IP Library Granted Patent US 9,301,996
Granted Patent B2
US 9,301,996 · App. 14/676,559 · Granted Apr 5, 2016

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.
A61K38/50A61K31/43A61K31/545A61K45/06C12N9/86A61K38/00C12Y305/02006
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Quick Facts
Patent No.
US 9,301,996
App. No.
14/676,559
Granted
Apr 5, 2016
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 (26)

1. A method for degrading an antibiotic in a patient's gastrointestinal (GI) tract, comprising administering an effective amount of a beta-lactamase to the patient, wherein:

the antibiotic is a beta-lactam antibiotic selected from a penicillin and a cephalosporin,

the beta-lactamase comprises an amino acid sequence having at least 90% sequence identity with SEQ ID NO: 1 and an asparagine (N) or arginine (R) at a position corresponding to position 276 according to Ambler classification, 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 method of claim 1 , wherein the cephalosporin is selected from cefoperazone and ceftriaxone.

3. The method of claim 2 , wherein the cephalosporin is ceftriaxone.

4. The method of claim 1 , wherein the penicillin is selected from amoxicillin, ampicillin, and piperacillin.

5. The method of claim 1 , wherein the antibiotic has been excreted into the patient's GI tract.

6. The method of claim 1 , wherein the antibiotic is administered to the patient intraveneously.

7. The method of claim 1 , wherein the beta-lactamase is administered to the patient orally.

8. The method of claim 1 , wherein the beta-lactamase is administered simultaneously to or sequentially with the beta-lactam antibiotic.

9. The method of claim 8 , wherein the beta-lactamase is administered before the beta-lactam antibiotic.

10. The method of claim 1 , wherein the beta-lactamase inactivates unabsorbed antibiotic in the patient's GI tract.

11. The method of claim 1 , wherein the beta-lactamase comprises an amino acid sequence of SEQ ID NO: 1 with an asparagine (N) or arginine (R) residue at position 276 according to Ambler classification.

12. A method for degrading an antibiotic in a patient's gastrointestinal (GI) tract, comprising administering an effective amount of a beta-lactamase to the patient, wherein:

the antibiotic is a beta-lactam antibiotic selected from a penicillin and a cephalosporin,

the beta-lactamase comprises an amino acid sequence having at least 95% identity with SEQ ID NO: 1 and an asparagine (N) or arginine (R) residue at position 276 according to Ambler classification, 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.

13. The method of claim 12 , wherein the cephalosporin is selected from cefoperazone and ceftriaxone.

14. The method of claim 12 , wherein the penicillin is selected from amoxicillin, ampicillin, and piperacillin.

15. The method of claim 12 , wherein the antibiotic has been excreted into the patient's GI tract.

16. The method of claim 12 , wherein the antibiotic is administered to the patient intraveneously.

17. The method of claim 12 , wherein the beta-lactamase is administered to the patient orally.

18. The method of claim 12 , wherein the beta-lactamase is administered simultaneously to or sequentially with the beta-lactam antibiotic.

19. The method of claim 12 , wherein the beta-lactamase inactivates unabsorbed antibiotic in the patient's GI tract.

20. The method of claim 12 , wherein the beta-lactamase comprises an amino acid sequence of SEQ ID NO: 1 with an asparagine (N) or arginine (R) residue at position 276 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 Apr 1, 2015
From: KOSKI, PERTTI; AIRAKSINEN, ULLA; VALIMAKI, KATJA
To: PREV ABR LLC
Reel/Frame 035315/0143 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2015
From: PREV ABR LLC
To: SYNTHETIC BIOLOGICS, INC.
Reel/Frame 035315/0161 →
Priority Claims (1)
FI 20105572 · May 24, 2010 · national
Continuity (4)
Continuation 14517539 · Oct 17, 2014
Continuation 14047882 · Oct 7, 2013
Continuation 13699434
Related Publication 20150209418A1 · Jul 30, 2015