School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, New South Wales, Australia.
ISME J. 2012 Oct;6(10):1834-47. doi: 10.1038/ismej.2012.25. Epub 2012 Mar 29.
The nitrogen-fixing bacterium, Nostoc, is a commonly occurring cyanobacterium often found in symbiotic associations. We investigated the potential of cycad cyanobacterial endosymbionts to synthesize microcystin/nodularin. Endosymbiont DNA was screened for the aminotransferase domain of the toxin biosynthesis gene clusters. Five endosymbionts carrying the gene were screened for bioactivity. Extracts of two isolates inhibited protein phosphatase 2A and were further analyzed using electrospray ionization mass spectrometry (ESI-MS)/MS. Nostoc sp. 'Macrozamia riedlei 65.1' and Nostoc sp. 'Macrozamia serpentina 73.1' both contained nodularin. High performance liquid chromatography (HPLC) HESI-MS/MS analysis confirmed the presence of nodularin at 9.55±2.4 ng μg-1 chlorophyll a in Nostoc sp. 'Macrozamia riedlei 65.1' and 12.5±8.4 ng μg-1 Chl a in Nostoc sp. 'Macrozamia serpentina 73.1' extracts. Further scans indicated the presence of the rare isoform [L-Har(2)] nodularin, which contains L-homoarginine instead of L-arginine. Nodularin was also present at 1.34±0.74 ng ml(-1) (approximately 3 pmol per g plant ww) in the methanol root extracts of M. riedlei MZ65, while the presence of [L-Har(2)] nodularin in the roots of M. serpentina MZ73 was suggested by HPLC HESI-MS/MS analysis. The ndaA-B and ndaF genomic regions were sequenced to confirm the presence of the hybrid polyketide/non-ribosomal gene cluster. A seven amino-acid insertion into the NdaA-C1 domain of N. spumigena NSOR10 protein was observed in all endosymbiont-derived sequences, suggesting the transfer of the nda cluster from N. spumigena to terrestrial Nostoc species. This study demonstrates the synthesis of nodularin and [L-Har(2)] nodularin in a non-Nodularia species and the production of cyanobacterial hepatotoxin by a symbiont in planta.
固氮细菌念珠藻是一种常见的共生蓝藻。我们研究了苏铁蓝藻内共生体合成微囊藻毒素/节球藻毒素的潜力。对共生体 DNA 进行了毒素生物合成基因簇的氨基转移酶结构域筛选。从携带该基因的 5 个内共生体中筛选出生物活性。两种分离物的提取物抑制蛋白磷酸酶 2A,并进一步使用电喷雾电离质谱(ESI-MS)/MS 进行分析。 Nostoc sp。'Macrozamia riedlei 65.1'和 Nostoc sp。'Macrozamia serpentina 73.1'都含有节球藻毒素。高效液相色谱(HPLC)HESI-MS/MS 分析证实 Nostoc sp。'Macrozamia riedlei 65.1'中节球藻毒素的存在量为 9.55±2.4ngμg-1叶绿素 a,Nostoc sp。'Macrozamia serpentina 73.1'提取物中节球藻毒素的存在量为 12.5±8.4ngμg-1 Chl a。进一步扫描表明存在罕见的同型物[L-Har(2)]节球藻毒素,其中含有 L-高精氨酸而不是 L-精氨酸。在 M. riedlei MZ65 的甲醇根提取物中也存在节球藻毒素,含量为 1.34±0.74ngml(-1)(约 3pmol per g 植物 ww),而通过 HPLC HESI-MS/MS 分析表明 M. serpentina MZ73 根中存在[L-Har(2)]节球藻毒素。对 ndaA-B 和 ndaF 基因组区域进行了测序,以确认杂种聚酮/非核糖体基因簇的存在。在所有内共生体衍生序列中,都观察到 N. spumigena NSOR10 蛋白的 NdaA-C1 结构域中有七个氨基酸插入,这表明 nda 簇从 N. spumigena 转移到陆地念珠藻物种。本研究证明了非节球藻物种中节球藻毒素和[L-Har(2)]节球藻毒素的合成以及植物内共生体产生的蓝藻肝毒素。