ABSTRACT
Strain JW12T, isolated from surface seawater of the Arabian Sea, was subjected to characterization by a polyphasic taxonomic approach. Cells of the isolate were Gram-stain-negative, aerobic and rod-shaped. It accumulated poly-ß-hydroxybutyrate. On the basis of 16S rRNA gene sequence analysis, strain JW12T was closely related to Alteromonas confluentis, with 16S rRNA gene sequence similarity of 98.0â%. Phylogenetic analysis revealed that it fell within the cluster of the genus Alteromonas and represented one independent lineage with A. confluentis. The average nucleotide identity (ANI) value and the genome-to-genome distance between strain JW12T and A. confluentis KCTC 42603T were 70.0 and 21.3â%, respectively. The sole respiratory quinone was ubiquinone-8 (Q8). The principal fatty acids were summed feature 3 (C16â:â1ω7c and/or iso-C15â:â0 2-OH), C16â:â0 and C18â:â1ω7c. The major polar lipids included phosphatidylethanolamine, phosphatidylglycerol, two unidentified glycolipids and one aminophospholipid. The DNA G+C content was 48.4 mol%. Differential phylogenetic distinctiveness and chemotaxonomic differences, together with phenotypic properties obtained in this study, revealed that strain JW12T could be differentiated from the closely related species. Therefore, it is proposed that strain JW12T represents a novel species in the genus Alteromonas, for which the name Alteromonas lipolytica sp. nov. (type strain, JW12T=CGMCC 1.15735T=KCTC 52408T=MCCC 1K03175T), is proposed.
Subject(s)
Alteromonas/classification , Hydroxybutyrates/metabolism , Phylogeny , Polyesters/metabolism , Seawater/microbiology , Alteromonas/genetics , Alteromonas/isolation & purification , Bacterial Typing Techniques , Base Composition , DNA, Bacterial/genetics , Fatty Acids/chemistry , Indian Ocean , Nucleic Acid Hybridization , Phospholipids/chemistry , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNAABSTRACT
Altererythrobacter ishigakiensis NBRC 107699 was isolated from marine sediment collected from a site on the coast of Ishigaki Island, Japan and deposited to the NITE Biological Resource Center. This strain is able to produce astaxanthin, which can be used as a food supplement. Here we describe the genome sequence and annotation, as well as the features of the organism. The genome of strain NBRC 107699 comprises 2,673,978bp and contains 2618 protein-coding genes (1966 with predicted functions), 42 tRNA genes and 3 rRNA genes. A. ishigakiensis NBRC 107699T encodes fifteen genes related to astaxanthin production, revealing its potential application in biotechnological industry. The genome sequence of A. ishigakiensis NBRC 107699 now provides the fundamental information for future studies.
Subject(s)
Alphaproteobacteria/genetics , Genome, Bacterial , RNA, Bacterial/genetics , Alphaproteobacteria/metabolism , Japan , Molecular Sequence Annotation , Sequence Analysis, DNA , Xanthophylls/metabolismABSTRACT
The angiotensin-I-converting enzyme (ACE) inhibitory peptides from mussel, Mytilus coruscus, were investigated and the variable factors, protease concentration, hydrolysis time, pH, and temperature, were optimized using Uniform Design, a new statistical experimental method. The results proved that the hydrolysate of alkali proteases had high ACE-inhibitory activity, especially the alkali protease E1. Optimization by Uniform Design showed that the best hydrolysis conditions for preparation of ACE-inhibitory peptides from Mytilus coruscus were protease concentration of 36.0 U/mL, hydrolysis time of 2.7 hours, pH 8.2, and Temperature at 59.5°C, respectively. The verification experiments under optimum conditions showed that the ACE-inhibitory activity (91.3%) were agreed closely with the predicted activity of 90.7%. The amino acid composition analysis of Mytilus coruscus ACE-inhibitory peptides proved that it had high percent of lysine, leucine, glycine, aspartic acid, and glutamic acid.
