J. Mergaert et al., ISOLATION AND IDENTIFICATION OF POLY(3-HYDROXYVALERATE)-DEGRADING STRAINS OF PSEUDOMONAS-LEMOIGNEI, International journal of systematic bacteriology, 46(3), 1996, pp. 769-773
By using selective enrichment of polyhydroxyalkanoate-degrading bacter
ia and poly(3-hydroxyvalerate)-containing granules from Chromobacteriu
m violaceum as the carbon source, 10 new Pseudomonas lemoignei strains
were isolated; these strains were able to degrade poly(3-hydroxyvaler
ate), as well as poly(3-hydroxybutyrate), in vitro. The new isolates w
ere characterized and identified by comparing them with P. lemoignei L
MG 2207(T) (T = type strain). Like P. lemoignei LMG 2207(T) cells, the
cells of the 10 new isolates contained mainly hexadecenoic, hexadecan
oic, octadecenoic, and dodecanoic acids, as well as hydroxylated fatty
acids, and exhibited respiration in the presence of methylpyruvate, 3
-hydroxybutyrate, and 4-hydroxybutyrate, but not in the presence of th
e 92 other carbon sources included in Biolog GN microplates. The prote
in patterns of the new isolates were almost identical to each other an
d very similar to the protein pattern of P. lemoignei LMG 2207(T). Som
e of the new isolates, but not P. lemoignei LMG 2207(T), contained meg
aplasmids that were about 200 kbp long. The 16S ribosomal DNA genes of
strain A62, a representative of the 10 new isolates, and of P. lemoig
nei LMG 2207(T) exhibited more than 0.99 sequence similarity. The DNA-
DNA reassociation value for two representative strains was 100%, and t
he levels of DNA-DNA reassociation between these strains and the type
strain were 60 and 61%. The taxonomy of P. lemoignei is briefly discus
sed.