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 Jin; Kim Min Jae; Kang Yun Ji; Yoo Ji Yeon; 김정환
- 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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