Gao Peng, Xi Lijun, Piao Yuhua, Ruan Jisheng, Huang Ying
State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Wei Sheng Wu Xue Bao. 2009 Oct;49(10):1367-73.
To compare the halometabolite producing capability between actinomycetes of earth origin and marine origin, based on genetic screening of the 1,5-dihydroflavin adenine dinucleotide (FADH2-dependent) halogenase gene.
We used 141 actinomycete isolates that were dereplicated by phenotype, 70 of earth origin and 71 of marine origin, and obtained halogenase gene fragments from them by PCR screening. We then sequenced the PCR products and analyzed corresponding amino acid sequences phylogenetically. We made further comparison of the halogenase sequences between actinomycetes of different origins, and between marine-origin streptomycetes and marine-origin Micromonospora isolates. In addition, we detected polyketide synthase (PKS) and non-ribosomal peptide synthetase (NRPS) genes by PCR in the halogenase gene-positive isolates.
We observed higher occurrence of the halogenase gene in marine-origin actinomycetes (36.6%) than in earth-origin actinomycetes (14.3%), and in marine-origin streptomycetes (69.0%) than in marine-origin Micromonospora isolates (14.3%). Most (86.1%) of the halogenase gene-positive isolates contained PKS and/or NRPS genes. Moreover, the halogenase sequences of marine-origin isolates differed largely from the known ones, and clustered into a couple of distinct clades in the phylogenetic tree. In addition, we found greater diversity of the halogenase genes in marine-origin Micromonospora isolates than in marine-origin streptomycetes.
Based on the results of this study, we propose that actinomycetes, especially streptomycetes, from marine habitat could serve as a good source for new bioactive halometabolite discovery in the future.
基于对1,5 - 二氢黄素腺嘌呤二核苷酸(依赖FADH2)卤化酶基因的遗传筛选,比较陆生放线菌和海洋放线菌产生卤代代谢产物的能力。
我们使用了141株经表型去重复的放线菌分离株,其中70株来自陆地,71株来自海洋,通过PCR筛选从它们中获得卤化酶基因片段。然后对PCR产物进行测序,并对相应的氨基酸序列进行系统发育分析。我们进一步比较了不同来源放线菌之间以及海洋来源链霉菌和海洋来源小单孢菌分离株之间的卤化酶序列。此外,我们通过PCR在卤化酶基因阳性分离株中检测聚酮合酶(PKS)和非核糖体肽合成酶(NRPS)基因。
我们观察到海洋来源放线菌(36.6%)中卤化酶基因的出现频率高于陆地来源放线菌(14.3%),海洋来源链霉菌(69.0%)中卤化酶基因的出现频率高于海洋来源小单孢菌分离株(14.3%)。大多数(86.1%)卤化酶基因阳性分离株含有PKS和/或NRPS基因。此外,海洋来源分离株的卤化酶序列与已知序列有很大差异,并在系统发育树中聚为几个不同的分支。此外,我们发现海洋来源小单孢菌分离株中卤化酶基因的多样性高于海洋来源链霉菌。
基于本研究结果,我们提出海洋生境中的放线菌,尤其是链霉菌,未来可作为发现新型生物活性卤代代谢产物的良好来源。