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US 2017/0247732 A1Published application
Methods of Producing Testosteronan Polymers Using Testosteronan Synthase
AssigneeThe Board of Regents of the University of Oklahoma
InventorsPaul L. DeAngelis, Nigel J. Otto
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Abstract
Testosteronan, a heparosan analog having the structure [-4-D-GlcUA-α1,4-D-GlcNAc-α1-]n, is produced by testosteronan synthase, a single protein that is a dual-action catalyst that utilizes UDP-GlcUA and UDP-GlcNAc to synthesize a polysaccharide having the structure [-4-D-GlcUA-α1,4-D-GlcNAc-α1-]n.
Claims20
A method of producing a polymer, at least a portion of which has the repeat structure [4-D-glucuronic acid-α1,4-D-N-acetylglucosamine-α1-]n ([-4-D-GlcUA-α1,4-D-GlcNAc-α1-]n, the method comprising the steps of:
- culturing a host cell made recombinant by addition of a nucleotide sequence encoding an enzymatically active testosteronan synthase, wherein the testosteronan synthase is a single protein that is a dual-action catalyst that utilizes UDP-GlcUA and UDP-GlcNAc to synthesize a polymer having the repeat structure [-4-D-GlcUA-α1,4-D-GlcNAc-α1-]n, wherein the recombinant host cell is cultured under conditions that allow for the production of a polymer having the repeat structure [-4-D-GlcUA-α1,4-D-GlcNAc-α1-]n;
- and
- isolating the polymer having the repeat structure [-4-D-GlcUA-α1,4-D-GlcNAc-α1-]n.
A recombinant vector, comprising:
- a nucleotide sequence encoding an enzymatically active testosteronan synthase, wherein the testosteronan synthase is a single protein that is a dual-action catalyst that utilizes UDP-GlcUA and UDP-GlcNAc to synthesize a polymer having the repeat structure [-4-D-GlcUA-α1,4-D-GlcNAc-α1-]n, and wherein the nucleotide sequence encoding the enzymatically active testosteronan synthase comprises at least one of:
- (a) the nucleotide sequence of SEQ ID NO:2;
- (b) a nucleotide sequence encoding the amino acid sequence of SEQ ID NO:1;
- (c) a nucleotide sequence that is at least 90% identical to SEQ ID NO:2;
- (d) a nucleotide sequence encoding an amino acid sequence that is at least 90% identical to SEQ ID NO:1;
- (e) a nucleotide sequence capable of hybridizing to a complement of SEQ ID NO:2 under hybridization conditions of at least one of:
- (1) hybridization at a temperature of 68° C. in 5×SSC/5× Denhardt's solution/1.0% SDS, followed with washing in 3×SSC at 42° C.;
- and
- (2) hybridization at a temperature of 30° C. in 5×SSC, 5× Denhardt's reagent, 30% formamide for about 20 hours followed by washing twice in 2×SSC,0.1% SDS at about 30° C. for about 15 minutes followed by 0.5×SSC, 0.1% SDS at about 30° C. for about 30 minutes;
- (f) a nucleotide sequence capable of hybridizing to a complement of a nucleotide sequence encoding the amino acid sequence of SEQ ID NO:1 under hybridization conditions of at least one of (1) and (2) of (e) above;
- and
- (g) a nucleotide sequence encoding an amino acid sequence having up to 50 amino acid insertions, deletions or substitutions when compared to SEQ ID NO:1;
- (h) a nucleotide sequence encoding an amino acid sequence having up to 25 amino acid insertions, deletions or substitutions when compared to SEQ ID NO:1.
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Dependencies are inferred from the claim text.