Engineered purine nucleoside phosphorylase variant enzymes
US-11162105-B2 · Nov 2, 2021 · US
US12110493B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12110493-B2 |
| Application number | US-202117490215-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 30, 2021 |
| Priority date | Jul 9, 2018 |
| Publication date | Oct 8, 2024 |
| Grant date | Oct 8, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention provides engineered purine nucleoside phosphorylase (PNP) enzymes, polypeptides having PNP activity, and polynucleotides encoding these enzymes, as well as vectors and host cells comprising these polynucleotides and polypeptides. Methods for producing PNP enzymes are also provided. The present invention further provides compositions comprising the PNP enzymes and methods of using the engineered PNP enzymes. The present invention finds particular use in the production of pharmaceutical compounds.
Opening claim text (preview).
We claim: 1. A polynucleotide sequence encoding an engineered purine nucleoside phosphorylase comprising a polypeptide sequence having at least 85% sequence identity to SEQ ID NO:2, wherein the polypeptide sequence of said engineered purine nucleoside phosphorylase comprises a substitution at position 65 and wherein the polypeptide sequence is numbered with reference to SEQ ID NO: 2, and wherein said engineered purine nucleoside phosphorylase comprises improved activity on compound 3 as compared to wild-type E. coli purine nucleoside phosphorylase. 2. The polynucleotide sequence of claim 1 , wherein said polynucleotide sequence is operably linked to a control sequence. 3. The polynucleotide sequence of claim 1 , wherein said polynucleotide sequence is codon optimized. 4. The polynucleotide sequence of claim 1 , wherein said polynucleotide sequence comprises the polynucleotide sequence as set forth in SEQ ID NO: 5. 5. An expression vector comprising the polynucleotide sequence of claim 1 . 6. A host cell comprising the expression vector of claim 5 . 7. A host cell comprising the polynucleotide sequence of claim 1 . 8. A method of producing an engineered purine nucleoside phosphorylase in a host cell, comprising culturing the host cell of claim 7 , under suitable conditions, such that the engineered purine nucleoside phosphorylase is produced. 9. The method of claim 8 , further comprising recovering the engineered purine nucleoside phosphorylase from the culture and/or host cell. 10. The method of claim 9 , further comprising a step of purifying said engineered purine nucleoside phosphorylase.
Purine-nucleoside phosphorylase (2.4.2.1) · CPC title
Pentosyltransferases (2.4.2) · CPC title
Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.