Misawa N, Satomi Y, Kondo K, Yokoyama A, Kajiwara S, Saito T, Ohtani T, Miki W
Central Laboratories for Key Technology, Kirin Brewery Co., Ltd., Kanagawa, Japan.
J Bacteriol. 1995 Nov;177(22):6575-84. doi: 10.1128/jb.177.22.6575-6584.1995.
A carotenoid biosynthesis gene cluster for the production of astaxanthin was isolated from the marine bacterium Agrobacterium aurantiacum. This cluster contained five carotenogenic genes with the same orientation, which were designated crtW, crtZ, crtY, crtI, and crtB. The stop codons of individual crt genes except for crtB overlapped the start codons of the following crt genes. Escherichia coli transformants carrying the Erwinia uredovora carotenoid biosynthesis genes provide suitable substrates for carotenoid biosynthesis. The functions of the five crt genes of A. aurantiacum were determined through chromatographic and spectroscopic analyses of the pigments accumulated in some E. coli transformants carrying various combinations of the E. uredovora and A. aurantiacum carotenogenic genes. As a result, the astaxanthin biosynthetic pathway is proposed for the first time at the level of the biosynthesis genes. The crtW and crtZ gene products, which mediated the oxygenation reactions from beta-carotene to astaxanthin, were found to have low substrate specificity. This allowed the production of many presumed intermediates of astaxanthin, i.e., adonixanthin, phoenicoxanthin (adonirubin), canthaxanthin, 3'-hydroxyechinenone, and 3-hydroxyechinenone.
从海洋细菌橙色土壤杆菌中分离出一个用于生产虾青素的类胡萝卜素生物合成基因簇。该基因簇包含五个同向的类胡萝卜素生成基因,分别命名为crtW、crtZ、crtY、crtI和crtB。除crtB外,各个crt基因的终止密码子与后续crt基因的起始密码子重叠。携带丁香假单胞菌类胡萝卜素生物合成基因的大肠杆菌转化体为类胡萝卜素生物合成提供了合适的底物。通过对携带丁香假单胞菌和橙色土壤杆菌类胡萝卜素生成基因不同组合的一些大肠杆菌转化体中积累的色素进行色谱和光谱分析,确定了橙色土壤杆菌五个crt基因的功能。结果,首次在生物合成基因水平上提出了虾青素生物合成途径。发现介导从β-胡萝卜素到虾青素氧化反应的crtW和crtZ基因产物具有较低的底物特异性。这使得能够产生许多推测的虾青素中间体,即adonixanthin、phoenicoxanthin(adonirubin)、角黄素、3'-羟基海胆酮和3-羟基海胆酮。