IP Library Granted Patent US 9,034,602
Granted Patent B2
US 9,034,602 · App. 13/699,434 · Granted May 19, 2015

Modified beta-lactamases and methods and uses related thereto

Inventors: Pertti Koski (Helsinki, FI); Ulla Airaksinen (Vantaa, FI); Katja Valimaki (Vantaa, FI)
Assignee: Synthetic Biologics, Inc.
A61K38/50A61K38/00C12N9/86A61K45/06A61K31/43A61K31/545C12Y305/02006
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Quick Facts
Patent No.
US 9,034,602
App. No.
13/699,434
Granted
May 19, 2015
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 (21)

1. A beta-lactamase, comprising an amino acid sequence having at least 90% sequence identity with SEQ ID NO: 1 and a hydrophilic amino acid residue other than aspartic acid (D) at a position corresponding to position 276 according to Ambler classification, wherein:

the hydrophilic amino acid residue is arginine (R) and

the beta-lactamase hydrolyzes ceftriaxone substantially more efficiently than a beta-lactamase of SEQ ID NO: 1 that has an aspartic acid (D) at a position corresponding to position 276 according to Ambler classification.

2. The beta-lactamase according to claim 1 , wherein the hydrophilic amino acid residue is located in an alpha helix.

3. The beta-lactamase according to 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 beta-lactamase according to claim 1 , wherein the beta-lactamase hydrolyzes a penicillin and a cephalosporin.

5. The beta-lactamase according to claim 4 , wherein the cephalosporin is selected from cefoperazone and ceftriaxone.

6. The beta-lactamase according to claim 1 , wherein the amino acid sequence has at least 93% sequence identity with SEQ ID NO: 1.

7. The beta-lactamase according to claim 1 , wherein the amino acid sequence has at least 95% sequence identity with SEQ ID NO: 1.

8. A beta-lactamase comprising an amino acid sequence of SEQ ID NO: 1 with an arginine (R) residue at position 276 according to Ambler classification.

9. The beta-lactamase according to claim 8 , wherein the beta-lactamase hydrolyzes a cephalosporin and a penicillin.

10. The beta-lactamase according to claim 9 , wherein the cephalosporin is selected from cefoperazone and ceftriaxone.

11. The beta-lactamase according to claim 8 , wherein the beta-lactamase is suitable for hydrolyzing a cephalosporin that has been excreted into the gastrointestinal tract.

12. A pharmaceutical composition comprising the beta-lactamase according to claim 1 .

13. A pharmaceutical composition for oral administration comprising an effective amount of a beta-lactamase comprising an amino acid sequence having at least 90% sequence identity with SEQ ID NO: 1 and a hydrophilic amino acid residue other than aspartic acid (D) at a position corresponding to position 276 according to Ambler classification, wherein:

the hydrophilic amino acid residue is arginine (R) and

the beta-lactamase hydrolyzes ceftriaxone substantially more efficiently than a beta-lactamase of SEQ ID NO: 1 that has an aspartic acid (D) at a position corresponding to position 276 according to Ambler classification.

14. The pharmaceutical composition according to claim 13 , wherein the beta-lactamase hydrolyzes a penicillin and a cephalosporin.

15. The pharmaceutical composition according to claim 14 , wherein the cephalosporin is selected from cefoperazone and ceftriaxone.

16. The pharmaceutical composition according to claim 13 , wherein the beta-lactamase comprises an amino acid sequence of at least 93% sequence identity with SEQ ID NO: 1.

17. The pharmaceutical composition according to claim 13 , wherein the beta-lactamase comprises an amino acid sequence of at least 95% sequence identity with SEQ ID NO: 1.

Assignments (4)
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 Jun 25, 2013
From: KOSKI, PERTTI; AIRAKSINEN, ULLA; VALIMAKI, KATJA
To: PREV ABR LLC
Reel/Frame 030676/0769 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2013
From: PREV ABR LLC
To: SYNTHETIC BIOLOGICS, INC.
Reel/Frame 030673/0244 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2012
From: KOSKI, PERTTI; AIRAKSINEN, ULLA; VALIMAKI, KATJA
To: PREV ABR LLC
Reel/Frame 029349/0260 →
Priority Claims (1)
FI 20105572 · May 24, 2010 · national
Continuity (1)
Related Publication 20130216622A1 · Aug 22, 2013