4.6 Article

Novel toxins produced by the dinoflagellate Karenia brevisulcata

期刊

HARMFUL ALGAE
卷 13, 期 -, 页码 47-57

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.hal.2011.10.002

关键词

Brevetoxins; Brevisulcatic acids; BSX; Karenia brevisulcata; KBT; Toxic dinoflagellate

资金

  1. NZ Ministry for Science and Innovation [CAWX0703, CAWX0804]
  2. Japan Society for Promotion of Science [22404006]
  3. Grants-in-Aid for Scientific Research [22404006] Funding Source: KAKEN
  4. New Zealand Ministry of Business, Innovation & Employment (MBIE) [CAWX0804] Funding Source: New Zealand Ministry of Business, Innovation & Employment (MBIE)

向作者/读者索取更多资源

Karenia brevisulcata (Chang), a new toxic dinoflagellate of the genus Karenia was isolated from a harmful algal bloom that occurred in Wellington Harbour, New Zealand in 1998. The bloom severely affected most marine biota resulting in long-term ecological damage and causing respiratory distress in harbour bystanders. Cultures of K. brevisulcata produced a range of novel toxins including ten lipid-soluble K. brevisulcata toxins (KBTs) and six water-soluble brevisulcatic acids (BSXs). Brevetoxins were not detected. KBT-F, KBT-G, BSX-1 and BSX-2 were isolated from 1450 L of bulk cultures and purified in mg quantities. Preliminary chemical and toxicological investigations show that KBT-F (M 2054 C107H160O38) and KBT-G (M 2084 C108H162O39) are complex polycyclic ethers with UVmax at 227 nm. NMR data gave characteristics of ladder frame polyether structures and a 2-methylbut-2-enal side chain, similar to gymnocins. The mouse i.p. LD(50)s for KBT-F and -G were 0.032 and 0.040 mg kg(-1), respectively. These KBTs were also highly cytotoxic and haemolytic. BSX-1 (M 916 C49H72O16) and BSX-2 (M 872 C47H68O15) are polycyclic ether dicarboxylates with UVmax 196 nm. BSX-4 and BSX-5, the lactone ring-closed analogues and the presumed primary toxins in the algal cells, were isolated in smaller quantities. Preliminary structural information from NMR and MS showed a carboxylated side chain and some similarities to brevetoxin-A. However, the structures have not yet been fully elucidated due to conformers confounding the NMR. The mouse i.p. LD50 for BSX-1 was 3.9 mg kg(-1) while no deaths were seen in mice injected with BSX-2 at 6.6 mg kg(-1). The LD(50)s for the lactones BSX-4 and -5 were 1.4 and 1.6 mg kg(-1) respectively. BSX-4 and -5 were agonists of voltage-gated sodium channels but only weakly haemolytic. Activities in the Neuro-2a cytotoxicity assay were ca 10% of dihydrobrevetoxin-2 and were fully antagonised by saxitoxin. (C) 2011 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据