IP Library Granted Patent US 11,236,314
Granted Patent B2
US 11,236,314 · App. 15/940,578 · Granted Feb 1, 2022

Chimeric lysm polypeptides

Inventors: Chemira B. Appaiah (Bengaluru, IN); Vivek Daniel Paul (Bengaluru, IN); Rajagopalan Sanjeev Saravanan (Bengaluru, IN)
Assignee: Bactoclear Holdings PTE. Ltd
C12N9/2462C07K19/00C12N15/74C12Y302/01017
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Quick Facts
Patent No.
US 11,236,314
App. No.
15/940,578
Granted
Feb 1, 2022
Kind
B2
Abstract

Provided herein are antibacterial compositions and methods of making and using the compositions.

Claims (24)

1. A chimeric polypeptide, said chimeric polypeptide decreases the rate of growth of a Gram-negative bacterium, comprising:

(i) a LysM polypeptide segment exhibiting at least about 70% identity to SEQ ID NO: 2 and permitting the chimeric polypeptide access to the periplasmic space of the Gram-negative bacterium; and

(ii) a second polypeptide acting in the periplasmic space to decrease the rate of growth of the Gram-negative bacterium.

2. The chimeric polypeptide of claim 1 , wherein said decreased rate of growth results in decrease in population of said Gram-negative bacterium.

3. The chimeric polypeptide of claim 1 , wherein said second polypeptide comprises a sequence derived from a polypeptide from an organism different from the origin of said LysM polypeptide.

4. The chimeric polypeptide of claim 1 , wherein said Gram-negative bacterium is from a genus selected from Klebsiella, Acinetobacter, Pseudomonas , or Escherichia.

5. The chimeric polypeptide of claim 1 , wherein said LysM polypeptide segment exhibits at least about 80% or 90% identity to SEQ ID NO: 2.

6. The chimeric polypeptide of claim 1 , wherein said second polypeptide is derived from: (a) a phage endolysin; (b) a phage structure associated muralytic enzyme (ectolysin); (c) a lipopolysachharide binding protein (LBP); (d) an AntiMicrobial Peptide (AMP); or (e) a bactericidal permeability increasing protein (BPI).

7. The chimeric polypeptide of claim 1 , wherein said second polypeptide comprises 6×His or a segment from Gene Product 36-Catalytic Domain (GP36CD), phi29 endolysin, Bactericidal Permeability Increasing Protein-Transmembrane Domain (BPI TMD), Lipopolysaccharide Binding Protein (LBP), WLBU2, phiKZ, Gene Product 144 (GP144), Gene Product 181 (GP181) lysozyme, phi6 P5, BP7 lysozyme, or SUSHI peptide.

8. A composition comprising the chimeric polypeptide of claim 1 and a pharmaceutically acceptable excipient, carrier, or buffer or another antimicrobial agent.

9. A method of reducing the growth rate of a Gram-negative bacterium, said method comprising contacting said Gram-negative bacterium with said chimeric polypeptide of claim 1 .

10. A method of reducing the population of a Gram-negative bacterium, said method comprising contacting said Gram-negative bacterium with said chimeric polypeptide of claim 1 .

11. A chimeric polypeptide, said chimeric polypeptide accesses the periplasmic space of a Gram-negative bacterium from outside of the cell, comprising:

(i) a LysM polypeptide segment exhibiting at least about 70% identity to SEQ ID NO: 2 and permitting the chimeric polypeptide access to the periplasmic space of the Gram-negative bacterium; and

(ii) a second polypeptide acting in the periplasmic space to decrease the rate of growth of the Gram-negative bacterium.

12. The chimeric polypeptide of claim 11 , wherein at least some portion of said chimeric polypeptide accesses the periplasmic space of said Gram-negative bacterium; said access of said chimeric polypeptide results in a decrease in rate of growth of said Gram-negative bacterium.

13. The chimeric polypeptide of claim 11 , wherein said second polypeptide comprises a sequence derived from a polypeptide from an organism different from the origin of said LysM polypeptide.

14. The chimeric polypeptide of claim 11 , wherein said Gram-negative bacterium is from a genus selected from Klebsiella, Acinetobacter, Pseudomonas , or Escherichia.

15. The chimeric polypeptide of claim 11 , wherein said LysM polypeptide segment exhibits at least about 80% or 90% identity to SEQ ID NO: 2.

16. The chimeric polypeptide of claim 11 , wherein said second polypeptide is derived from: (a) a phage endolysin; (b) a phage structure associated muralytic enzyme (ectolysin); (c) a lipopolysachharide binding protein (LBP); (d) an AntiMicrobial Peptide (AMP); or (e) a bactericidal permeability increasing protein (BPI).

17. The chimeric polypeptide of claim 11 , wherein said second polypeptide comprises 6×His or a segment from Gene Product 36-Catalytic Domain (GP36CD), phi29 endolysin, Bactericidal Permeability Increasing Protein-Transmembrane Domain (BPI TMD), Lipopolysaccharide Binding Protein (LBP), WLBU2, phiKZ, Gene Product 144 (GP144), Gene Product 181 (GP181) lysozyme, phi6 P5, BP7 lysozyme, or SUSHI peptide.

18. A composition of the chimeric polypeptide of claim 11 and a pharmaceutically acceptable excipient, carrier, or buffer or another antimicrobial agent.

19. A method of reducing the growth rate of a Gram-negative bacterium, said method comprising contacting said Gram-negative bacterium with said chimeric polypeptide of claim 11 .

20. A method of reducing the population of a Gram-negative bacterium, said method comprising contacting said Gram-negative bacterium with said chimeric polypeptide of claim 11 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2020
From: GANGAGEN, INC.
To: BACTOCLEAR HOLDINGS PTE. LTD.
Reel/Frame 052603/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 30, 2018
From: APPAIAH, CHEMIRA B; PAUL, VIVEK DANIEL; SARAVANAN, RAJAGOPALAN SANJEEV
To: GANGAGEN, INC.
Reel/Frame 046498/0407 →
Continuity (2)
Provisional Application 62479028 · Mar 30, 2017
Related Publication 20200017843A1 · Jan 16, 2020