Trans-4-aminoproline, a phytotoxic metabolite with herbicidal activity produced by Ascochyta caulina

被引:36
作者
Evidente, A
Andolfi, A
Vurro, M
Zonno, MC
Motta, A
机构
[1] Univ Naples Federico II, Dipartimento Sci Chimagr, I-80055 Portici, Italy
[2] CNR, Ist Tossine & Micotossine Parassiti Vegetali, I-70125 Bari, Italy
[3] CNR, Ist Chim Mol Interesse Biol, I-80072 Arco, Italy
关键词
Chenopodium album; Ascochyta caulina; phytotoxins; nonproteigenic amino acids; trans-4-aminoproline; weed biocontrol;
D O I
10.1016/S0031-9422(99)00507-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A phytotoxic metabolite, characterized through NMR techniques and synthetic methods as trans-4-aminoproline, was isolated from the culture filtrates of Ascochyta caulina, a promising mycoherbicide for biological control of Chenopodium album. The metabolite, which shows interesting phytotoxic properties, together with ascaulitoxin (recently characterized as N-2-beta-D-glucoside of the unusual bis-amino acid 2,4,7-triamino-5-hydroxyoctandioc acid) and another unidentified compound, compose an active fraction of A. caulina culture filtrates with promising herbicidal properties. When assayed on leaves of host and non host dicots, including wild and cultivated plants, the trans-4-aminoproline showed a wide range of toxicity, with leaves of C. album being the most sensitive. Other interesting aspects were its inefficacy on several monocots, both cultivated and wild and its lack of antifungal, antibiotic and zootoxic activities. This is the first report on trans-4-aminoproline as naturally occurring compound and phytotoxic metabolite produced by A. caulina. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:231 / 237
页数:7
相关论文
共 22 条
[1]   SYNTHESIS OF CIS AND TRANS ISOMERS OF 4-CHLORO-L-PROLINE 4-BROMO-L-PROLINE AND 4-AMINO-L-PROLINE [J].
ANDREATTA, RH ;
NAIR, V ;
ROBERTSON, AV ;
SIMPSON, WRJ .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1967, 20 (07) :1493-+
[2]  
[Anonymous], 1977, WORLDS WORST WEEDS
[3]   H-1 AND C-13 ASSIGNMENTS FROM SENSITIVITY-ENHANCED DETECTION OF HETERONUCLEAR MULTIPLE-BOND CONNECTIVITY BY 2D MULTIPLE QUANTUM NMR [J].
BAX, A ;
SUMMERS, MF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (08) :2093-2094
[4]   COMPARISON OF DIFFERENT MODES OF 2-DIMENSIONAL REVERSE-CORRELATION NMR FOR THE STUDY OF PROTEINS [J].
BAX, A ;
IKURA, M ;
KAY, LE ;
TORCHIA, DA ;
TSCHUDIN, R .
JOURNAL OF MAGNETIC RESONANCE, 1990, 86 (02) :304-318
[5]   INVESTIGATION OF COMPLEX NETWORKS OF SPIN-SPIN COUPLING BY TWO-DIMENSIONAL NMR [J].
BAX, A ;
FREEMAN, R .
JOURNAL OF MAGNETIC RESONANCE, 1981, 44 (03) :542-561
[6]  
Bottalico A., 1989, Fusarium: mycotoxins, taxonomy and pathogenicity., P85
[7]  
BREITMAIER E, 1987, CARBON 13 NMR SPECTR, P80
[8]   Ascaulitoxin, a phytotoxic bis-amino acid N-glucoside from Ascochyta caulina [J].
Evidente, A ;
Capasso, R ;
Cutignano, A ;
Taglialatela-Scafati, O ;
Vurro, M ;
Zonno, MC ;
Motta, A .
PHYTOCHEMISTRY, 1998, 48 (07) :1131-1137
[9]  
FANG SD, 1961, SCI SINICA, V10, P845
[10]   A NEW AMINO ACID ISOLATED FROM MORCHELLA ESCULENTA AND RELATED SPECIES [J].
HATANAKA, SI .
PHYTOCHEMISTRY, 1969, 8 (07) :1305-&