A New Method for Production of Combinatorial Libraries by Mating of Saccharomyces cerevisiae Cells
スポンサーリンク
概要
- 論文の詳細を見る
There are two kinds of mating types in yeast cells, a-type and α-type, and they can make a diploid, which carries both the genes originated from a-type and α-type. We propose a new method to obtain a larger size of combinatorial libraries by mating these yeast cells. By transforming libraries of genes of heavy and light chains to a- and α-types respectively, for example, it should be possible to obtain a larger size of libraries of antibodies by mating them. To confirm our method, the expression vectors containing heavy chain gene (μ) and light chain genes (κ and λ) of human antibodies were transformed into a-type and α-type strains of S. cerevisiae, respectively, and these transformants were mated by mixing the cultured cells of both types. The effects of media, cell concentration and the ratio of a-type cells to α-type cells on the mating efficiency were studied. The direct contact between a- and α-type cells was essential to initiate mating of cells, and the probability of contact among cells determined the mating efficiency, when cells are well nourished. Stable diploids were formed by the combination of plasmids of the 2 μm types, as well as the combination between the 2 μm type and the ARS1 type.
- 社団法人 化学工学会の論文
- 2002-05-01
著者
-
KATOH Shigeo
Graduate School of Science and Technology, Kobe University
-
Shiomi Naofumi
Department of Biosphere Sciences, Kobe College
-
Murao Kenji
Graduate School Of Science And Technology Kobe University
-
Katoh Shigeo
Graduate School Of Engineering Department Of Chemical Science And Engineering Kobe University:depart
-
Shiomi Naofumi
Department Of Biosphere Sciences Kobe College
-
Shiomi N
Department Of Human Sciences Kobe College
-
KOGA Hirohisa
Graduate School of Science and Technology, Kobe University
-
KURODA Kousuke
Graduate School of Science and Technology, Kobe University
-
HOSOKAWA Hiroyo
Graduate School of Science and Technology, Kobe University
-
Koga Hirohisa
Graduate School Of Science And Technology Kobe University
-
Kuroda Kousuke
Graduate School Of Science And Technology Kobe University
-
Hosokawa Hiroyo
Graduate School Of Science And Technology Kobe University
関連論文
- Liposome Immune Lysis Assay of Antibodies by Liposomes Encapsulating Coenzyme β-NAD^+
- Production of Single-Chain Variable Fragment Antibody (scFv) in Fed-Batch and Continuous Culture of Pichia pastoris by Two Different Methanol Feeding Methods(BIOCHEMICAL ENGINEERING)
- Effects of Methanol Feeding Methods on Chimeric α-Amylase Expression in Continuous Culture of Pichia pastoris(BIOCHEMICAL ENGINEERING)
- Degradation of Cyanuric Acid in Soil by Pseudomonas sp. NRRL B-12227 Using Bioremediation with Self-Immobilization System(ENVIRONMENTAL BIOTECHNOLOGY)
- Neutralization of Acids by Microorganisms Co-Immobilized with Bacillus subtilis in a Shallow Layer of Model Soil
- Nucleotide Sequence and Characterization of a Gene Conferring Resistance to Ethionine in Yeast Saccharomyces cerevisiae
- Characteristics of Liposome Immunosorbent Assay (LISA) Using Liposomes Encapsulating Coenzyme β-NAD^+
- Light Attenuation in Suspension of the Purple Bacterium Rhodobacter capsulatus and the Green Alga Chlamydomonas reinhardtii
- High Performance in Protease Refolding by Application of a Continuous System Using Immobilized Inhibitor(BIOCHEMICAL ENGINEERING)
- ACE Inhibitory Activity and Characteristics of Tri-Peptides Obtained from Bonito Protein
- Secretion of α-Amylase from Saccharomyces cerevisiae and Pichia pastoris and Characterization of Its C-Terminus with an Anti-Peptide Antibody
- Characteristics of Neutralization of Acids by Newly Isolated Fungal Cells
- A Bioremediation Method Based on Self-Immobilization of Cells in Shallow Layer of Soil
- Immobilization of Candida Cells Showing Mycelium-Like Shapes in Porous Polyvinyl Formal Resin and Their Applications
- Liposome Immunoblotting Assay Utilizing an Enhanced Chemiluminescent Reaction Improved by Surfactant
- Elution Behavior of DNAs in Temperature-Gradient Affinity Chromatography for Single Nucleotide Polymorphism Detection
- Production of S-Adenosyl-D,L-homocysteine by Saccharomyces cerevisiae Cells Transformed with an Ethionine Resistance Gene(Microbiology & Fermentation Industry)
- Cloning of Genes for Spermine Resistance in Saccharomyces cerevisiae and Their Effects on S-Adenosyl-L-Methionine Accumulation
- Effect of Flashing Light from Blue Light Emitting Diodes on Cell Growth and Astaxanthin Production of Haematococcus pluvialis(BIOCHEMICAL ENGINEERING)
- Effective Utilization of Transmitted Light for Astaxanthin Production by Haematococcus pluvialis(BIOCHEMICAL ENGINEERING)
- Fed-Batch Culture under Illumination with Blue Light Emitting Diodes (LEDs) for Astaxanthin Production by Haematococcus pluvialis(BIOCHEMICAL ENGINEERING)
- Effects of Nutrient Supply Methods and Illumination with Blue Light Emitting Diodes (LEDs) on Astaxanthin Production by Haematococcus pluvialis(BIOCHEMICAL ENGINEERING)
- Characterization of Continuous Refolding Apparatus Using Different Mixing Methods
- Control of Aggregate Formation in Refolding of Carbonic Anhydrase at High Urea Concentrations and Effects of Urea Removal
- High Yield Refolding of Lysozyme and Carbonic Anhydrase at High Protein Concentrations
- Production of Glucoamylase by Passively Immobilized Cells of a Flocculent Yeast, Saccharomyces diastaticus
- Utilization of antipeptide antibodies as affinity ligands in immunoaffinity purification
- A New Method for Production of Combinatorial Libraries by Mating of Saccharomyces cerevisiae Cells
- Improvement of Growth Stability of Photosynthetic Bacterium Phodobacter capsulatus(BIOCHEMICAL ENGINEERING)
- Efficient production of single-chain Fv antibody possessing rare codon linkers in fed-batch fermentation(BIOCHEMICAL ENGINEERING)
- Effect of Nucleotide Sequences of Polypeptide Linkers on Production of Soluble Single-Chain Fv Antibodies
- Epitope Screening by Use of a Random Peptide-Displayed Phage Library and Polyclonal Antibody-Coupled Liposomes
- Characteristics of Microblotting Assay Using Immunoloposomes(BIOCHEMICAL ENGINEERING)