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[基于Phi29 DNA聚合酶的新型酶的挖掘与表征]

[Mining and characterization of new enzymes based on Phi29 DNA polymerase].

作者信息

Hao Mengyao, Hu Lingling, Han Minghao, Li Congyu, Chang Hong, Luo Jianmei, Jiang Huifeng

机构信息

School of Biological Engineering, Tianjin University of Science & Technology, Tianjin 300457, China.

Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2025 Jan 25;41(1):427-436. doi: 10.13345/j.cjb.240222.

Abstract

In recent years, the bacteriophage Φ29 (Phi29) DNA polymerase has garnered increasing attention due to its high-fidelity amplification capacity at constant temperatures. To advance the industrial application of this type of isothermal polymerases, this study mined and characterized new enzymes from the microbial metagenome based on the known Phi29 DNA polymerase sequence. The results revealed that a new enzyme, Php29 DNA polymerase, was identified in the microbial metagenome with plants as the hosts. This enzyme exhibited higher strand displacement activity, with a 59.5% similarity to bacteriophage Φ29. Experimental validation demonstrated that the enzyme had 3'→5' exonuclease activity, and its amplification products can serve as substrates for further catalytic reactions. The discovery and validation of Php29 DNA polymerase gives insights into the future industrial application of isothermal polymerases.

摘要

近年来,噬菌体Φ29 DNA聚合酶因其在恒温下的高保真扩增能力而受到越来越多的关注。为了推进这类等温聚合酶的工业应用,本研究基于已知的Φ29 DNA聚合酶序列,从微生物宏基因组中挖掘并鉴定了新的酶。结果显示,在以植物为宿主的微生物宏基因组中鉴定出一种新酶——Php29 DNA聚合酶。该酶表现出更高的链置换活性,与噬菌体Φ29的相似性为59.5%。实验验证表明,该酶具有3'→5'核酸外切酶活性,其扩增产物可作为进一步催化反应的底物。Php29 DNA聚合酶的发现和验证为等温聚合酶未来的工业应用提供了思路。

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