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Journal articles on the topic 'Pseudomycena'

Author: Grafiati
Published: 29 July 2024
Last updated: 30 July 2024

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1

di Giorgio, Domenico, Lorenzo Camoni, Camilla Marchiafava, and Alessandro Ballio. "Mechanism of Action of Pseudomycins." Giornale botanico italiano 129, no. 4 (January 1995): 1056–57. http://dx.doi.org/10.1080/11263509509440933.

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2

Rodriguez, Michael J., Matthew Belvo, Robert Morris, Douglas J. Zeckner, William L. Current, Roberta K. Sachs, and Mark J. Zweifel. "The synthesis of pseudomycin C′ via a novel acid promoted side-chain deacylation of pseudomycin A." Bioorganic & Medicinal Chemistry Letters 11, no. 2 (January 2001): 161–64. http://dx.doi.org/10.1016/s0960-894x(00)00613-2.

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3

Rodriguez, Michael J., Matthew Belvo, Robert Morris, Douglas J. Zeckner, William L. Current, Roberta K. Sachs, and Mark J. Zweifel. "ChemInform Abstract: Synthesis of Pseudomycin C′ (Ib) via a Novel Acid Promoted Side-Chain Deacylation of Pseudomycin A (Ia)." ChemInform 32, no. 17 (April 24, 2001): no. http://dx.doi.org/10.1002/chin.200117201.

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4

Ballio, A., F. Bossa, D. Di Giorgio, P. Ferranti, M. Paci, P. Pucci, A. Scaloni, A. Segre, and G. A. Strobel. "Novel bioactive lipodepsipeptides from Pseudomonas syringae : The pseudomycins." FEBS Letters 355, no. 1 (November 21, 1994): 96–100. http://dx.doi.org/10.1016/0014-5793(94)01179-6.

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5

Sun, Xicheng, Michael Rodriguez, Doug Zeckner, Bobbie Sachs, William Current, Robert Boyer, Jonathan Paschal, Carl McMillian, and Shu-Hui Chen. "Synthesis and Evaluation of Oxodioxolenylmethyl Carbamate Prodrugs of Pseudomycins." Journal of Medicinal Chemistry 44, no. 16 (August 2001): 2671–74. http://dx.doi.org/10.1021/jm000425w.

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6

Chen, S. H., and M. Rodriguez. "Antifungal lipopeptides: A tale of pseudomycin prodrugs and analogues." Drugs of the Future 28, no. 5 (2003): 441. http://dx.doi.org/10.1358/dof.2003.028.05.737309.

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7

Zhang, Yan-Zhi, Xicheng Sun, Douglas J. Zeckner, Roberta K. Sachs, William L. Current, and Shu-Hui Chen. "8-amido-bearing pseudomycin B (PSB) analogue: novel antifungal agents." Bioorganic & Medicinal Chemistry Letters 11, no. 2 (January 2001): 123–26. http://dx.doi.org/10.1016/s0960-894x(00)00606-5.

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8

Sun, Xicheng, Douglas J. Zeckner, Yan-zhi Zhang, Roberta K. Sachs, William L. Current, Michael Rodriguez, and Shu-Hui Chen. "Prodrugs of 3-amido bearing pseudomycin analogues: novel antifungal agents." Bioorganic & Medicinal Chemistry Letters 11, no. 14 (July 2001): 1881–84. http://dx.doi.org/10.1016/s0960-894x(01)00335-3.

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9

Sun, Xicheng, Douglas J. Zeckner, William L. Current, Robert Boyer, Carl McMillian, Nathan Yumibe, and Shu-Hui Chen. "N -Acyloxymethyl carbamate linked prodrugs of pseudomycins are novel antifungal agents." Bioorganic & Medicinal Chemistry Letters 11, no. 14 (July 2001): 1875–79. http://dx.doi.org/10.1016/s0960-894x(01)00333-x.

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10

Bhushan, B., and G. S. Hoondal. "Relationship between lipase production and pseudomycelia formation in a dimorphicCandida sp." World Journal of Microbiology & Biotechnology 13, no. 1 (January 1997): 129–30. http://dx.doi.org/10.1007/bf02770819.

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11

Zhang, Yanzhi, Robert Boyer, Xicheng Sun, Jonathan Paschal, and Shu-Hui Chen. "Serendipitous synthesis of novel dehydro- and dechloro-pseudomycin B (PSB) derivatives." Bioorganic & Medicinal Chemistry Letters 10, no. 8 (April 2000): 775–78. http://dx.doi.org/10.1016/s0960-894x(00)00096-2.

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12

Jamison, James, Stuart Levy, Xicheng Sun, Doug Zeckner, William Current, Mark Zweifel, Michael Rodriguez, William Turner, and Shu-Hui Chen. "Syntheses and antifungal activity of pseudomycin side-chain analogues. Part 1." Bioorganic & Medicinal Chemistry Letters 10, no. 18 (September 2000): 2101–5. http://dx.doi.org/10.1016/s0960-894x(00)00423-6.

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13

Zhang, Yan-Zhi, Xicheng Sun, Douglas J. Zeckner, Roberta K. Sachs, William L. Current, Jaswant Gidda, Michael Rodriguez, and Shu-Hui Chen. "Syntheses and antifungal activities of novel 3-amido bearing pseudomycin analogues." Bioorganic & Medicinal Chemistry Letters 11, no. 7 (April 2001): 903–7. http://dx.doi.org/10.1016/s0960-894x(01)00101-9.

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14

Sun, Xicheng, Yan-Zhi Zhang, Doug Zeckner, William Current, and Shu-Hui Chen. "Synthesis and evaluation of novel pseudomycin side-chain analogues. Part 3." Bioorganic & Medicinal Chemistry Letters 11, no. 23 (December 2001): 3055–59. http://dx.doi.org/10.1016/s0960-894x(01)00627-8.

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15

Di Giorgio, Domenico, Lorenzo Camoni, Camilla Marchiafava, and Alessandro Ballio. "Biological activities of pseudomycin a, a lipodepsinonapeptide from Pseudomonas syringae msu 16h." Phytochemistry 45, no. 7 (August 1997): 1385–91. http://dx.doi.org/10.1016/s0031-9422(97)00173-8.

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16

Chen, Shu-Hui, Xicheng Sun, Robert Boyer, Jonathan Paschal, Doug Zeckner, William Current, Mark Zweifel, and Michael Rodriguez. "Syntheses and biological evaluation of novel pseudomycin side-chain analogues. Part 2." Bioorganic & Medicinal Chemistry Letters 10, no. 18 (September 2000): 2107–10. http://dx.doi.org/10.1016/s0960-894x(00)00424-8.

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17

Zhang, Yan-Zhi, Xicheng Sun, Douglas J. Zeckner, Roberta K. Sachs, William L. Current, Jaswant Gidda, Michael Rodriguez, and Shu-Hui Chen. "ChemInform Abstract: Syntheses and Antifungal Activities of Novel 3-Amido Bearing Pseudomycin Analogues." ChemInform 32, no. 49 (May 23, 2010): no. http://dx.doi.org/10.1002/chin.200149251.

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18

Harrison, L., D. B. Teplow, M. Rinaldi, and G. Strobel. "Pseudomycins, a family of novel peptides from Pseudomonas syringae possessing broad-spectrum antifungal activity." Journal of General Microbiology 137, no. 12 (December 1, 1991): 2857–65. http://dx.doi.org/10.1099/00221287-137-12-2857.

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19

Sorensen, Kevin N., Kwang-Hee Kim, and Jon Y. Takemoto. "PCR Detection of Cyclic Lipodepsinonapeptide-Producing Pseudomonas syringae pv. syringae and Similarity of Strains." Applied and Environmental Microbiology 64, no. 1 (January 1, 1998): 226–30. http://dx.doi.org/10.1128/aem.64.1.226-230.1998.

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ABSTRACT Many strains of Pseudomonas syringae pv. syringae produce one of four classes of small cyclic lipodepsinonapeptides: syringomycins, syringostatins, syringotoxins, or pseudomycins. These metabolites are phytotoxic and growth inhibitory against a broad spectrum of fungi. Their production is dependent upon the expression of conserved biosynthesis and export genes syrB andsyrD, respectively. PCR and oligonucleotide primers specific for a 752-bp fragment of syrB were used to identify cyclic lipodepsinonapeptide-producing strains of P. syringae pv. syringae. In contrast, PCR amplification with primers based on syrD did not always correlate with possession of the syrD gene, as indicated by Southern blot analysis, or with cyclic lipodepsinonapeptide production. Sequence comparisons of 400 nucleotides from the syrB PCR-amplified fragments showed 94% plot similarity among 27 strains. In a sequence phenogram, syringostatin and syringotoxin producers were grouped apart from syringomycin-producing strain B301D, with sequences that differed by eight and nine conserved base substitutions, respectively. PCR amplification of the 752-bp syrB fragment offers rapid and accurate detection of cyclic lipodepsinonapeptide-producing strains, and its sequence provides some predictive capabilities for identifying syringotoxin and syringostatin producers.
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20

Bezuglova, O. S., V. E. Boldyreva, S. N. Gorbov, and Yu A. Litvinov. "Genetic Features of Soils on Dense Parent Rocks of the Donetsk Ridge." Почвоведение, no. 10 (October 1, 2023): 1205–15. http://dx.doi.org/10.31857/s0032180x23600075.

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The present study investigates morphological, physical and chemical properties of Chernozems at dense parent rocks. The research was carried out on the protected areas native soils of the north-west of the Rostov region. This territory is representing eastern slopes of the Donetsk Ridge, which predetermines the dense rocks release to the surface. It has been found that morphological, physical and chemical properties of Chernozems on dense rocks have emphasized their originality and uniqueness, and at the same time clearly have indicate their classification as Chernozem order. In comparison with the zonal soil – Calcic Chernozem – Chernozems on dense rocks are characterized by a reduced thickness of humus-accumulative layers, an increased of humus content, the presence of gravel in profile bottom half, a weak expression of calcareous accumulations, features of the particle-size distribution of soil components, even if it belongs to the same soil texture class. Chernozems on dense carbonate rocks either do not have accumulation or are characterized by a weak manifestation of secondary carbonates (pseudomycelia and nodules). This fact has differed such soil from the same order Chrernozems on fine-grained rocks (Calcic Chernozems) for which it is diagnostic criteria. Therefore, the mention of the suborder of these soils is incorrect in the designation. In the soil covering of the spurs of the Donetsk Ridge, dark humus soils are also occure, previously classified as incomplete developed chernozems, differing from chernozems by the absence of medium part of soil profiles.
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21

Elsayed, Mostafa Abdulla. "Oral itraconazole combined with local isoconazole in the treatment chronic candida vulvovaginitis." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 11, no. 8 (July 27, 2022): 2071. http://dx.doi.org/10.18203/2320-1770.ijrcog20221915.

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Background: Chronic vulvovaginal candidiasis is a major problem and common with poor quality of life from itching and discharge and it is difficult to treat because fungi are slow growers.Methods: Two hundred cases recruited from JAM clinic in Benha city, Egypt divided into two groups to study combination of oral itraconazole and local isoconazole in comparison with the use of local isoconazole only in chronic monilial vulvovaginitis and main outcome was relief of symptoms and signs with absent laboratory evidence of monilial infection by culture. Group one included 100 cases treated with combined oral itraconazole with three alternate days dose of local isoconazole (gynotrazonagen) and group two (local isoconazole only) included 100 cases treated with local isoconazole ovules on alternate days for 3 doses and week period.Results: Regarding the cure rate there were 90 clinically cured rate in the combined group compared to 70 in the local treatment group with p value of 0.0004 which was a very high statistically significant difference. Clinical cure included alleviation of the symptoms of discharge dysuria dyspareunia burning itching with also by clinical examination cure and disappearance of redness erythema edema fissures with absent pseudomycelia by microscopic examination. Usually, a symptom score of less than 2 is a positive one. Regarding the laboratory cure which means absent or negative candida culture on Sabaraud agar medium there were a laboratory cure rate of 84 out of 100 in the combined treatment group compared to 65 out of 100 in the local treatment group with p value of 0.002 and a high statistically significant difference.Conclusions: Oral itraconazole combined with local isoconazole is highly effective in treating chronic monilial vulvovaginitis.
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22

Coiro, Vincenza Maria, Anna Laura Segre, Alfredo Di Nola, Maurizio Paci, Alessandro Grottesi, Gianluigi Veglia, and Alessandro Ballio. "Solution conformation of the Pseudomonas syringae MSU 16H phytotoxic lipodepsipeptide Pseudomycin A determined by computer simulations using distance geometry and molecular dynamics from NMR data." European Journal of Biochemistry 257, no. 2 (October 15, 1998): 449–56. http://dx.doi.org/10.1046/j.1432-1327.1998.2570449.x.

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