Curvularin-Type Metabolites from the Fungus Curvularia sp Isolated from a Marine Alga

被引:49
作者
Dai, Jingqiu [1 ]
Krohn, Karsten [1 ]
Floerke, Ulrich [1 ]
Pescitelli, Gennaro [2 ]
Kerti, Gabor [3 ]
Papp, Tamas [3 ]
Koever, Katalin E. [4 ]
Benyei, Attila Csaba [5 ]
Draeger, Sigfried [6 ]
Schulz, Barabara [6 ]
Kurtan, Tibor [3 ]
机构
[1] Univ Gesamthsch Paderborn, Dept Chem, D-33098 Paderborn, Germany
[2] Univ Pisa, Dipartimento Chim & Chim Ind, I-56126 Pisa, Italy
[3] Univ Debrecen, Dept Organ Chem, H-4010 Debrecen, Hungary
[4] Univ Debrecen, Dept Inorgan & Analyt Chem, H-4010 Debrecen, Hungary
[5] Univ Debrecen, Lab Xray Diffract, H-4010 Debrecen, Hungary
[6] Tech Univ Carolo Wilhelmina Braunschweig, Inst Microbiol, D-31806 Braunschweig, Germany
基金
匈牙利科学研究基金会;
关键词
Natural products; Configuration determination; Fungal metabolites; Density functional calculations; Electronic circular dichroism; CITREO-VIRIDE-B; ABSOLUTE-CONFIGURATION; SECONDARY METABOLITES; CRYSTAL-STRUCTURES; IFO; 6200; PHOMA SP; DEHYDROCURVULARIN; 11-ALPHA-METHOXYCURVULARIN; STEREOCHEMISTRY; RHIZOSPHERE;
D O I
10.1002/ejoc.201001237
中图分类号
O62 [有机化学];
学科分类号
070303 [有机化学];
摘要
Two new curvularin-type macrolides, curvulone A (1) and B (2), and two known ones (3a, 4) of the rare 15R series have been isolated from the fungus Curvularia sp., which has been isolated from the marine alga Gracilaria folifera. Their structures were determined by extensive 2D NMR experiments and supported by the single-crystal X-ray analysis of 1. The structural elucidation of 1, which has a benzo[b]furanone moiety as part of a 12-membered macrolactone, has led to a revision of the structure of the previously reported (11S,15S)-11 beta-hydroxy-12-oxocurvularin. The absolute configuration of curvulone A was established independently by the solidstate TD-DFT ECD method and by measuring the anomalous dispersion effect. The absolute configuration of curvulone B was determined by TD-DFT ECD calculations on the computed solution conformers. Two different solid-state conformers of 4 were identified by X-ray analysis of the single crystals obtained from different solvents; TD-DFT ECD calculations were performed to reproduce the experimental ECD spectra. All four metabolites were biologically active against fungal, bacterial and algal test organisms.
引用
收藏
页码:6928 / 6937
页数:10
相关论文
共 48 条
[1]
The Cambridge Structural Database: a quarter of a million crystal structures and rising [J].
Allen, FH .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 2002, 58 (3 PART 1) :380-388
[2]
STRUCTURAL STUDY OF DEHYDROCURVULARIN, AN INHIBITOR OF MICROTUBULE ASSEMBLY [J].
ALMASSI, F ;
GHISALBERTI, EL ;
SKELTON, BW ;
WHITE, AH .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1994, 47 (06) :1193-1197
[3]
COMPLETION AND REFINEMENT OF CRYSTAL-STRUCTURES WITH SIR92 [J].
ALTOMARE, A ;
CASCARANO, G ;
GIACOVAZZO, C ;
GUAGLIARDI, A .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1993, 26 (pt 3) :343-350
[4]
[Anonymous], 2002, SMART VERS 5 62 SAIN
[5]
[Anonymous], SPART 08
[6]
BIOSYNTHESES OF ANTIBIOTIC A26771B BY PENICILLIUM-TURBATUM AND DEHYDROCURVULARIN BY ALTERNARIA-CINERARIAE - COMPARISON OF STEREOCHEMISTRY OF POLYKETIDE AND FATTY-ACID ENOYL THIOL ESTER REDUCTASES [J].
ARAI, K ;
RAWLINGS, BJ ;
YOSHIZAWA, Y ;
VEDERAS, JC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (09) :3391-3399
[7]
Computing Chiroptical Properties with First-Principles Theoretical Methods: Background and Illustrative Examples [J].
Autschbach, Jochen .
CHIRALITY, 2009, 21 (1E) :E116-E152
[8]
Bicalho B, 2003, Z NATURFORSCH C, V58, P746
[9]
Ebel R, 2010, COMPREHENSIVE NATURAL PRODUCTS II: CHEMISTRY AND BIOLOGY, VOL 2: NATURAL PRODUCTS STRUCTURAL DIVERSITY-II: SECONDARY METABOLITES: SOURCES, STRUCTURES AND CHEMICAL BIOLOGY, P223
[10]
Ernst RR., 1987, Two-Dimensional NMR Spectroscopy, P1