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公开(公告)号:US20170096652A1
公开(公告)日:2017-04-06
申请号:US15378035
申请日:2016-12-13
Applicant: Zhejiang University
Inventor: Yuejin Hua , Yunguang Wang , Liangyan Wang
IPC: C12N9/52
CPC classification number: C12N9/52 , C12Y304/00 , G10H1/0066 , G10H1/0551 , G10H1/18 , G10H2220/096 , G10H2220/121 , G10H2220/241 , G10H2220/275 , G10H2220/461
Abstract: The present invention relates to a polypeptide having protease activity comprising a zinc finger protease domain, a helix-turn-helix domain and a GAF domain. The core protein sequence of the protease is shown as SEQ ID NO: 1. The invention also relates to optimized reaction conditions for the protease and methods of increasing the protease activity.
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公开(公告)号:US10316310B2
公开(公告)日:2019-06-11
申请号:US15378035
申请日:2016-12-13
Applicant: Zhejiang University
Inventor: Yuejin Hua , Yunguang Wang , Liangyan Wang
Abstract: The present invention relates to a polypeptide having protease activity comprising a zinc finger protease domain, a helix-turn-helix domain and a GAF domain. The core protein sequence of the protease is shown as SEQ ID NO: 1. The invention also relates to optimized reaction conditions for the protease and methods of increasing the protease activity.
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公开(公告)号:US20230183662A1
公开(公告)日:2023-06-15
申请号:US17552076
申请日:2021-12-15
Applicant: Zhejiang University
Inventor: Yuejin Hua , Shengjie Li , Liangyan Wang , Jianling Cai , Xiaoting Hua
IPC: C12N9/10
CPC classification number: C12N9/1007 , C12Y201/01037
Abstract: A DNA methyltransferase is derived from Deinococcus radiodurans and has a typical conservative structural domain of DNA methyltransferase. The DNA methyltransferase includes: an AdoMet binding region containing a “FxGxG” conservative sequence, a target sequence recognition region and a catalytic region containing a “TSPPY” conservative sequence sequentially from N-terminal to C-terminal; and belongs to α-type DNA methyltransferase category. The recognized substrate DNA conservative sequence is 5′-CCGCGG-3′, a methylation modified position is N4 site of second cytosine to generate a 4mC type modified base, and an optimum temperature for methylated reaction is in a range of 25-37° C. The DNA methyltransferase can specific-recognize the conservative motif of “CCGCGG” and methylate the N4 site of the second cytosine to produce the 4mC modified base, which is a N4-Cytosine DNA methyltransferase.
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公开(公告)号:US11697805B2
公开(公告)日:2023-07-11
申请号:US17229653
申请日:2021-04-13
Applicant: Zhejiang University
Inventor: Yuejin Hua , Xingru Zhou , Liangyan Wang , Xuanyi Chen
IPC: C12N9/12 , C07K14/195 , C12Q1/6844
CPC classification number: C12N9/1252 , C07K14/195 , C12Q1/6844
Abstract: The disclosure provides a high-fidelity polymerase with preference for gapped DNA and use thereof. The Klenow fragment (KlenDr) derived from Deinococcus radiodurans DNA polymerase I, which has the high-fidelity polymerization characteristics, is independent of 3′-5′ proofreading exonuclease activity, has the preference for binding gapped DNA, and is different from the existing commercial high-fidelity polymerase. Due to the specific affinity of KlenDr to gapped DNA substrate, the 3′ end of the forward primer will not be cut off, and the downstream nucleotide chain is rarely replaced.
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