(19)
(11) EP 2 390 315 A8

(12) CORRECTED EUROPEAN PATENT APPLICATION
Note: Bibliography reflects the latest situation

(15) Correction information:
Corrected version no 1 (W1 A1)

(48) Corrigendum issued on:
09.05.2012 Bulletin 2012/19

(88) Date of publication A3:
30.11.2011 Bulletin 2011/48

(43) Date of publication:
30.11.2011 Bulletin 2011/48

(21) Application number: 11075099.9

(22) Date of filing: 14.07.2008
(51) International Patent Classification (IPC): 
C12N 9/22(2006.01)
(84) Designated Contracting States:
AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR

(30) Priority: 12.07.2007 US 959203

(62) Application number of the earlier application in accordance with Art. 76 EPC:
08796186.8 / 2167655

(71) Applicant: NEW ENGLAND BIOLABS, INC.
Ipswich, MA 01938-2723 (US)

(72) Inventors:
  • Zhu, Zhenyu
    Beverly, MA 01915 (US)
  • Blanchard, Aine
    Wakefield, MA 01880 (US)
  • Xu, Shuang-Yong
    Lexington, MA 02420 (US)
  • Guan, Shengxi
    Ipswich, MA 01938 (US)
  • Wei, Hua
    New Brunswick, NJ 08901 (US)
  • Zhang, Penghua
    Lexington, MA 02421 (US)
  • Sun, Dapeng
    Arlington, MA 02474 (US)
  • Chan, Siu-hong
    Ipswich, MA 01938 (US)

(74) Representative: Froud, Clive 
Clive Froud & Co Limited 7 Hurst Close Tenterden
Kent TN30 6UG
Kent TN30 6UG (GB)

 
Remarks:
This application was filed on 24-05-2011 as a divisional application to the application mentioned under INID code 62.
 


(54) High fidelity restriction endonucleases


(57) Inter alia, a composition characterized in that it comprises: a restriction endonuclease enzyme having at least one artificially introduced mutation and an overall fidelity index (FI) improvement factor of at least 2, the restriction endonuclease being capable of cleaving a substrate with at least a similar cleavage activity to that of the restriction endonuclease absent the artificially introduced mutation, in a predetermined buffer, wherein the artificially introduced mutation is the product of at least one of a targeted mutation, saturation mutagenesis, or a mutation introduced through a PCR amplification procedure, and wherein the restriction endonuclease absent the artificially introduced mutation is PvuII and the artificially introduced mutation is selected from: T46A; T46H; T46K; T46Y; and T46G is disclosed.