Brzostowicz P C, Gibson K L, Thomas S M, Blasko M S, Rouvière P E
E. I. DuPont de Nemours Co., Central Research and Development, Wilmington, Delaware 19800-0328, USA.
J Bacteriol. 2000 Aug;182(15):4241-8. doi: 10.1128/JB.182.15.4241-4248.2000.
The technique of mRNA differential display was used to identify simultaneously two metabolic genes involved in the degradation of cyclohexanone in a new halotolerant Brevibacterium environmental isolate. In a strategy based only on the knowledge that cyclohexanone oxidation was inducible in this strain, the mRNA population of cells exposed to cyclohexanone was compared to that of control cells using reverse transcription-PCR reactions primed with a collection of 81 arbitrary oligonucleotides. Three DNA fragments encoding segments of flavin monooxygenases were isolated with this technique, leading to the identification of the genes of two distinct cyclohexanone monooxygenases, the enzymes responsible for the oxidation of cyclohexanone. Each monooxygenase was expressed in Escherichia coli and characterized. This work validates the application of mRNA differential display for the discovery of new microbial metabolic genes.
利用mRNA差异显示技术,在一株新的耐盐短杆菌环境分离株中同时鉴定出两个参与环己酮降解的代谢基因。在仅基于环己酮氧化在该菌株中可诱导这一认识的策略中,使用由81种任意寡核苷酸组成的引物集合进行逆转录 - PCR反应,将暴露于环己酮的细胞的mRNA群体与对照细胞的mRNA群体进行比较。用该技术分离出三个编码黄素单加氧酶片段的DNA片段,从而鉴定出两种不同的环己酮单加氧酶的基因,这两种酶负责环己酮的氧化。每种单加氧酶都在大肠杆菌中表达并进行了表征。这项工作验证了mRNA差异显示在发现新的微生物代谢基因方面的应用。