IP Library Granted Patent US 11,214,787
Granted Patent B2
US 11,214,787 · App. 16/279,547 · Granted Jan 4, 2022

Modified beta-lactamases and methods and uses related thereto

Inventors: Pertti Koski (Helsinki, FI); Ulla Airaksinen (Vantaa, FI); Katja Valimaki (Vantaa, FI)
Assignee: Synthetic Biologies, Inc.
C12N9/86A61K9/0053A61K9/4891A61K31/43A61K31/545A61K38/50A61K45/06C12Y305/02006A61K38/00
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Quick Facts
Patent No.
US 11,214,787
App. No.
16/279,547
Granted
Jan 4, 2022
Kind
B2
Abstract

The present invention relates to pharmaceuticals and modified beta-lactamases. Specifically, the invention relates to novel recombinant beta-lactamases and pharmaceutical compositions comprising the beta-lactamases. Also, the present invention relates to methods for modifying a beta-lactamase, producing the beta-lactamase and treating or preventing beta-lactam antibiotic induced adverse effects. Furthermore, the present invention relates to the beta-lactamase for use as a medicament and to the use of the beta-lactamase in the manufacture of a medicament for treating or preventing beta-lactam antibiotics induced adverse effects. Still further, the invention relates to a polynucleotide and a host cell comprising the polynucleotide.

Claims (18)

1. A composition, comprising a beta-lactamase comprising an amino acid sequence having at least 98% sequence identity with SEQ ID NO: 1 and a hydrophilic amino acid residue other than aspartic acid (D) at the position corresponding to position 276 according to Ambler classification,

wherein the hydrophilic amino acid residue is selected from asparagine (N) and glutamine (Q).

2. The composition of claim 1 , wherein the hydrophilic amino acid residue is located in an alpha helix.

3. The composition of claim 1 , wherein the beta-lactamase further comprises at least one amino acid selected from a leucine (L) at a position corresponding to position 220 and an arginine (R) at a position corresponding to position 244 according to Ambler classification.

4. The composition of claim 1 , wherein the beta-lactamase hydrolyzes a penicillin and a cephalosporin.

5. The composition of claim 4 , wherein the cephalosporin is selected from cefoperazone and ceftriaxone.

6. The composition of claim 4 , wherein the cephalosporin has been excreted into the gastrointestinal tract.

7. The composition of claim 1 , wherein the beta-lactamase comprises an amino acid sequence having at least 99% sequence identity with SEQ ID NO: 1.

8. The composition of claim 1 , wherein the beta-lactamase comprises the amino acid sequence of SEQ ID NO: 1.

9. A pharmaceutical composition comprising the composition of claim 1 .

10. A pharmaceutical composition for oral administration comprising an effective amount of a beta-lactamase comprising an amino acid sequence having at least 98% sequence identity with SEQ ID NO: 1 and a hydrophilic amino acid residue other than aspartic acid (D) at the position corresponding to position 276 according to Ambler classification,

wherein the hydrophilic amino acid residue is selected from asparagine (N) and glutamine (Q).

11. The pharmaceutical composition of claim 10 , wherein the beta-lactamase hydrolyzes a penicillin and a cephalosporin.

12. The pharmaceutical composition of claim 11 , wherein the cephalosporin is selected from cefoperazone and ceftriaxone.

13. The pharmaceutical composition of claim 11 , wherein the cephalosporin has been excreted into the gastrointestinal tract.

14. The pharmaceutical composition of claim 10 , wherein the beta-lactamase comprises an amino acid sequence having at least 99% sequence identity with SEQ ID NO: 1.

15. The pharmaceutical composition of claim 10 , wherein the beta-lactamase comprises the amino acid sequence of SEQ ID NO: 1.

16. The pharmaceutical composition of claim 10 , wherein the beta-lactamase further comprises at least one amino acid selected from a leucine (L) at a position corresponding to position 220 and an arginine (R) at a position corresponding to position 244 according to Ambler classification.

Assignments (3)
CHANGE OF NAME Recorded Apr 4, 2023
From: SYNTHETIC BIOLOGICS, INC.
To: THERIVA BIOLOGICS, INC.
Reel/Frame 063214/0229 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2020
From: KOSKI, PERTTI; AIRAKSINEN, ULLA; VALIMAKI, KATJA
To: PREV ABR LLC
Reel/Frame 054218/0796 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2020
From: PREV ABR LLC
To: SYNTHETIC BIOLOGICS, INC.
Reel/Frame 054264/0357 →
Priority Claims (1)
FI 20105572 · May 24, 2010 · national
Continuity (8)
Continuation 15661416 · Jul 27, 2017
Continuation 15138767 · Apr 26, 2016
Continuation 15054292 · Feb 26, 2016
Continuation 14676559 · Apr 1, 2015
Continuation 14517539 · Oct 17, 2014
Continuation 14047882 · Oct 7, 2013
Continuation 13699434
Related Publication 20190169590A1 · Jun 6, 2019