Triterpene saponin hemi-biosynthesis of a leaf beetle’s (<Emphasis Type="Italic">Platyphora kollari</Emphasis>) defensive secretion

The adults of the leaf beetle Platyphora kollari (Chrysomelidae) are able to metabolise the oleanane triterpene β-amyrin (1) into the glycoside 3-O-β-d-glucopyranosyl-(1→4)-β-d-glucuronopyranosyl-hederagenin (2) that is stored in their defensive glands. The aim of this study was to test the hypothesis that oleanolic acid (3) is an intermediate in the conversion of 1 into 2 and to check whether the sequestration of pentacyclic triterpenes is selective in favour of β-amyrin (1). To this end, adults of P. kollari were fed with Ipomoea batatas leaf disks painted with a solution of [2,2,3-²H₃]oleanolic acid or [2,2,3-²H₃]α-amyrin and the secretion of their defensive glands analysed by HPLC–ESIMS. The data presented in this work indicated that the first step of the transformation of β-amyrin (1) into the sequestered glycoside 2 is its oxidation into oleanolic acid (3) and that this conversion is selective but not specific in favour of β-amyrin (1).     

刺茶美登木的化学成分研究

从刺茶美登木地上部分的95%乙醇提取物中分离并鉴定了27个化合物:prinsepiol(1),( )-松脂醇(2),(-)-松脂醇(3),(-)-丁香树脂醇(4),( )-cycloolivil(5),(-)-橄榄树脂素(6),1-羟基-松脂醇(7),ilelatifolD(8),东莨菪素(9),β-香树素乙酸酯(10),α-香树素乙酸酯(11),fupenzicacid(12),( )-儿茶素(13),secoisolariciresinol(14),软脂酸-1-甘油单酯(15),植物醇(16),咖啡酸(17),3,4-二甲氧基肉桂酸(18),(-)-massoniresinol(19),tanegool(20),β-谷甾醇(21),羽扇豆醇(22),白桦酯醇(23),β-胡萝卜甙(24),齐墩果酸(25),熊果酸(26)和(-)-橄榄树脂素乙酸酯(27).图1表1参34     

爵床的化学成分研究

为了研究爵床全草中具有血管紧张素转化酶抑制活性的化学成分,从爵床全草95%乙醇提取物中分离并鉴定了13个化合物:芹菜素(1)、槲皮素7-O-α-L-吡喃鼠李糖甙(2)、木犀草素7-O-β-D-吡喃葡萄糖甙(3)、洋芹素7-O-β-D-吡喃葡萄糖甙(4)、洋芹素7-O-新橙皮甙(5)、β-谷甾醇(6)、β-胡萝卜甙(7)、东莨菪素(8)、羽扇豆醇乙酸酯(9)、环桉烯醇(10)、木栓酮(11)、木栓醇(12)、积雪草酸(13).HPLC检测结果证明,该植物中还存在木犀草素(14)和槲皮素(15).其中化合物1、14和15为爵床中具有血管紧张素转化酶抑制活性的成分.图1表2参28     

Pyrrolizidine alkaloids and pentacyclic triterpene saponins in the defensive secretions of Platyphora leaf beetles

Summary. Field collected exocrine defensive secretions of nine neotropical Platyphora species were analyzed for the presence of plant acquired pyrrolizidine alkaloids (PAs) and pentacyclic triterpene saponins. All species secrete saponins. In addition, five species feeding on Tournefortia (Boraginaceae), Koanophyllon (Asteraceae, tribe Eupatorieae) and Prestonia (Apocynaceae) were shown to sequester PAs of the lycopsamine type, which are characteristic for species of the three plant families. The PA sequestering species commonly store intermedine, lycopsamine and their O^3′-acetyl or propionyl esters as well as O⁷- and O⁹-hydroxyisovaleryl esters of retronecine. The latter as well as the O^3′-acyl esters were not found in the beetles’ host plants, suggesting the ability of the beetles to esterify plant derived retronecine and intermedine or its stereoisomers. Despite the conformity of the beetles’ PA patterns, considerable inconsistencies exist regarding the PA patterns of the respective host plants. One host plant was devoid of PAs, while another contained only simple necines. Since the previous history of the field collected beetles was unknown this discrepancy remains obscure. In contrast to the Palearctic chrysomeline leaf beetles, e.g. some Oreina species which ingest and store PAs as their non-toxic N-oxides, Platyphora leaf beetles absorb and store PAs as the toxic free base (tertiary PA), but apparently avoid to accumulate PAs in the haemolymph. This suggests that Chrysolina and Platyphora leaf beetles developed different lines of adaptations in their parallel evolution of PA mediated chemical defense. Received 30 November 2000; accepted 5 February 2001     

Larvicidal potential of different solvent extracts and oleanolic acid derivative from Coccinia indica against vector mosquitoes

The mosquito larvicidal activities of different solvent extracts (chloroform, ethyl acetate, and methanol) from the leaves of Coccinia indica were studied. Among the extracts tested, the methanol extract showed the highest larvicidal activity against early fourth instar larvae of Culex quinquefasciatus (LC₅₀?=?142?mg?L^?1), Aedes aegypti (LC₅₀?=?158?mg?L^?1) and Anopheles stephensi (LC₅₀?=?161?mg?L^?1) after 24?h of exposure period. The lowest larval mortality was observed with the ethyl acetate extract with the LC₅₀ values of 927, 872, and 730?mg?L^?1 against Cx. quinquefasciatus, Ae. aegypti, and An. stephensi, respectively. The chloroform extract showed the moderate larvicidal activity against the mosquito species tested with the LC₅₀ values from 446 to 546?mg?L^?1. A new triterpene was isolated from the methanol extract using bio-assay guided separation and identified as an oleanolic acid derivative by NMR, IR and mass spectral studies. The compound showed prominent larvicidal activity against Cx. quinquefasciatus, Ae. aegypti and An. stephensi with the LC₅₀ values of 5.6, 5.0, and 4.8?mg?L^?1, respectively. The results of the present investigation offer an opportunity for developing alternatives to rather expensive and environmentally hazardous organic insecticides.     

弯茎还阳参的化学成分

从弯茎还阳参全草中首次分离得到12个化合物,通过理化性质和波谱数据,分别鉴定为对羟基苯甲酸(1)、对羟基苯甲酸乙酯(2)、20(30)-烯-3β,21α-双羟基蒲公英烷(3)、秦皮乙素(4)、乌素酸(5)、齐墩果酸(6)、芹菜素(7)、木犀草素(8)、二十八烷酸(9)、二十五烷酸α单甘油酯(10)、胡萝卜苷(11)和木犀草素-7-葡萄糖苷(12).其中,化合物3、4、5、8在体外对小鼠黑色素瘤B16具有抑制作用.参17