耐高温的A类酸性磷酸酶,在广泛的pH范围和不同的底物中都有活性。

IF 5.2 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Protein Science Pub Date : 2025-09-01 DOI:10.1002/pro.70244
Maria-Isabel Recio, José A Gavira, Jesús de La Torre, Mario Cano-Muñoz, Sergio Martínez-Rodriguez, Abdelali Daddaoua, Estrella Duque, Juan L Ramos
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引用次数: 0

摘要

M2-32是一种非特异性酸性磷酸酶,具有在广泛pH范围(3.5-8.5)内发挥作用的罕见能力。使用SWISS-PROT Prf Profiles进行分析,将其归类为a类酸性磷酸酶(Z-score: 78.97),与PhoC和PhoN等酶具有50%-60%的序列相似性。为了详细表征,将编码M2-32的基因克隆到pET28(b)载体中,在大肠杆菌BL21 (DE3)中过表达,随后纯化。虽然M2-32的单体形式分子量为~28 kDa,但粒径排除色谱、动态光散射和沉降研究显示其在溶液中为二聚体形式。使用对硝基苯磷酸、4-甲基伞草酰磷酸、3′和5′-单磷酸腺苷进行酶分析,在30°和50°C的pH范围为4.0-8.0范围内显示出强大的活性。差示扫描荧光法显示,展开温度接近47℃;但在80℃热变性后,酶发生了再折叠。我们使用alphafold2引导的截断模型通过分子替换确定了M2-32的x射线晶体结构,达到了2.2 Å的分辨率。这种蛋白质结晶为二聚体的二聚体。每个单体(残基38-274)采用由14个螺旋和两个二硫键组成的全螺旋折叠。与单磷酸腺苷的对接研究,结合定点突变,鉴定出His174, Arg207, His213, Asp217是关键的催化残基,Tyr136和Ser172可能参与底物识别。这些位置的突变导致超过90%的酶活性丧失,突出了它们的功能意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thermotolerant class A acid phosphatase active across broad pH range and diverse substrates.

M2-32 is a non-specific acid phosphatase with a rare ability to function across a broad pH range (3.5-8.5). Analysis using SWISS-PROT Prf Profiles classifies it as a class A acid phosphatase (Z-score: 78.97), sharing 50%-60% sequence similarity with enzymes such as PhoC and PhoN. For detailed characterization, the gene encoding M2-32 was cloned into the pET28(b) vector, overexpressed in Escherichia coli BL21 (DE3), and subsequently purified. Although the monomeric form of M2-32 has a molecular weight of ~28 kDa, size exclusion chromatography, dynamic light scattering, and sedimentation studies revealed a dimeric form in solution. Enzymatic assays using p-nitrophenyl phosphate, 4-methylumbelliferyl phosphate, 3'-and 5'-adenosine monophosphate demonstrated robust activity over a pH range of 4.0-8.0 at both 30 and 50°C. Differential scanning fluorimetry indicated an unfolding temperature close to 47°C; however, the enzyme refolded after heat denaturation at 80°C. We have determined the x-ray crystal structure of M2-32 by molecular replacement using an AlphaFold2-guided truncated model, achieving a resolution of 2.2 Å. The protein crystallized as a dimer-of-dimers. Each monomer (residues 38-274) adopts an all-alpha-helical fold composed of 14 helices and two disulfide bonds. Docking studies with adenosine monophosphates, combined with site-directed mutagenesis, identified His174, Arg207, His213, Asp217 as critical catalytic residues, and Tyr136 and Ser172 probably involved in substrate recognition. Mutations at these positions resulted in over 90% loss of enzymatic activity, highlighting their functional significance.

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来源期刊
Protein Science
Protein Science 生物-生化与分子生物学
CiteScore
12.40
自引率
1.20%
发文量
246
审稿时长
1 months
期刊介绍: Protein Science, the flagship journal of The Protein Society, is a publication that focuses on advancing fundamental knowledge in the field of protein molecules. The journal welcomes original reports and review articles that contribute to our understanding of protein function, structure, folding, design, and evolution. Additionally, Protein Science encourages papers that explore the applications of protein science in various areas such as therapeutics, protein-based biomaterials, bionanotechnology, synthetic biology, and bioelectronics. The journal accepts manuscript submissions in any suitable format for review, with the requirement of converting the manuscript to journal-style format only upon acceptance for publication. Protein Science is indexed and abstracted in numerous databases, including the Agricultural & Environmental Science Database (ProQuest), Biological Science Database (ProQuest), CAS: Chemical Abstracts Service (ACS), Embase (Elsevier), Health & Medical Collection (ProQuest), Health Research Premium Collection (ProQuest), Materials Science & Engineering Database (ProQuest), MEDLINE/PubMed (NLM), Natural Science Collection (ProQuest), and SciTech Premium Collection (ProQuest).
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