Your browser doesn't support javascript.
loading
Diverse polyketides from the marine endophytic Alternaria sp. LV52: Structure determination and cytotoxic activities.
Mahmoud, Manar M; Abdel-Razek, Ahmed S; Soliman, Hesham S M; Ponomareva, Larissa V; Thorson, Jon S; Shaaban, Khaled A; Shaaban, Mohamed.
Afiliação
  • Mahmoud MM; Pharmacognosy Department, Faculty of Pharmacy, Helwan University, Helwan City-Cairo 11884, Egypt.
  • Abdel-Razek AS; Organic and Bioorganic Chemistry, Faculty of Chemistry, Bielefeld University, d-33501 Bielefeld, Germany.
  • Soliman HSM; Organic and Bioorganic Chemistry, Faculty of Chemistry, Bielefeld University, d-33501 Bielefeld, Germany.
  • Ponomareva LV; Microbial Chemistry Department, Division of Genetic Engineering and Biotechnology Research, National Research Centre, El-Buhouth St. 33, Dokki-Cairo 12622, Egypt.
  • Thorson JS; Pharmacognosy Department, Faculty of Pharmacy, Helwan University, Helwan City-Cairo 11884, Egypt.
  • Shaaban KA; Pharm D program, Egypt-Japan University of Science and Technology (E-JUST), New Borg El-Arab City, 21934 Alexandria, Egypt.
  • Shaaban M; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States.
Biotechnol Rep (Amst) ; 33: e00628, 2022 Mar.
Article em En | MEDLINE | ID: mdl-35036335
ABSTRACT
We report the isolation and characterization of five polyketides [alternariol (1), alternariol-9-methyl ether (2), altertoxin I (3), altertoxin II (4) and tenuazonic acid (5)] from the marine endophytic Alternaria sp. LV52 derived from Cystoseira tamariscifolia, collected from the Red Sea at Nabq-Bay, Egypt. The chemical structures of compounds 1-5 were identified by extensive 1D, 2D NMR, and HR mass measurements. Isolation and phenotypic and genotypic characterization of the producing fungus is reported. The antimicrobial activity of the produced extract and derived compounds was examined against a panel of test organisms. In addition, an in vitro cytotoxic activity of 1-5 was performed against diverse cancer cell lines HEPG2, HELA, A549 and PC3, revealing that compounds 2 and 4 are potentially cytotoxic against A549 and PC3 with EC50 of 0.73 µg/ml (2.69 µM) and 0.17 µg/ml (0.64 µM) for 2, and 0.40 µg/ml (1.15 µM) and 0.12 µg/ml (0.33 µM) for 4, respectively.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biotechnol Rep (Amst) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biotechnol Rep (Amst) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito