ABSTRACT
OBJECTIVE: To evaluate whether the surface layer (S-layer) protein of Lactobacillus brevis serves as a self-aggregating protein tag for cost-effective separation of human and yeast D-amino acid oxidases (hDAAO and yDAAO) expressed in E. coli. RESULTS: In aqueous two-phase (PEG-phosphate) system, the S-layer:DAAO fusion proteins (shDAAO and syDAAO) were separated at the interface with a recovery of 82 ± 10.6% for shDAAO and 95 ± 1.9% for syDAAO. Some shDAAO proteins were separated as precipitates with a recovery of 41 ± 0.5% in phosphate (9%, w/w) using PEG 3000 and PEG 4000 (16%, w/w), while some syDAAO proteins were also isolated as precipitates with a recovery of 75 ± 17.5% in phosphate (9%, w/w) using PEG 4000 and PEG 8000 (16%, w/w). CONCLUSIONS: The S-layer of L. brevis was applied to a self-assembled protein tag to enable cost-effective separation of human and yeast D-amino acid oxidases expressed in E. coli cells. Because of the self-assembling properties of S-layer proteins, human and yeast D-amino acid oxidases fused with S-layer proteins could be easily separated by aggregates at the interface and/or in a few conditions by precipitates to the bottom of the PEG-phosphate aqueous system.
Subject(s)
D-Amino-Acid Oxidase/isolation & purification , Levilactobacillus brevis/metabolism , Membrane Glycoproteins/metabolism , Recombinant Fusion Proteins/isolation & purification , Chromatography, Affinity/economics , D-Amino-Acid Oxidase/genetics , DEAE-Dextran , Fungal Proteins/isolation & purification , Humans , Membrane Glycoproteins/genetics , Saccharomyces cerevisiae/metabolism , Species SpecificityABSTRACT
A deracemization method was developed to generate optically pure L-homoalanine from racemic homoalanine using D-amino acid oxidase and ω-transaminase. A whole cell reaction using a biphasic system converted 500 mM racemic homoalanine to 485 mM L-homoalanine (>99% ee).
Subject(s)
Aminobutyrates/chemistry , D-Amino-Acid Oxidase/metabolism , Transaminases/metabolism , Aminobutyrates/metabolism , Escherichia coli/chemistry , Escherichia coli/enzymology , Kinetics , StereoisomerismABSTRACT
In this study, a fusion protein (VHb-DAAO) of D-amino acid oxidase (DAAO) with Vitreoscilla hemoglobin (VHb) was functionally expressed in Escherichia coli and purified. The k(cat) value VHb-DAAO (47.1 s⻹) towards rac-3-flouroalanine was about 2-fold higher than that of DAAO (21.9 s⻹). rac-3-Flouroalanine (500 mM) was kinetically resolved into (R)-3-fluoroalanine with high enatiomeric excess (>99%) by VHb-DAAO with about 52% conversion.
Subject(s)
Alanine/analogs & derivatives , Bacterial Proteins/genetics , D-Amino-Acid Oxidase/metabolism , Recombinant Fusion Proteins/metabolism , Truncated Hemoglobins/genetics , Alanine/chemistry , Alanine/isolation & purification , Alanine/metabolism , D-Amino-Acid Oxidase/genetics , D-Amino-Acid Oxidase/isolation & purification , Formate Dehydrogenases/metabolism , Kinetics , NAD/metabolism , Oxidation-Reduction , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/isolation & purification , Rhodotorula/enzymology , StereoisomerismABSTRACT
A chimeric gene encoding enhanced green fluorescent protein (EGFP) and a S-layer protein from Lactobacillus brevis KCTC3102, and/or two copies of the Fc-binding Z-domain, a synthetic analog of the B-domain of protein A, was constructed and expressed in Escherichia coli BL21(DE3). The S-layer fusion proteins produced in a 500-l fermentor were likely to be stable in the range of pH 5 to 8 and 0 degree to 40 degrees . Their adhesive property enabled an easy and rapid immobilization of enzymes or antibodies on solid materials such as plastics, glass, sol-gel films, and intestinal epithelial cells. Owing to their affinity towards intestinal cells and immunoglobulin G, the Slayer fusion proteins enabled the adhesion of antibodies to human epithelial cells. In addition, feeding a mixture of the S-layer fusion proteins and antibodies against neonatal calf diarrhea (coronavirus, rotavirus, Escherichia coli, and Salmonella typhimurium) to Hanwoo calves resulted in 100% prevention of neonatal calf diarrhea syndrome (p<0.01),whereas feeding antibodies only resulted in 56% prevention.
Subject(s)
Antibody Affinity , Cattle Diseases/immunology , Diarrhea/veterinary , Intestinal Mucosa/metabolism , Levilactobacillus brevis/genetics , Membrane Glycoproteins/immunology , Recombinant Fusion Proteins/biosynthesis , Animals , Cattle , Cattle Diseases/metabolism , Cattle Diseases/microbiology , Diarrhea/immunology , Diarrhea/microbiology , Epithelial Cells/immunology , Epithelial Cells/metabolism , Green Fluorescent Proteins , Humans , Immunoglobulin Fc Fragments/biosynthesis , Immunoglobulin Fc Fragments/genetics , Immunoglobulin Fc Fragments/immunology , Intestines/immunology , Membrane Glycoproteins/biosynthesis , Membrane Glycoproteins/genetics , Mice , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/immunology , Staphylococcal Protein A/biosynthesis , Staphylococcal Protein A/genetics , Staphylococcal Protein A/immunologyABSTRACT
The PepQ prolidase from Escherichia coli catalyzes the hydrolysis of dipeptide substrates with a proline residue at the C-terminus. The pepQ gene has been cloned, overexpressed, and the enzyme purified to homogeneity. The k(cat) and k(cat)/K(m) values for the hydrolysis of Met-Pro are 109 s(-1) and 8.4 x 10(5)M(-1)s(-1), respectively. The enzyme also catalyzes the stereoselective hydrolysis of organophosphate triesters and organophosphonate diesters. A series of 16 organophosphate triesters with a p-nitrophenyl leaving group were assessed as substrates for PepQ. The S(P)-enantiomer of methyl phenyl p-nitrophenyl phosphate was hydrolyzed with a k(cat) of 36 min(-1) and a k(cat)/K(m) of 710 M(-1)s(-1). The corresponding R(P)-enantiomer was hydrolyzed more slowly with a k(cat) of 0.4 min(-1) and a k(cat)/K(m) of 11 M(-1)s(-1). The PepQ prolidase can be utilized for the kinetic resolution of racemic phosphate esters. The PepQ prolidase was shown to hydrolyze the p-nitrophenyl analogs of the nerve agents GB (sarin), GD (soman), GF, and VX.
Subject(s)
Dipeptidases/metabolism , Escherichia coli/enzymology , Base Sequence , Catalysis , Cloning, Molecular , DNA Primers , Dipeptidases/genetics , Escherichia coli/genetics , Genes, Bacterial , HydrolysisABSTRACT
In this study we constructed an artificial flavohemoprotein by fusing Vitreoscilla hemoglobin (VHb) with D-amino acid oxidase (DAO) of Rhodotorula gracilis to determine whether bacterial hemoglobin can be used as an oxygen donor to immobilized flavoenzyme. This chimeric enzyme significantly enhanced DAO activity and stability in the bioconversion process of cephalosporin C. In a 200-mL bioreactor, the catalytic efficiency of immobilized VHb-DAO against cephalosporin C was 12.5-fold higher than that of immobilized DAO, and the operational stability of the immobilized VHb-DAO was approximately threefold better than that of the immobilized DAO. In the scaled-up bioprocess with a 5-L bioreactor, immobilized VHb-DAO (2500 U/L) resulted in 99% bioconversion of 120 mM cephalosporin C within 60 min at an oxygen flow rate of 0.2 (v/v) x min. Ninety percent of the initial activity of immobilized VHb-DAO could be maintained at up to 50 cycles of the enzymatic reaction without exogenous addition of H(2)O(2) and flavin adenine dinucleotide (FAD). The purity of the final product, glutaryl-7-aminocephalosporanic acid, was confirmed to be 99.77% by high-performance liquid chromatography (HPLC) analysis. Relative specificity of immobilized VHb-DAO on D-alpha-aminoadipic acid, a precursor in cephalosporin C biosynthesis, increased twofold, compared with that of immobilized DAO, suggesting that conformational modification of the VHb-DAO fusion protein may be altered in favor of cephalosporin C.