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Biosynthetic Studies of Phomopsins Unveil Posttranslational Installation of Dehydroamino Acids by UstYa Family Proteins.

Angewandte Chemie (International ed. in English)

Sogahata K, Ozaki T, Igarashi Y, Naganuma Y, Liu C, Minami A, Oikawa H.
PMID: 34608734
Angew Chem Int Ed Engl. 2021 Dec 01;60(49):25729-25734. doi: 10.1002/anie.202111076. Epub 2021 Nov 03.

UstYa family proteins (DUF3328) are widely and specifically distributed in fungi. They are known to be involved in the biosynthesis of ribosomally synthesized and posttranslationally modified peptides (RiPPs) and nonribosomal peptides, and possibly catalyze various reactions, including oxidative cyclization...

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Sogahata K, Ozaki T, Igarashi Y, et al. Biosynthetic Studies of Phomopsins Unveil Posttranslational Installation of Dehydroamino Acids by UstYa Family Proteins. Angew Chem Int Ed Engl. 2021;60(49):25729-25734doi: 10.1002/anie.202111076.
Sogahata, K., Ozaki, T., Igarashi, Y., Naganuma, Y., Liu, C., Minami, A., & Oikawa, H. (2021). Biosynthetic Studies of Phomopsins Unveil Posttranslational Installation of Dehydroamino Acids by UstYa Family Proteins. Angewandte Chemie (International ed. in English), 60(49), 25729-25734. https://doi.org/10.1002/anie.202111076
Sogahata, Kaho, et al. "Biosynthetic Studies of Phomopsins Unveil Posttranslational Installation of Dehydroamino Acids by UstYa Family Proteins." Angewandte Chemie (International ed. in English) vol. 60,49 (2021): 25729-25734. doi: https://doi.org/10.1002/anie.202111076
Sogahata K, Ozaki T, Igarashi Y, Naganuma Y, Liu C, Minami A, Oikawa H. Biosynthetic Studies of Phomopsins Unveil Posttranslational Installation of Dehydroamino Acids by UstYa Family Proteins. Angew Chem Int Ed Engl. 2021 Dec 01;60(49):25729-25734. doi: 10.1002/anie.202111076. Epub 2021 Nov 03. PMID: 34608734.
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A Copper-Carbodiimide Approach to the Phomopsin Tripeptide Side Chain.

Tetrahedron letters

Shangguan N, Joullié M.
PMID: 20802791
Tetrahedron Lett. 2009 Dec 09;50(49):6748-6750. doi: 10.1016/j.tetlet.2009.09.072.

No abstract available.

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Shangguan N, Joullié M. A Copper-Carbodiimide Approach to the Phomopsin Tripeptide Side Chain. Tetrahedron Lett. 2009;50(49):6748-6750doi: 10.1016/j.tetlet.2009.09.072.
Shangguan, N., & Joullié, M. (2009). A Copper-Carbodiimide Approach to the Phomopsin Tripeptide Side Chain. Tetrahedron letters, 50(49), 6748-6750. https://doi.org/10.1016/j.tetlet.2009.09.072
Shangguan, Ning, and Joullié, Madeleine. "A Copper-Carbodiimide Approach to the Phomopsin Tripeptide Side Chain." Tetrahedron letters vol. 50,49 (2009): 6748-6750. doi: https://doi.org/10.1016/j.tetlet.2009.09.072
Shangguan N, Joullié M. A Copper-Carbodiimide Approach to the Phomopsin Tripeptide Side Chain. Tetrahedron Lett. 2009 Dec 09;50(49):6748-6750. doi: 10.1016/j.tetlet.2009.09.072. PMID: 20802791; PMCID: PMC2926967.
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Synthesis of TMPA Derivatives through Sequential Ir(III)-Catalyzed C-H Alkylation and Their Antidiabetic Evaluation.

ACS omega

Lee SH, Kundu A, Han SH, Mishra NK, Kim KS, Choi MH, Pandey AK, Park JS, Kim HS, Kim IS.
PMID: 30023845
ACS Omega. 2018 Mar 31;3(3):2661-2672. doi: 10.1021/acsomega.8b00179. Epub 2018 Mar 06.

The synthesis and antidiabetic evaluation of ethyl 2-[2,3,4-trimethoxy-6-(1-octanoyl)phenyl]acetate (TMPA) and its structural analogs are described. The construction of TMPA derivatives has been successfully achieved in only two steps, which involve the iridium(III)-catalyzed α-alkylation of acetophenones with alcohols and the...

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Lee SH, Kundu A, Han SH, et al. Synthesis of TMPA Derivatives through Sequential Ir(III)-Catalyzed C-H Alkylation and Their Antidiabetic Evaluation. ACS Omega. 2018;3(3):2661-2672doi: 10.1021/acsomega.8b00179.
Lee, S. H., Kundu, A., Han, S. H., Mishra, N. K., Kim, K. S., Choi, M. H., Pandey, A. K., Park, J. S., Kim, H. S., & Kim, I. S. (2018). Synthesis of TMPA Derivatives through Sequential Ir(III)-Catalyzed C-H Alkylation and Their Antidiabetic Evaluation. ACS omega, 3(3), 2661-2672. https://doi.org/10.1021/acsomega.8b00179
Lee, Suk Hun, et al. "Synthesis of TMPA Derivatives through Sequential Ir(III)-Catalyzed C-H Alkylation and Their Antidiabetic Evaluation." ACS omega vol. 3,3 (2018): 2661-2672. doi: https://doi.org/10.1021/acsomega.8b00179
Lee SH, Kundu A, Han SH, Mishra NK, Kim KS, Choi MH, Pandey AK, Park JS, Kim HS, Kim IS. Synthesis of TMPA Derivatives through Sequential Ir(III)-Catalyzed C-H Alkylation and Their Antidiabetic Evaluation. ACS Omega. 2018 Mar 31;3(3):2661-2672. doi: 10.1021/acsomega.8b00179. Epub 2018 Mar 06. PMID: 30023845; PMCID: PMC6045468.
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Growth and toxin production of phomopsin A and ochratoxin A forming fungi under different storage conditions in a pea (Pisum sativum) model system.

Mycotoxin research

Kunz BM, Pförtner L, Weigel S, Rohn S, Lehmacher A, Maul R.
PMID: 34921667
Mycotoxin Res. 2021 Dec 18; doi: 10.1007/s12550-021-00446-8. Epub 2021 Dec 18.

Phomopsins are mycotoxins mainly infesting lupines, with phomopsin A (PHOA) being the main mycotoxin. PHOA is produced by Diaporthe toxica, formerly assigned as toxigenic Phomopsis leptostromiformis, causing infections in lupine plants and harvested seeds. However, Diaporthe species may also...

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Kunz BM, Pförtner L, Weigel S, et al. Growth and toxin production of phomopsin A and ochratoxin A forming fungi under different storage conditions in a pea (Pisum sativum) model system. Mycotoxin Res. 2021;doi: 10.1007/s12550-021-00446-8.
Kunz, B. M., Pförtner, L., Weigel, S., Rohn, S., Lehmacher, A., & Maul, R. (2021). Growth and toxin production of phomopsin A and ochratoxin A forming fungi under different storage conditions in a pea (Pisum sativum) model system. Mycotoxin research, . https://doi.org/10.1007/s12550-021-00446-8
Kunz, Birgitta Maria, et al. "Growth and toxin production of phomopsin A and ochratoxin A forming fungi under different storage conditions in a pea (Pisum sativum) model system." Mycotoxin research vol. (2021). doi: https://doi.org/10.1007/s12550-021-00446-8
Kunz BM, Pförtner L, Weigel S, Rohn S, Lehmacher A, Maul R. Growth and toxin production of phomopsin A and ochratoxin A forming fungi under different storage conditions in a pea (Pisum sativum) model system. Mycotoxin Res. 2021 Dec 18; doi: 10.1007/s12550-021-00446-8. Epub 2021 Dec 18. PMID: 34921667.
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Showing 1 to 4 of 4 entries