Zebrowska Joanna, Zolnierkiewicz Olga, Skowron Marta A, Zylicz-Stachula Agnieszka, Jezewska-Frackowiak Joanna, Skowron Piotr M
Department of Molecular Biotechnology, Institute for Environment and Human Health Protection, Faculty of Chemistry, University of Gdansk, Wita Stwosza 63, 80-308 Gdansk, Poland.
J Biosci. 2016 Mar;41(1):27-38. doi: 10.1007/s12038-016-9595-z.
Screening of extreme environments in search for novel microorganisms may lead to the discovery of robust enzymes with either new substrate specificities or thermostable equivalents of those already found in mesophiles, better suited for biotechnology applications. Isolates from Iceland geysers' biofilms, exposed to a broad range of temperatures, from ambient to close to water boiling point, were analysed for the presence of DNA-interacting proteins, including restriction endonucleases (REases). GeoICI, a member of atypical Type IIS REases, is the most thermostable isoschizomer of the prototype BbvI, recognizing/cleaving 5'-GCAGC(N8/12)-3'DNA sequences. As opposed to the unstable prototype, which cleaves DNA at 30°C, GeoICI is highly active at elevated temperatures, up to 73°C and over a very wide salt concentration range. Recognition/cleavage sites were determined by: (i) digestion of plasmid and bacteriophage lambda DNA (Λ); (ii) cleavage of custom PCR substrates, (iii) run-off sequencing of GeoICI cleavage products and (iv) shotgun cloning and sequencing of Λ DNA fragmented with GeoICI. Geobacillus sp. genomic DNA was PCR-screened for the presence of other specialized REases-MTases and as a result, another putative REase- MTase, GeoICII, related to the Thermus sp. family of bifunctional REases-methyltransferases (MTases) was detected.
在极端环境中筛选新型微生物可能会发现具有新底物特异性的强大酶,或者是嗜温菌中已发现的酶的耐热等效物,更适合生物技术应用。对来自冰岛间歇泉生物膜的分离物进行了分析,这些分离物暴露于从环境温度到接近水沸点的广泛温度范围内,以检测与DNA相互作用的蛋白质的存在,包括限制性内切核酸酶(REases)。GeoICI是非典型IIS型REases的成员,是原型BbvI最耐热的同裂酶,识别/切割5'-GCAGC(N8/12)-3' DNA序列。与在30°C切割DNA的不稳定原型不同,GeoICI在高温下(高达73°C)以及非常宽的盐浓度范围内都具有高活性。通过以下方法确定识别/切割位点:(i) 消化质粒和噬菌体λ DNA(Λ);(ii) 切割定制的PCR底物;(iii) 对GeoICI切割产物进行连续测序;(iv) 对用GeoICI切割的Λ DNA进行鸟枪法克隆和测序。对嗜热栖热菌属基因组DNA进行PCR筛选,以检测其他特殊的REases-MTases的存在,结果检测到另一种推定的REase-MTase,即与嗜热栖热菌属双功能REases-甲基转移酶(MTases)家族相关的GeoICII。