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Journal articles on the topic 'Pseudomycena'

Author: Grafiati
Published: 29 July 2024
Last updated: 31 July 2025

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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 (1995): 1056–57. http://dx.doi.org/10.1080/11263509509440933.

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2

Rodriguez, Michael J., Matthew Belvo, Robert Morris, et al. "The synthesis of pseudomycin C′ via a novel acid promoted side-chain deacylation of pseudomycin A." Bioorganic & Medicinal Chemistry Letters 11, no. 2 (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, et al. "ChemInform Abstract: Synthesis of Pseudomycin C′ (Ib) via a Novel Acid Promoted Side-Chain Deacylation of Pseudomycin A (Ia)." ChemInform 32, no. 17 (2001): no. http://dx.doi.org/10.1002/chin.200117201.

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4

Ballio, A., F. Bossa, D. Di Giorgio, et al. "Novel bioactive lipodepsipeptides from Pseudomonas syringae : The pseudomycins." FEBS Letters 355, no. 1 (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, et al. "Synthesis and Evaluation of Oxodioxolenylmethyl Carbamate Prodrugs of Pseudomycins." Journal of Medicinal Chemistry 44, no. 16 (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 (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, et al. "Prodrugs of 3-amido bearing pseudomycin analogues: novel antifungal agents." Bioorganic & Medicinal Chemistry Letters 11, no. 14 (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, et al. "N -Acyloxymethyl carbamate linked prodrugs of pseudomycins are novel antifungal agents." Bioorganic & Medicinal Chemistry Letters 11, no. 14 (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 (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 (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, et al. "Syntheses and antifungal activity of pseudomycin side-chain analogues. Part 1." Bioorganic & Medicinal Chemistry Letters 10, no. 18 (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, et al. "Syntheses and antifungal activities of novel 3-amido bearing pseudomycin analogues." Bioorganic & Medicinal Chemistry Letters 11, no. 7 (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 (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 (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, et al. "Syntheses and biological evaluation of novel pseudomycin side-chain analogues. Part 2." Bioorganic & Medicinal Chemistry Letters 10, no. 18 (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, et al. "ChemInform Abstract: Syntheses and Antifungal Activities of Novel 3-Amido Bearing Pseudomycin Analogues." ChemInform 32, no. 49 (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 (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 (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 w
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20

Zambare, Rutuja, Vaidehi Bhagwat, Shivangni Singh, et al. "Microcycle Conidia Production in an Entomopathogenic Fungus Beauveria bassiana: The Role of Chitin Deacetylase in the Conidiation and the Contribution of Nanocoating in Conidial Stability." Microorganisms 13, no. 4 (2025): 900. https://doi.org/10.3390/microorganisms13040900.

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In the field, substantial quantities of insect pathogenic fungal conidia (5 × 1012/ha) are usually applied for the control of pests. In this regard, attempts are being made to obtain higher yields of conidia to make the process viable. One of the approaches is to induce microcycle conidia (MC) production. In a solid-state fermentation on rice, the SYB-grown inoculum with more pseudomycelia of B. bassiana enhanced MC production almost 5 times compared to the aerial conidia (AC) within 10 days. A chitosan (CNP) and alginate–chitosan (ACNP) nanocoating of MC increased the overall temperature and
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21

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 wit
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22

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 (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 comb
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23

Coiro, Vincenza Maria, Anna Laura Segre, Alfredo Di Nola, et al. "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 (1998): 449–56. http://dx.doi.org/10.1046/j.1432-1327.1998.2570449.x.

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