The actinobacterial group is regarded as a reservoir of biologically
active natural products and hydrolytic enzymes with
the potential for biomedical and industrial applications. Here,
we present the complete genome sequence of Isoptericola
dokdonensis DS-3 isolated from soil in Dokdo, small islets
in the East Sea of Korea. This actinomycete harbors a large
number of genes encoding carbohydrate-degrading enzymes,
and its activity to degrade carboxymethyl cellulose into glucose
was experimentally evaluated. Since the genus Isoptericola was
proposed after reclassification based on phylogenetic analysis,
strains of Isoptericola have been continuously isolated from
diverse environments and the importance of this genus in the
ecosystem has been suggested by recent culturomic or metagenomic
studies. The phylogenic relationships of the genus
tended to be closer among strains that had been isolated from
similar habitats. By analyzing the properties of published genome
sequences of seven defined species in the genus, a large
number of genes for carbohydrate hydrolysis and utilization,
as well as several biosynthetic gene clusters for secondary
metabolites, were identified. Genomic information of I. dokdonensis
DS-3 together with comparative analysis of the genomes
of Isoptericola provides insights into understanding
this actinobacterial group with a potential for industrial applications.
In this study, the growth kinetics of Lactobacillus rhamnosus and lactic acid production in continuous culture were assessed at a range of dilution rates (0.05 h?1 to 0.40 h?1) using a 2 L stirred tank fermenter with a working volume of 600 ml. Unstructured models, predicated on the Monod and Luedeking-Piret equations, were employed to simulate the growth of the bacterium, glucose consumption, and lactic acid production at different dilution rates in continuous cultures. The maximum specific growth rate of L. rhamnosus, ┢max, was estimated at 0.40 h?1, and the Monod cell growth saturation constant, Ks, at approximately 0.25 g/L. Maximum cell viability (1.3 ≠ 1010 CFU/ml) was achieved in the dilution rate range of D = 0.28 h?1 to 0.35 h?1. Both maximum viable cell yield and productivity were achieved at D = 0.35 h?1. The continuous cultivation of L. rhamnosus at D = 0.35 h?1 resulted in substantial improvements in cell productivity, of 267% (viable cell count) that achieved via batch cultivation.