A Novel and Efficient Phthalate Hydrolase from Acinetobacter sp. LUNF3: Molecular Cloning, Characterization and Catalytic Mechanism

被引:6
作者
Fan, Shuanghu [1 ,2 ,3 ]
Guo, Jingjing [4 ]
Han, Shaoyan [1 ]
Du, Haina [1 ]
Wang, Zimeng [1 ]
Fu, Yajuan [1 ,3 ]
Han, Hui [1 ,3 ]
Hou, Xiaoqiang [1 ,3 ]
Wang, Weixuan [5 ,6 ]
机构
[1] Langfang Normal Univ, Coll Life Sci, Langfang 065000, Peoples R China
[2] Chinese Acad Agr Sci, Inst Agr Resources & Reg Planning, Beijing 100081, Peoples R China
[3] Tech Innovat Ctr Utilizat Edible & Med Fungi Hebei, Langfang 065000, Peoples R China
[4] Langfang Normal Univ, Sch Chem & Mat Sci, Langfang 065000, Peoples R China
[5] Chinese Acad Agr Sci, Biotechnol Res Inst, Beijing 100081, Peoples R China
[6] Chinese Acad Agr Sci, Natl Nanfan Res Inst Sanya, Sanya 572024, Peoples R China
来源
MOLECULES | 2023年 / 28卷 / 18期
关键词
Acinetobacter; biodegradation; genome sequencing; HSL family hydrolase; site-directed mutagenesis; N-BUTYL PHTHALATE; DI-(2-ETHYLHEXYL) PHTHALATE; BIODEGRADATION PATHWAY; DEGRADATION; ESTERS; DEHP; GENE; EXPRESSION; SEQUENCE;
D O I
10.3390/molecules28186738
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phthalic acid esters (PAEs), which are widespread environmental contaminants, can be efficiently biodegraded, mediated by enzymes such as hydrolases. Despite great advances in the characterization of PAE hydrolases, which are the most important enzymes in the process of PAE degradation, their molecular catalytic mechanism has rarely been systematically investigated. Acinetobacter sp. LUNF3, which was isolated from contaminated soil in this study, demonstrated excellent PAE degradation at 30 degree celsius and pH 5.0-11.0. After sequencing and annotating the complete genome, the gene dphAN1, encoding a novel putative PAE hydrolase, was identified with the conserved motifs catalytic triad (Ser(201)-Asp(295)-His(325)) and oxyanion hole (H(127)GGG(130)). DphAN1 can hydrolyze DEP (diethyl phthalate), DBP (dibutyl phthalate) and BBP (benzyl butyl phthalate). The high activity of DphAN1 was observed under a wide range of temperature (10-40 degree celsius) and pH (6.0-9.0). Moreover, the metal ions (Fe2+, Mn2+, Cr2+ and Fe3+) and surfactant TritonX-100 significantly activated DphAN1, indicating a high adaptability and tolerance of DphAN1 to these chemicals. Molecular docking revealed the catalytic triad, oxyanion hole and other residues involved in binding DBP. The mutation of these residues reduced the activity of DphAN1, confirming their interaction with DBP. These results shed light on the catalytic mechanism of DphAN1 and may contribute to protein structural modification to improve catalytic efficiency in environment remediation.
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页数:19
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