TY - JOUR
T1 - Enzyme replacement therapy for Morquio A
T2 - An active recombinant N-acetylgalactosamine-6-sulfate sulfatase produced in Escherichia coli BL21
AU - Rodríguez, Alexander
AU - Espejo, Ángela J.
AU - Hernández, Alejandra
AU - Velásquez, Olga L.
AU - Lizaraso, Lina M.
AU - Cordoba, Henry A.
AU - Sánchez, Oscar F.
AU - Alméciga-Díaz, Carlos J.
AU - Barrera, Luis A.
PY - 2010/11
Y1 - 2010/11
N2 - Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive disorder caused by N-acetylgalactosamine-6-sulfate sulfatase (GALNS) deficiency. Currently no effective therapies exist for MPS IVA. In this work, production of a recombinant GALNS enzyme (rGALNS) in Escherichia coli BL21 strain was studied. At shake scale, the effect of glucose concentration on microorganism growth, and microorganism culture and induction times on rGALNS production were evaluated. At bench scale, the effect of aeration and agitation on microorganism growth, and culture and induction times were evaluated. The highest enzyme activity levels at shake scale were observed in 12 h culture after 2-4 h induction. At bench scale the highest enzyme activity levels were observed after 2 h induction. rGALNS amounts in inclusion bodies fraction were up to 17-fold higher than those observed in the soluble fraction. However, the highest levels of active enzyme were found in the soluble fraction. Western blot analysis showed the presence of a 50-kDa band, in both soluble and inclusion bodies fractions. These results show for the first time the feasibility and potential of production of active rGALNS in a prokaryotic system for development of enzyme replacement therapy for MPS IVA disease.
AB - Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive disorder caused by N-acetylgalactosamine-6-sulfate sulfatase (GALNS) deficiency. Currently no effective therapies exist for MPS IVA. In this work, production of a recombinant GALNS enzyme (rGALNS) in Escherichia coli BL21 strain was studied. At shake scale, the effect of glucose concentration on microorganism growth, and microorganism culture and induction times on rGALNS production were evaluated. At bench scale, the effect of aeration and agitation on microorganism growth, and culture and induction times were evaluated. The highest enzyme activity levels at shake scale were observed in 12 h culture after 2-4 h induction. At bench scale the highest enzyme activity levels were observed after 2 h induction. rGALNS amounts in inclusion bodies fraction were up to 17-fold higher than those observed in the soluble fraction. However, the highest levels of active enzyme were found in the soluble fraction. Western blot analysis showed the presence of a 50-kDa band, in both soluble and inclusion bodies fractions. These results show for the first time the feasibility and potential of production of active rGALNS in a prokaryotic system for development of enzyme replacement therapy for MPS IVA disease.
KW - Escherichia coli BL21
KW - Morquio A disease
KW - N-acetylgalactosamine-6-sulfate sulfatase
KW - Recombinant enzyme
UR - http://www.scopus.com/inward/record.url?scp=78149408453&partnerID=8YFLogxK
U2 - 10.1007/s10295-010-0766-x
DO - 10.1007/s10295-010-0766-x
M3 - Article
C2 - 20582614
AN - SCOPUS:78149408453
SN - 1367-5435
VL - 37
SP - 1193
EP - 1201
JO - Journal of Industrial Microbiology and Biotechnology
JF - Journal of Industrial Microbiology and Biotechnology
IS - 11
ER -