Harada Ken-ichi, Nakano Tomoyo, Fujii Kiyonaga, Shirai Makoto
Laboratory of Instrumental and Analytical Chemistry, Faculty of Pharmacy, Meijo University, Tempaku, Nagoya 468-8503, Japan.
J Chromatogr A. 2004 Apr 9;1033(1):107-13. doi: 10.1016/j.chroma.2004.01.006.
Microcystins are hepatotoxic heptapeptides and general tumor promoters produced by several species of the genera Microcystis, Anabaena, Oscillatoria and Nostoc. They are non-ribosomally synthesized via a mixed polyketide synthase/non-ribosomal peptide synthetase system called microcystin synthetase. We have carried out the detection, isolation and structural determination of non-toxic peptides produced together with microcystins by toxic cyanobacteria, which are classified into several groups on the basis of their structures and some of these non-toxic peptides are also non-ribosomally synthesized as well as microcystins. In the present study, we tried to correlate the secondary metabolic peptides produced by the hepatotoxic cyanobacteria with the corresponding peptide synthetase genes. An analytical method using LC-electroscopy ionization MS and photodiode array detection was developed for the exhaustive screening of cyanobacterial peptides in Japanese strains and it was successfully applied to the peptide fractions extracted from these strains. The established method was advantageous over conventional ones using the usual HPLC and matrix-assisted laser desorption ionization time-of-flight MS, because more structural information could be obtained and it is easier to distinguish microcystins from other peptides using this method. Small amounts of other peptides could also be detected by this method. The established method will contribute to the investigation of the relationship between genes encoding the peptide synthetase and secondary metabolic peptides.
微囊藻毒素是由微囊藻属、鱼腥藻属、颤藻属和念珠藻属的几种物种产生的具有肝毒性的七肽和一般肿瘤促进剂。它们通过一种称为微囊藻毒素合成酶的混合聚酮合酶/非核糖体肽合成酶系统进行非核糖体合成。我们已经对有毒蓝藻与微囊藻毒素一起产生的无毒肽进行了检测、分离和结构测定,这些无毒肽根据其结构分为几组,其中一些无毒肽也与微囊藻毒素一样通过非核糖体合成。在本研究中,我们试图将肝毒性蓝藻产生的次生代谢肽与相应的肽合成酶基因联系起来。开发了一种使用液相色谱-电喷雾电离质谱和光电二极管阵列检测的分析方法,用于对日本菌株中的蓝藻肽进行详尽筛选,并成功应用于从这些菌株中提取的肽馏分。所建立的方法比使用常规高效液相色谱和基质辅助激光解吸电离飞行时间质谱的传统方法更具优势,因为可以获得更多的结构信息,并且使用该方法更容易将微囊藻毒素与其他肽区分开来。通过该方法还可以检测到少量的其他肽。所建立的方法将有助于研究编码肽合成酶的基因与次生代谢肽之间的关系。