从两栖藻中提取的多功能催化血红蛋白:分离、分类鉴定、蛋白质提取、纯化和表征的方法。

IF 2.3 Q3 BIOCHEMICAL RESEARCH METHODS Methods and Protocols Pub Date : 2024-12-11 DOI:10.3390/mps7060100
Anna L Husted, Victoria R Sutton, Lauren A Presnar, R Kevin Blackburn, Joseph L Staton, Stephen A Borgianini, Edward L D'Antonio
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引用次数: 0

摘要

来自terebellid polychaete Amphitrite ornata的多功能催化血红蛋白,也被称为脱盐过氧化物酶(AoDHP),除了具有典型的氧转运功能外,还具有四种观察到的涉及底物氧化的活性。AoDHP的多功能能力目前是一种罕见的观察,并且如何从大型底栖动物中鉴定新的脱盐过氧化物酶存在限制。为了发现更多的动物dhp候选者,我们设计了一种简便的方法,将视觉和分子分类方法并行进行准确的分类鉴定。传统的视觉分类物种鉴定是一项非常困难和耗时的任务,至少对于a . ornata或其他海洋蠕虫来说,因为存在大量的多样性,而且这种方法仅限于成虫标本。本文旨在描述一种利用DNA条形码技术,通过对其线粒体细胞色素c氧化酶亚基I基因的评估,简化了a . ornata分类鉴定的方法。此外,我们还利用全虫标本提取纯化了AoDHP,并进行了h2o2依赖性过氧化物酶对底物2,4,6-三氯酚的活性测定。AoDHP同工酶A也以重组蛋白的形式在大肠杆菌中过表达,并将其过氧化物酶活性参数与天然来源的AoDHP进行比较。活性分析评估表明,所有Michaelis-Menten参数评估密切相关。我们的结论是,本文描述的方法展示了一种简化的方法来识别多毛藻a . ornata,可以被非专业人员采用,并且整个过程预计将有助于从其他海洋无脊椎动物中发现新的脱盐过氧化物酶。
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The Multifunctional Catalytic Hemoglobin from Amphitrite ornata: Protocols on Isolation, Taxonomic Identification, Protein Extraction, Purification, and Characterization.

The multifunctional catalytic hemoglobin from the terebellid polychaete Amphitrite ornata, also named dehaloperoxidase (AoDHP), utilizes the typical oxygen transport function in addition to four observed activities involved in substrate oxidation. The multifunctional ability of AoDHP is presently a rare observation, and there exists a limitation for how novel dehaloperoxidases can be identified from macrobenthic infauna. In order to discover more infaunal DHP-bearing candidates, we have devised a facilitated method for an accurate taxonomic identification that places visual and molecular taxonomic approaches in parallel. Traditional visual taxonomic species identification by the non-specialist, at least for A. ornata or even for other marine worms, is a very difficult and time-consuming task since a large diversity is present and the method is restricted to adult worm specimens. The work herein aimed to describe a method that simplifies the taxonomic identification of A. ornata in particular through the assessment of its mitochondrial cytochrome c oxidase subunit I gene by employing the DNA barcoding technique. Furthermore, whole-worm specimens of A. ornata were used to extract and purify AoDHP followed by an H2O2-dependent peroxidase activity assay evaluation against substrate 2,4,6-trichlorophenol. AoDHP isoenzyme A was also overexpressed as the recombinant protein in Escherichia coli, and its peroxidase activity parameters were compared to AoDHP from the natural source. The activity assay assessment indicated a tight correlation for all Michaelis-Menten parameters evaluated. We conclude that the method described herein exhibits a streamlined approach to identify the polychaete A. ornata, which can be adopted by the non-specialist, and the full procedure is predicted to facilitate the discovery of novel dehaloperoxidases from other marine invertebrates.

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来源期刊
Methods and Protocols
Methods and Protocols Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (miscellaneous)
CiteScore
3.60
自引率
0.00%
发文量
85
审稿时长
8 weeks
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