Soriano-Maldonado Pablo, Andújar-Sánchez Montserrat, Clemente-Jiménez Josefa María, Rodríguez-Vico Felipe, Las Heras-Vázquez Francisco Javier, Martínez-Rodríguez Sergio
Dpto. Química y Física, Universidad de Almería, Campus de Excelencia Internacional Agroalimentario, ceiA3, Edificio CITE I, Carretera de Sacramento s/n., 04120, La Cañada de San Urbano, Almería, Spain.
Mol Biotechnol. 2015 May;57(5):454-65. doi: 10.1007/s12033-015-9839-4.
N-Succinyl-amino acid racemase (NSAAR), long referred to as N-acyl- or N-acetyl-amino acid racemase, is an enolase superfamily member whose biotechnological potential was discovered decades ago, due to its use in the industrial dynamic kinetic resolution methodology first known as "Acylase Process". In previous works, an extended and enhanced substrate spectrum of the NSAAR from Geobacillus kaustophilus CECT4264 toward different N-substituted amino acids was reported. In this work, we describe the cloning, purification, and characterization of the NSAAR from Geobacillus stearothermophilus CECT49 (GstNSAAR). The enzyme has been extensively characterized, showing a higher preference toward N-formyl-amino acids than to N-acetyl-amino acids, thus confirming that the use of the former substrates is more appropriate for a biotechnological application of the enzyme. The enzyme showed an apparent thermal denaturation midpoint of 77.0 ± 0.1 °C and an apparent molecular mass of 184 ± 5 kDa, suggesting a tetrameric species. Optimal parameters for the enzyme activity were pH 8.0 and 55-65 °C, with Co(2+) as the most effective cofactor. Mutagenesis and binding experiments confirmed K166, D191, E216, D241, and K265 as key residues in the activity of GstNSAAR, but not indispensable for substrate binding.
N-琥珀酰氨基酸消旋酶(NSAAR),长期以来被称为N-酰基或N-乙酰基氨基酸消旋酶,是烯醇酶超家族成员,几十年前就发现了其生物技术潜力,这是由于它在最初被称为“酰基转移酶法”的工业动态动力学拆分方法中的应用。在先前的研究中,已报道嗜热栖热放线菌CECT4264的NSAAR对不同N-取代氨基酸具有更广泛且增强的底物谱。在这项工作中,我们描述了嗜热栖热放线菌CECT49的NSAAR(GstNSAAR)的克隆、纯化和特性。该酶已得到广泛表征,结果表明它对N-甲酰基氨基酸的偏好高于N-乙酰基氨基酸,从而证实使用前一种底物更适合该酶的生物技术应用。该酶的表观热变性中点为77.0±0.1℃,表观分子量为184±5 kDa,表明为四聚体形式。该酶活性的最佳参数为pH 8.0和55 - 65℃,Co(2+)是最有效的辅因子。诱变和结合实验证实K166、D191、E216、D241和K265是GstNSAAR活性中的关键残基,但对于底物结合并非不可或缺。