Using a DNA probe from the gene encoding squalene-hopene cyclase (SHC,
EC 5.4.99.-) from the Gram-positive bacterium Alicyclobacillus acidoc
aldarius, we have cloned a 4.3 kb HindIII fragment of chromosomal DNA
from Zymomonas mobilis. An open reading frame of 1977 bp was detected
that could encode a protein of 658 amino acids with a calculated molec
ular mass of 74077 Da. Under the control of lac or tac promoters, this
gene, shc, was expressed in Escherichia coil K12 strains and its prod
uct had squalene-hopene cyclase activity. Sequence alignments with the
A. acidocaldarius SHC, the lanosterol cyclase of the yeast Candida al
bicans. and the cycloartenol synthase of the plant Arabidopsis thalian
a revealed six highly conserved regions (mainly in the C-terminal part
) of the proteins. These regions contained the core motif Gln-X-X-X-Gl
y-X-Trp.