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Cloning and Characterization of a Methionine Aminopeptidase (MAP) Gene from Tetragenococcus halophilus CY54 Isolated from Myeolchi-JeotgalCloning and Characterization of a Methionine Aminopeptidase (MAP) Gene from Tetragenococcus halophilus CY54 Isolated from Myeolchi-Jeotgal

Other Titles
Cloning and Characterization of a Methionine Aminopeptidase (MAP) Gene from Tetragenococcus halophilus CY54 Isolated from Myeolchi-Jeotgal
Authors
Kim Tae JinKim Min JaeKang Yun JiYoo Ji Yeon김정환
Issue Date
Mar-2023
Publisher
한국미생물·생명공학회
Keywords
Tetragenococcus halophilus; methionine aminopeptidase; map gene; proteolytic system
Citation
한국미생물·생명공학회지, v.51, no.1, pp 26 - 31
Pages
6
Indexed
SCOPUS
Journal Title
한국미생물·생명공학회지
Volume
51
Number
1
Start Page
26
End Page
31
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/59237
DOI
10.48022/mbl.2301.01005
ISSN
1598-642X
Abstract
A map gene encoding methionyl-specific aminopeptidase (MAP; EC 3.4.11.18) was cloned from Tetragenococcus halophilus CY54. Translated amino acid sequence of CY54 MAP showed high similarities with those from Enterococcus faecalis (83.8%) and Streptococcus salivarius (62.2%) but low similarities with MAPs from Lactobacillus and Lactococcus genera. The map gene was overexpressed in E. coli BL21(DE3) using pET26b(+), and the recombinant MAP was purified by using an Ni-NTA column. The size of recombinant MAP was 29 kDa as determined by SDS-PAGE. The optimum pH and temperature of CY54 MAP were pH 5.0 and 60℃, respectively. The activity of CY54 MAP was most significantly increased by Co2+ ion (159%), and showed the highest activity at 12% NaCl. Km and Vmax were 0.64 ± 0.006 mM and 10.12 ± 0.014 U/mg protein, respectively when met-pNA was used as the substrate. This is the first report on a MAP from Tetragenococcus species.
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농업생명과학대학 (식품공학부)
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