Department of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Korea.
Division of Polar Life Science, Korea Polar Research Institute, KIOST, Incheon 406-840, Korea.
Mar Drugs. 2017 Oct 18;15(10):318. doi: 10.3390/md15100318.
Antifreeze proteins (AFPs) protecting the cells against freezing are produced in response to extremely low temperatures in diverse psychrophilic organisms, and they are encoded by multiple gene families. The AFP of Antarctic marine diatom is reported in our previous research, but like other microalgae, was considered to probably have additional genes coding AFPs. In this paper, we reported the cloning and characterization of additional AFP gene from (). protein is 74.6% identical to the previously reported Cn-AFP. The promoter sequence of contains environmental stress responsive elements for cold, thermal, and high light conditions. transcription levels increased dramatically when cells were exposed to freezing (-20 °C), thermal (10 °C), or high light (600 μmol photon m s) stresses. The thermal hysteresis (TH) activity of recombinant Cn-isoAFP was 0.8 °C at a protein concentration of 5 mg/mL. Results from homology modeling and TH activity analysis of site-directed mutant proteins elucidated AFP mechanism to be a result of flatness of B-face maintained via hydrophobic interactions.
抗冻蛋白(AFPs)可保护细胞免受冷冻损伤,它们在各种嗜冷生物中响应极低的温度而产生,由多个基因家族编码。我们之前的研究报道了南极海洋硅藻的 AFP,但与其他微藻一样,人们认为它可能还有其他编码 AFP 的基因。在本文中,我们报道了来自 ()的额外 AFP 基因的克隆和特性。该蛋白与之前报道的 Cn-AFP 有 74.6%的同一性。 的启动子序列包含了对冷、热和高光条件的环境应激响应元件。当细胞受到冷冻(-20°C)、热(10°C)或高光(600 μmol 光子 m s)胁迫时, 转录水平显著增加。重组 Cn-isoAFP 的热滞(TH)活性在 5mg/mL 蛋白浓度下为 0.8°C。同源建模和定点突变蛋白 TH 活性分析的结果阐明了 AFP 的作用机制是通过疏水性相互作用维持 B 面的平坦度。