Identification of proteolytic bacteria from the Arctic Chukchi Sea expedition cruise and characterization of cold-active proteases
Cited 6 time in
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Title
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Identification of proteolytic bacteria from the Arctic Chukchi Sea expedition cruise and characterization of cold-active proteases
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Authors
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Park, Ha Ju
Lee, Yung Mi
Kim, Sunghui
Wi, Ah Ram
Han, Se Jong
Kim, Han-Woo
Kim, Il-Chan
Yim, Joung Han
Kim, Dockyu
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Subject
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Microbiology
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Keywords
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Arctic; Cold-active enzyme; Expedition cruise; Protease; Pseudoalteromonas; Araon
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Issue Date
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2014
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Citation
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Park, Ha Ju, et al. 2014. "Identification of proteolytic bacteria from the Arctic Chukchi Sea expedition cruise and characterization of cold-active proteases". Journal of Microbiolog, 52(10): 825-833.
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Abstract
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Chukchi Sea expedition cruise of the Korean icebreaker
Araon in 2012, a total of 15,696 bacteria were randomly isolated
from Marine Broth 2216 agar plates. Of these, 2,526
(16%) showed proteolytic activity and were identified as
mainly Alteromonas (31%), Staphylococcus (27%), and Pseudoalteromonas
(14%). Among the proteolytic strains, seven
were selected based on their significant ability to grow and
produce a halo on skim milk plates at low temperatures
(<5°C) owing to cold-active proteases. These strains were
affiliated with the genus Pseudoalteromonas and were divided
into three groups based on phylogenetic analysis of the 16S
rRNA genes. Profiling cell membrane fatty acids confirmed
the 16S rRNA-based differentiation and revealed the accordance
between the two analyses. Seven genes for serine protease
precursors were amplified from the corresponding
strains, and based on sequence similarities, these genes were
divided into three groups that were identical to those identified
by the 16S rRNA phylogenetic analysis. Three protease
genes from the representative strains of each group
were composed of 2,127-2,130 bp, encoding 708-709 amino
acids, and these genes yielded products with calculated molecular
weights of approximately 72.3-72.8 kDa. Amino acid
sequence analysis suggested that the precursors are members
of the subtilase serine endo- and exo-peptidase clan and contain
four domains (signal peptide, N-terminal prosequence,
catalytic domain, and two pre-peptidase C-terminal domains).
Upon expression in E. coli, each recombinant protease exhibited
proteolytic activity on zymogram gels.
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DOI
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http://dx.doi.org/10.1007/s12275-014-4226-6
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Type
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Article
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Station
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Araon
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- 2011-2016, Exploration of Future Resources in The Polar Oceans and Study on Their Utilization (K-POD) (11-16) / Yim; Joung Han (PM11090; PM12030; PM13030; PM14050; PM15050)
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