Mohan Gopi, Thipparamalai Thangappanpillai Ajith Kumar, Ramasamy Balagurunathan
Centre for Marine Living Resources & Ecology (MoES), Field Research Station, Agatti Island, 682 553 Lakshadweep U. T., India; CAS in Marine Biology, Faculty of Marine Sciences, Annamalai University, Parangipettai, 608 502 Tamil Nadu, India.
CAS in Marine Biology, Faculty of Marine Sciences, Annamalai University, Parangipettai, 608 502 Tamil Nadu, India; National Bureau of Fish Genetic Resources, Indian Council for Agricultural Research, Lucknow, UP, India.
Biotechnol Rep (Amst). 2016 Jun 8;11:44-52. doi: 10.1016/j.btre.2016.06.001. eCollection 2016 Sep.
Twenty-one species of sponges were recorded under the class of Demospongiae and Calcareous sponges of which 19 species were new to Agatti reef. A total of 113 Sponge endosymbiotic bacterial strains were isolated from twenty-one species of sponges and screened for antimicrobial activity. Five bacterial strains of sponge endosymbiotic bacteria (SEB) namely SEB32, SEB33, SEB36, SEB43 and SEB51 showed antimicrobial activity against virulent marine fish pathogens such as , , , , sp., sp., and . The secondary metabolites produced by SEB32 from sponge (Montagu, 1818) [48] was selected with broad range of antibacterial activity and subjected for production, characterization by series of chromatography techniques and spectroscopic methods. Based on the results of FT-IR and mass spectrometry, the active molecule was tentatively predicted as "Pyrrol" and the structure is Pyrrolo[1,2]pyrazine-1,4-dione, hexahydro- with molecular formula of C7H10N2O2. The LC of active molecule was 31 μg/ml and molecular weight of the metabolites was 154. The potential strain SEB32 was identified by gene sequence (GenBank Accession number JX985748) and identified as sp. from GenBank database.
在寻常海绵纲和钙质海绵纲下记录了21种海绵,其中19种对阿加蒂珊瑚礁来说是新物种。从21种海绵中总共分离出113株海绵共生细菌菌株,并对其进行抗菌活性筛选。5株海绵共生细菌(SEB)菌株,即SEB32、SEB33、SEB36、SEB43和SEB51,对 、 、 、 、 属、 属、 和 等剧毒海洋鱼类病原体表现出抗菌活性。从海绵 (蒙塔古,1818年)[48]中分离出的SEB32产生的次生代谢产物具有广泛的抗菌活性,被选出来进行生产,并通过一系列色谱技术和光谱方法进行表征。根据傅里叶变换红外光谱(FT-IR)和质谱结果,活性分子初步预测为“吡咯”,其结构为六氢吡咯并[1,2]吡嗪-1,4-二酮,分子式为C7H10N2O2。活性分子的最低抑菌浓度(LC)为31μg/ml,代谢产物的分子量为154。通过基因序列(GenBank登录号JX985748)鉴定了潜在菌株SEB32,并从GenBank数据库中鉴定为 属。