Chemoenzymatic methods for the synthesis of statins and statin intermediates

1. An isolated, synthetic or recombinant polypeptide having an aldolase activity comprising:

(i) an amino acid sequence having at least 95%, 96%, 97%, 98%, 99% sequence identity to SEQ ID NO:14;

(ii) an amino acid sequence encoded by a nucleic acid having at least 95%, 96%, 97%, 98%, 99% sequence identity to SEQ ID NO:13;

(iii) the amino acid sequence of (i) or (ii) lacking a signal sequence;

(iv) the amino sequence of (i), (ii) or (iii), further comprising a heterologous peptide or polypeptide;

(v) the amino acid sequence of (iv), wherein the heterologous peptide or polypeptide comprises a heterologous signal peptide or a heterologous prepro domain; or

(vi) the amino sequence of (iv) or (v), wherein the heterologous polypeptide or peptide is amino terminal to, carboxy terminal to or on both ends of a signal peptide, prepro domain or catalytic domain.

2. A composition comprising the polypeptide of claim 1 .

3. A heterodimer or a homodimer comprising the polypeptide of claim 1 and a second domain.

4. A chimeric polypeptide comprising at least a first domain comprising the polypeptide of claim 1 , and at least a second domain comprising a heterologous polypeptide or peptide.

5. A method for preparation of a compound having a formula as set forth as intermediate II in FIG. 7 , comprising the following steps:

(a) providing an aldol donor substrate;

(b) providing an aldol acceptor substrate;

(c) providing an aldolase of claim 1 ;

(d) admixing the aldol donor substrate of step (a), the aldol acceptor substrate of step (b), and the aldolase of step (c) under conditions wherein the aldolase can catalyze the aldol condensation reaction between the substrates of steps (a) and (b) thereby producing a compound comprising a structure as set forth as intermediate II in FIG. 7 .

6. The polypeptide of claim 1 , wherein the polypeptide has an aldolase activity, and wherein the aldolase activity comprises catalysis of the formation of a carbon-carbon bond; an aldol condensation; a 2-deoxyribose-5-phosphate aldolase (DERA) activity; catalysis of the condensation of acetaldehyde as donor and a 2(R)-hydroxy-3-(hydroxy or mercapto)-propionaldehyde derivative to form a 2-deoxysugar; catalysis of the condensation of acetaldehyde as donor and a 2-substituted acetaldehyde acceptor to form a 2,4,6-trideoxyhexose via a 4-substituted-3-hydroxybutanal intermediate; catalysis of the generation of chiral aldehydes using two acetaldehydes as substrates; enantioselective assembling of chiral β,δ-dihydroxyheptanoic acid side chains; enantioselective assembling of the core of [R—(R*,R*)]-2-(4-fluorophenyl)-b,d-dihydroxy-5-(1-methylethyl)-3-phenyl-4-(phenylamino)-carbonyl]-1H-pyrrole-1-heptanoic acid (atorvastatin); rosuvastatin or fluvastatin; with an oxidation step synthesis of a 3R,5S-6-chloro-2,4,6-trideoxy-erythro-hexonolactone; a thermotolerant aldolase activity; or a thermostable aldolase activity.

7. The polypeptide of claim 1 , wherein the polypeptide has the amino acid sequence of SEQ ID NO: 14.