Culture Conditions of E. coli Harboring Human O-Linked N-Acetyl-${\beta}$-Glucosaminidase Gene and Enzymatic Properties

사람의 O-linked-N-acetyl-${\beta}$-D-glucosaminidase 유전자를 함유한 대장균의 배양조건과 효소학적 특성

  • 강대욱 (창원대학교 보건ㆍ생화학과) ;
  • 조용권 (창원대학교 보건ㆍ생화학) ;
  • 서현효 (진주 산업대학교 환경공학과)
  • Published : 2004.06.01

Abstract

Protein modification by N-acetyl-${\beta}$-D-glucosamine (O-G1cNAc) on the hydroxyl groups of Ser or Thr ubiq-uitously occurs in eukaryotic cells and is involved in many cellular phenomena. The level of O-G1cNAc-mod-ified protein is regulated by OGT and O-GlcNAcase enzymes. We have tried to produce recombinant O-GlcNAcase in E. coli as an effort to establish in vitro screening system for modulators of O-GlcNAcase. The culture conditions for improvement of O-GlcNAcase productivity, were as follows: induction temperature, $30^{\circ}C$; the concentration of L-arabinose, 0.02% and induction time, 5 hr. Under these culture conditions, E. coli cells containing O-GlcNAcase gene had no enzyme activity until up to 3 hr culture. However, O-GlcNAcase activity dramatically increased from 3 to 5 hr culture. It almost maintained the same level after 5 hr culture. Western blot analysis verified the amount of expressed O-GlcNAcase increased with culture time, being con-sistent with activity data. The optimal reaction condition determined in this study was as follows: protein quan-tity, $5{\mu}g$; reaction time, 30 min; reaction temperature, $45^{\circ}C$; substrate concentration, 2 mM; reaction pH, 6.5. Methanol had little effect on O-GlcNAcase activity and 90% of activity were retained at 10%. Only 15% resid-ual activity were detected at 5% of chloroform.

단백질의 serine이나 threonine의 수산기에 N-acetyl-${\beta}$-D-glucosamine (O-GlcNAc)으로 변형되는 당쇄는 대부분의 진핵세포에서 광범위하게 일어나는 번역 후 수식의 일종으로 여러 세포 내 현상에 관여하고 있다. O-GlcNAc의 변형정도는 O-GlcNAc transfearse (OGT)와 O-linked N-acetyl-${\beta}$-D-glucosaminidase (O-GlcNAcase)에 의해 조절된다. O-GlcNAcase의 효소활성 조절물질을 탐색하기 위한 시험관 내 검정계를 확립하기 위해 재조합 O-GlcNAcase의 생산을 시도하였다. O-GlcNAcase 발현을 최적화하기 위한 배양조건을 검토한 결과 유도 배양온도 $30^{\circ}C$, 유도제인 L-arabinose 0.02%, 유도 배양시간 5시간 등으로 나타났다. 위의 조건에서 대장균 형질전환체를 배양하면서 한 시간 간격으로 배양액을 채취하여 세포를 파괴하고 얻은 효소용액의 활성은 배양 후 3시간에서 5시간까지는 급격히 증가하였으나 그 이후는 거의 증가하지 않았다. Western blot으로 발현된 단백질 양을 조사한 결과는 활성 그래프와 비슷한 양상을 보였다. 이렇게 생산한 O-GlcNAcase의 최적 반응조건은 pH 6.5, 반응온도 $45^{\circ}C$, 기질의 농도 2 mM, pH 6.5로 나타났다.

Keywords

References

  1. Diabetes v.48 Localization of the O-GlcNAc transferase in rat pancreas Akimoto,Y.;L.K.Kreppel;H.Hirano;G.W.Hart https://doi.org/10.2337/diabetes.48.12.2407
  2. Diabetologia v.43 Increased O-GlcNAc transferase in pancreas of rats with streptozotocon-induced diabetes Akimoto,Y.;L.K.Kreppel;H.Hirano;G.W.Hart https://doi.org/10.1007/s001250051519
  3. J. Biol. Chem. v.276 Dynamic O-glycosylation of nuclear and cytosolic proteins: cloning and characterization of a neutral, cytosolic beta-N-acetylglu-cosaminidase from human brain Gao,Y.;L.Wells;F.I.Comer;G.J.Parker;G.W.Hart https://doi.org/10.1074/jbc.M010420200
  4. Biochem. Biophys. Res. Commun. v.213 O-Linked N-acetylglucosamine is upregulated in Alzheimer brains Griffith,L.S.;B.Schmitz https://doi.org/10.1006/bbrc.1995.2149
  5. Eur. J. Biochem. v.262 O-Linked N-acetylglu-cosamine levels in cerebellar neurons respond reciprocally to perturbations of phosphorylation Griffith,L.S.;B.Schmitz https://doi.org/10.1046/j.1432-1327.1999.00439.x
  6. J. Neurosci. Res. v.41 β-Amyloid precursor protein is modified with O-linked N-acetylglucosamine Griffith,L.S.;M.Mathes;B.Schmitz https://doi.org/10.1002/jnr.490410214
  7. Arch. Biochem. Biophys. v.362 Elevated O-linked N-acetylglucosamine metabolism in pancreatic β-cells Hanover,J.A.;Z.Lai;G.Lee;W.A.Lubas;S.M.Sato https://doi.org/10.1006/abbi.1998.1016
  8. FASEB J. v.15 Glycan-dependent signaling: O-linked N-acetylglucosamine Hanover,J.A. https://doi.org/10.1096/fj.01-0094rev
  9. J. Mol. Med. v.10 The role of O-linked protein glycosylation in β-cell dysfunction Kondra,R.J.;J.E.Kudlow
  10. Mol. Genet. Metabol. v.77 The O-GlcNAcase theory of diabetes: commentary on a candidate gene for diabetes Kudlow,J.E. https://doi.org/10.1016/S1096-7192(02)00128-2
  11. Nature v.227 Cleavage of structural proteins during the assembly of the head of bacteriophage T4 Laemmli,U.K. https://doi.org/10.1038/227680a0
  12. Trends Neurosci. v.24 Susceptibility gene(s) for Alzheimer;s disease on chromosome 10 Lendon,C.;N.Craddock https://doi.org/10.1016/S0166-2236(00)01912-3
  13. Proc. Natl. Acad. Sci. v.97 Glucose stimulates protein modification by O-linked GlcNAc in pancreatic β-cell;linkage of O-linked GlcNAc to β-cell death Liu,K.;K.L.Andrew;E.Chin;J.E.Kudlow https://doi.org/10.1073/pnas.97.6.2820
  14. J. Biol. Chem. v.272 O-Linked GlcNAc transferase is a conserved nucleocytoplasmic protein containing tetratricopeptide repeats Lubas,W.A.;D.W.Frank;M.Krause;J.A.Hanover https://doi.org/10.1074/jbc.272.14.9316
  15. Diabetes v.45 Hexosamine and insulin resistance McClain,D.A.;E.D.Crook https://doi.org/10.2337/diabetes.45.8.1003
  16. Proc. Natl. Acad. Sci. v.99 Altered glycan-dependent signaling induces insulin resistance and hyperleptinemia McClain,D.A.;W.A.Lubas;R.C.Cooksey;M.Hazel;G.J.Parker;D.C.Love;J.A.Hanover https://doi.org/10.1073/pnas.152346899
  17. J. Biol. Chem. v.259 Topography and polypeptide distribution of terminal N-acetylglucosamine residues on the surfaces of intact lymphocytes: evidence for O-linked GlcNAc Torres,C.R.;G.W.Hart
  18. J. Biol. Chem. v.277 Dynamic O-glycosylation of nuclear and cytosolic proteins:further characterization of the nucleocytoplasmic β-N-acetylglucosaminidase Wells,L.;Y.Gao;J.A.Mahoney;K.Vosseller;C.Chen;A.Rosen;G.W.Hart https://doi.org/10.1074/jbc.M109656200
  19. Biochem. Biophys. Res. Commun. v.302 O-GlcNAc: a regulatory post-translational modification Wells,L.;S.A.Whelan;G.W.Hart https://doi.org/10.1016/S0006-291X(03)00175-X
  20. Trends Cell Biol. v.14 O-GlcNAc modification: a nutritional sensor that modulates proteasome function Zachara,N.E.;G.W.Hart https://doi.org/10.1016/j.tcb.2004.03.005