Mutant lactobacillus beta-glucuronidase enzymes with enhanced enzymatic activity
Mutated Lactobacillus brevis strain 269Y β-glucuronidase enzymes with enhanced enzymatic activity at low pH (e.g., below pH 6.8), as well as enhanced thermostability as compared to wild type enzyme are provided. The enzymes of the invention advantageously allow for accurate analysis of bodily samples for the presence of drugs at low pH and in 30 minutes or less, as compared to the several hours needed using prior enzyme preparations. Methods of using the mutated enzymes for hydrolysis of glucuronide substrates, including opiates and benzodiazepines, are also provided.
1. A mutated Lactobacillus brevis strain 269Y β-glucuronidase (LbGUS) enzyme consisting of the amino acid sequence shown in SEQ ID NO: 2, wherein G564 in SEQ ID NO: 2 is substituted with an amino acid comprising a side chain comprising a non-aromatic hydroxyl group or histidine or asparagine.
2. The mutated LbGUS enzyme of claim 1 , wherein G564 in SEQ ID NO: 2 is substituted with serine.
3. The mutated LbGUS enzyme of claim 1 , wherein G564 in SEQ ID NO: 2 is substituted with threonine.
4. The mutated LbGUS enzyme of claim 1 , which has the amino acid sequence shown in SEQ ID NO: 7.
5. The mutated LbGUS enzyme of claim 4 , which is encoded by the nucleotide sequence shown in SEQ ID NO: 6.
6. A mutated Lactobacillus brevis strain 269Y β-glucuronidase (LbGUS) enzyme consisting of the amino acid sequence shown in SEQ ID NO: 2, wherein:
(i) G564 in SEQ ID NO: 2 is substituted with an amino acid comprising a side chain comprising a non-aromatic hydroxyl group or histidine or asparagine; and
(ii) a cysteine residue is appended at or near the carboxy terminus of the enzyme, wherein the carboxy terminus has the sequence: Xaa 0.8 -Cys-Xaa 0.2 , wherein Xaa=any amino acid (SEQ ID NO: 16).
7. The mutated LbGUS enzyme of claim 6 , wherein G564 in SEQ ID NO: 2 is substituted with serine.
8. The mutated LbGUS enzyme of claim 6 , wherein G564 in SEQ ID NO: 2 is substituted with threonine.
9. The mutated LbGUS enzyme of claim 6 , which has the amino acid sequence shown in SEQ ID NO: 11.
10. The mutated LbGUS enzyme of claim 9 , which is encoded by the nucleotide sequence shown in SEQ ID NO: 10.
11. A packaged formulation comprising a container comprising a preparation of the mutated LbGUS enzyme of claim 1 , which has an enzymatic activity of at least 5,000 Units/ml or 5,000 Units/mg.
12. The packaged formulation of claim 11 , which is an aqueous solution with an enzymatic activity of at least 50,000 Units/ml.
13. The packaged formulation of claim 11 , which is a lyophilized preparation with an enzymatic activity of at least 50,000 Units/mg.
14. The packaged formulation of claim 11 , wherein the preparation is stable at least six months at 2-8° C.
15. The packaged formulation of claim 11 , wherein the preparation lacks detectable sulfatase activity.
16. The mutated LbGUS enzyme of claim 1 , wherein G564 in SEQ ID NO: 2 is substituted with histidine.
17. The mutated LbGUS enzyme of claim 1 , wherein G564 in SEQ ID NO: 2 is substituted with asparagine.
18. The mutated LbGUS enzyme of claim 6 , wherein G564 in SEQ ID NO: 2 is substituted with histidine.
19. The mutated LbGUS enzyme of claim 6 , wherein G564 in SEQ ID NO: 2 is substituted with asparagine.
20. A packaged formulation comprising a container comprising a preparation of the mutated LbGUS enzyme of claim 6 , which has an enzymatic activity of at least 5,000 Units/ml or 5,000 Units/mg.
21. The packaged formulation of claim 20 , which is an aqueous solution with an enzymatic activity of at least 50,000 Units/ml.
22. The packaged formulation of claim 20 , which is a lyophilized preparation with an enzymatic activity of at least 50,000 Units/mg.
23. The packaged formulation of claim 20 , wherein the preparation is stable at least six months at 2-8° C.
24. The packaged formulation of claim 20 , wherein the preparation lacks detectable sulfatase activity.