are secondary metabolites with diverse properties such as antibacterial, anti-fungal, or anticancer activity. The core derivatives of phenazine, phenazine-1-carboxylic acid (PCA) and phenazine-1,6-dicarboxylic acid (PDC), are themselves precursors for...

Cite
Ke J, Zhao Z, Coates CR, et al. Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE. Metab Eng. 2021;69:188-197doi: 10.1016/j.ymben.2021.11.012.
Ke, J., Zhao, Z., Coates, C. R., Hadjithomas, M., Kuftin, A., Louie, K., Weller, D., Thomashow, L., Mouncey, N. J., Northen, T. R., & Yoshikuni, Y. (2021). Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE. Metabolic engineering, 69188-197. https://doi.org/10.1016/j.ymben.2021.11.012
Ke, Jing, et al. "Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE." Metabolic engineering vol. 69 (2021): 188-197. doi: https://doi.org/10.1016/j.ymben.2021.11.012
Ke J, Zhao Z, Coates CR, Hadjithomas M, Kuftin A, Louie K, Weller D, Thomashow L, Mouncey NJ, Northen TR, Yoshikuni Y. Development of platforms for functional characterization and production of phenazines using a multi-chassis approach via CRAGE. Metab Eng. 2021 Dec 08;69:188-197. doi: 10.1016/j.ymben.2021.11.012. Epub 2021 Dec 08. PMID: 34890798.
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Fluorescent redox-dependent labeling of lipid droplets in cultured cells by reduced phenazine methosulfate.

Heliyon

Stockert JC, Carou MC, Casas AG, García Vior MC, Ezquerra Riega SD, Blanco MM, Espada J, Blázquez-Castro A, Horobin RW, Lombardo DM.
PMID: 32566788
Heliyon. 2020 Jun 13;6(6):e04182. doi: 10.1016/j.heliyon.2020.e04182. eCollection 2020 Jun.

Natural and synthetic phenazines are widely used in biomedical sciences. In dehydrogenase histochemistry, phenazine methosulfate (PMS) is applied as a redox reagent for coupling reduced coenzymes to the reduction of tetrazolium salts into colored formazans. PMS is also currently...

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Stockert JC, Carou MC, Casas AG, et al. Fluorescent redox-dependent labeling of lipid droplets in cultured cells by reduced phenazine methosulfate. Heliyon. 2020;6(6):e04182doi: 10.1016/j.heliyon.2020.e04182.
Stockert, J. C., Carou, M. C., Casas, A. G., García Vior, M. C., Ezquerra Riega, S. D., Blanco, M. M., Espada, J., Blázquez-Castro, A., Horobin, R. W., & Lombardo, D. M. (2020). Fluorescent redox-dependent labeling of lipid droplets in cultured cells by reduced phenazine methosulfate. Heliyon, 6(6), e04182. https://doi.org/10.1016/j.heliyon.2020.e04182
Stockert, Juan C, et al. "Fluorescent redox-dependent labeling of lipid droplets in cultured cells by reduced phenazine methosulfate." Heliyon vol. 6,6 (2020): e04182. doi: https://doi.org/10.1016/j.heliyon.2020.e04182
Stockert JC, Carou MC, Casas AG, García Vior MC, Ezquerra Riega SD, Blanco MM, Espada J, Blázquez-Castro A, Horobin RW, Lombardo DM. Fluorescent redox-dependent labeling of lipid droplets in cultured cells by reduced phenazine methosulfate. Heliyon. 2020 Jun 13;6(6):e04182. doi: 10.1016/j.heliyon.2020.e04182. eCollection 2020 Jun. PMID: 32566788; PMCID: PMC7298651.
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Characteristics of biological control and mechanisms of Pseudomonas chlororaphis zm-1 against peanut stem rot.

BMC microbiology

Liu F, Yang S, Xu F, Zhang Z, Lu Y, Zhang J, Wang G.
PMID: 34986788
BMC Microbiol. 2022 Jan 05;22(1):9. doi: 10.1186/s12866-021-02420-x.

BACKGROUND: Peanut stem rot is a serious plant disease that causes great economic losses. At present, there are no effective measures to prevent or control the occurrence of this plant disease. Biological control is one of the most promising...

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Liu F, Yang S, Xu F, et al. Characteristics of biological control and mechanisms of Pseudomonas chlororaphis zm-1 against peanut stem rot. BMC Microbiol. 2022;22(1):9doi: 10.1186/s12866-021-02420-x.
Liu, F., Yang, S., Xu, F., Zhang, Z., Lu, Y., Zhang, J., & Wang, G. (2022). Characteristics of biological control and mechanisms of Pseudomonas chlororaphis zm-1 against peanut stem rot. BMC microbiology, 22(1), 9. https://doi.org/10.1186/s12866-021-02420-x
Liu, Fengying, et al. "Characteristics of biological control and mechanisms of Pseudomonas chlororaphis zm-1 against peanut stem rot." BMC microbiology vol. 22,1 (2022): 9. doi: https://doi.org/10.1186/s12866-021-02420-x
Liu F, Yang S, Xu F, Zhang Z, Lu Y, Zhang J, Wang G. Characteristics of biological control and mechanisms of Pseudomonas chlororaphis zm-1 against peanut stem rot. BMC Microbiol. 2022 Jan 05;22(1):9. doi: 10.1186/s12866-021-02420-x. PMID: 34986788.
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Soil bacteria protect fungi from phenazines by acting as toxin sponges.

Current biology : CB

Dahlstrom KM, Newman DK.
PMID: 34813731
Curr Biol. 2021 Nov 17; doi: 10.1016/j.cub.2021.11.002. Epub 2021 Nov 17.

Many environmentally and clinically important fungi are sensitive to toxic, bacterially produced, redox-active molecules called phenazines. Despite being vulnerable to phenazine assault, fungi inhabit microbial communities that contain phenazine producers. Because many fungi cannot withstand phenazine challenge but some...

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Dahlstrom KM, Newman DK. Soil bacteria protect fungi from phenazines by acting as toxin sponges. Curr Biol. 2021;doi: 10.1016/j.cub.2021.11.002.
Dahlstrom, K. M., & Newman, D. K. (2021). Soil bacteria protect fungi from phenazines by acting as toxin sponges. Current biology : CB, . https://doi.org/10.1016/j.cub.2021.11.002
Dahlstrom, Kurt M, and Newman, Dianne K. "Soil bacteria protect fungi from phenazines by acting as toxin sponges." Current biology : CB vol. (2021). doi: https://doi.org/10.1016/j.cub.2021.11.002
Dahlstrom KM, Newman DK. Soil bacteria protect fungi from phenazines by acting as toxin sponges. Curr Biol. 2021 Nov 17; doi: 10.1016/j.cub.2021.11.002. Epub 2021 Nov 17. PMID: 34813731.
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[No title available]

Current research in microbial sciences

Sah S, Krishnani S, Singh R.
PMID: 34917993
Curr Res Microb Sci. 2021 Nov 24;2:100084. doi: 10.1016/j.crmicr.2021.100084. eCollection 2021 Dec.

Numerous microbial communities show synergistic and antagonistic interactions among themselves, resulting in benefit and harm to either or both the associated members. The association holds accountability for nutrients recycling and energy drift, resulting in the availability of macronutrients unavailable...

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Sah S, Krishnani S, Singh R. . Curr Res Microb Sci. 2021;2:100084doi: 10.1016/j.crmicr.2021.100084.
Sah, S., Krishnani, S., & Singh, R. (2021). . Current research in microbial sciences, 2100084. https://doi.org/10.1016/j.crmicr.2021.100084
Sah, Stuti, et al. "." Current research in microbial sciences vol. 2 (2021): 100084. doi: https://doi.org/10.1016/j.crmicr.2021.100084
Sah S, Krishnani S, Singh R. . Curr Res Microb Sci. 2021 Nov 24;2:100084. doi: 10.1016/j.crmicr.2021.100084. eCollection 2021 Dec. PMID: 34917993; PMCID: PMC8645841.
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Super electron donor-mediated reductive transformation of nitrobenzenes: a novel strategy to synthesize azobenzenes and phenazines.

Organic & biomolecular chemistry

Nozawa-Kumada K, Abe E, Ito S, Shigeno M, Kondo Y.
PMID: 29634065
Org Biomol Chem. 2018 May 02;16(17):3095-3098. doi: 10.1039/c8ob00271a.

The transformation of nitrobenzenes into azobenzenes by pyridine-derived super electron donor 2 is described. This method provides an efficient synthesis of azobenzenes because of not requiring the use of expensive transition-metals, toxic or flammable reagents, or harsh conditions. Moreover,...

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Nozawa-Kumada K, Abe E, Ito S, et al. Super electron donor-mediated reductive transformation of nitrobenzenes: a novel strategy to synthesize azobenzenes and phenazines. Org Biomol Chem. 2018;16(17):3095-3098doi: 10.1039/c8ob00271a.
Nozawa-Kumada, K., Abe, E., Ito, S., Shigeno, M., & Kondo, Y. (2018). Super electron donor-mediated reductive transformation of nitrobenzenes: a novel strategy to synthesize azobenzenes and phenazines. Organic & biomolecular chemistry, 16(17), 3095-3098. https://doi.org/10.1039/c8ob00271a
Nozawa-Kumada, Kanako, et al. "Super electron donor-mediated reductive transformation of nitrobenzenes: a novel strategy to synthesize azobenzenes and phenazines." Organic & biomolecular chemistry vol. 16,17 (2018): 3095-3098. doi: https://doi.org/10.1039/c8ob00271a
Nozawa-Kumada K, Abe E, Ito S, Shigeno M, Kondo Y. Super electron donor-mediated reductive transformation of nitrobenzenes: a novel strategy to synthesize azobenzenes and phenazines. Org Biomol Chem. 2018 May 02;16(17):3095-3098. doi: 10.1039/c8ob00271a. PMID: 29634065.
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Snapshotting the Excited-State Planarization of Chemically Locked N,N'-Disubstituted Dihydrodibenzo[a,c]phenazines.

Journal of the American Chemical Society

Chen W, Chen CL, Zhang Z, Chen YA, Chao WC, Su J, Tian H, Chou PT.
PMID: 28072523
J Am Chem Soc. 2017 Feb 01;139(4):1636-1644. doi: 10.1021/jacs.6b11789. Epub 2017 Jan 24.

For deeper understanding of the coupling of electronic processes with conformational motions, we exploit a tailored strategy to harness the excited-state planarization of N,N'-disubstituted dihydrodibenzo[a,c]phenazines by halting the structural evolution via a macrocyclization process. In this new approach, 9,14-diphenyl-9,14-dihydrodibenzo[a,c]phenazine...

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Chen W, Chen CL, Zhang Z, et al. Snapshotting the Excited-State Planarization of Chemically Locked N,N'-Disubstituted Dihydrodibenzo[a,c]phenazines. J Am Chem Soc. 2017;139(4):1636-1644doi: 10.1021/jacs.6b11789.
Chen, W., Chen, C. L., Zhang, Z., Chen, Y. A., Chao, W. C., Su, J., Tian, H., & Chou, P. T. (2017). Snapshotting the Excited-State Planarization of Chemically Locked N,N'-Disubstituted Dihydrodibenzo[a,c]phenazines. Journal of the American Chemical Society, 139(4), 1636-1644. https://doi.org/10.1021/jacs.6b11789
Chen, Wei, et al. "Snapshotting the Excited-State Planarization of Chemically Locked N,N'-Disubstituted Dihydrodibenzo[a,c]phenazines." Journal of the American Chemical Society vol. 139,4 (2017): 1636-1644. doi: https://doi.org/10.1021/jacs.6b11789
Chen W, Chen CL, Zhang Z, Chen YA, Chao WC, Su J, Tian H, Chou PT. Snapshotting the Excited-State Planarization of Chemically Locked N,N'-Disubstituted Dihydrodibenzo[a,c]phenazines. J Am Chem Soc. 2017 Feb 01;139(4):1636-1644. doi: 10.1021/jacs.6b11789. Epub 2017 Jan 24. PMID: 28072523.
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Showing 13 to 24 of 112 entries