The invention relates to nitrilases and to nucleic acids encoding the nitrilases. In addition methods of designing new nitrilases and method of use thereof are also provided. The nitrilases have increased activity and stability at increased pH and temperature.
1. An isolated, synthetic, or recombinant polynucleotide that encodes a polypeptide having nitrilase activity selected from a group consisting of:
(a) a variant of SEQ ID NO:189 having the nucleic acid sequence 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99%, identical to SEQ ID NO: 189, and the variant nucleic acid sequence encodes a polypeptide having a nitrilase activity; or
(b) a nucleic acid sequence completely complementary to (a).
2. An expression cassette, a vector, or a cloning vehicle comprising the nucleic acid sequence as forth in claim 1 .
3. A transformed non-human cell comprising:
(i) the expression cassette, the vector, or the cloning vehicle as set forth in claim 2 ;
(ii) the transformed cell of (i), where the cell is
(a) a gram negative bacteria, a gram positive bacteria, or a eukaryotic organism;
(b) an Escherichia coli;
(c) a Streptomyces diversa, Lactobacillus gasseri, Lactococcus lactis, Lactococcus cremoris , or a Bacillus subtilis ; or
(d) a Saccharomyces cerevisiae, Schizosaccharomyces pombe, Pichia pastoris, Kluyveromyces lactis, Hansenula polymorpha , or an Aspergillus niger.
4. A transgenic non-human organism comprising the nucleic acid of claim 1 .
5. An isolated, synthetic, or recombinant polynucleotide that encodes a polypeptide having nitrilase activity, wherein the polynucleotide is the nucleic acid sequence of SEQ ID NO: 189, wherein the nucleic acid is operably joined to a heterologous promoter.
6. A recombinant expression cassette, a vector, or a cloning vehicle comprising the nucleic acid sequence of SEQ ID NO:189, operably joined to a heterologous promoter as forth in claim 5 .