Haygood M G, Cohn D H
Gene. 1986;45(2):203-9. doi: 10.1016/0378-1119(86)90255-6.
Light organs of anomalopid (flashlight) fish contain luminous bacteroids that have never been cultured and, consequently, have been difficult to study. We have characterized the luciferase (lux) region of DNA extracted from light organs of the Caribbean flashlight fish Kryptophanaron alfredi by hybridization of cloned Vibrio harveyi lux genes to restriction-endonuclease-digested, light organ DNA. Comparison of the hybridization pattern of light organ DNA with that of DNA of a putative symbiotic isolate provides a method for identifying the authentic luminous symbiont regardless of its luminescence, and was used to reject one such isolate. Light organ DNA was further used to construct a cosmid clone bank and the luciferase genes were isolated. Unlike other bacterial luciferase genes, the genes were not expressed in Escherichia coli. When placed under the control of the E. coli trp promoter, the genes were transcribed but no luciferase was detected, suggesting a posttranscriptional block to expression.
异鳍躄鱼(手电筒鱼)的发光器官含有从未培养过的发光细菌类菌体,因此很难进行研究。我们通过将克隆的哈维氏弧菌lux基因与经限制性内切酶消化的发光器官DNA杂交,对从加勒比海手电筒鱼(Kryptophanaron alfredi)的发光器官中提取的DNA的荧光素酶(lux)区域进行了表征。将发光器官DNA的杂交模式与假定的共生分离株的DNA的杂交模式进行比较,提供了一种识别真正发光共生体的方法,而不论其发光情况如何,并用于排除一种这样的分离株。发光器官DNA进一步用于构建黏粒克隆文库,并分离出荧光素酶基因。与其他细菌荧光素酶基因不同,这些基因在大肠杆菌中不表达。当置于大肠杆菌trp启动子的控制下时,这些基因被转录,但未检测到荧光素酶,这表明存在转录后表达障碍。