Production of vitamin B12 in escheria coli

Slides:



Advertisements
Similar presentations
Transformation and Cloning
Advertisements

Biotechnology Part II. Genetic Engineering and Recombinant DNA.
Key Area : Genetic Control of Metabolism in Micro-organisms Unit 2: Metabolism and Survival.
Production of the Antimalarial Drug Precursor Artemisinic Acid in Engineered Yeast February 12, 2007 Patrick Gildea By J.D. Keasling et all.
13 The Genetics of Viruses and Prokaryotes. 13 The Genetics of Viruses and Prokaryotes 13.1 How Do Viruses Reproduce and Transmit Genes? 13.2 How Is Gene.
Four of the many different types of human cells: They all share the same genome. What makes them different?
3.1 An overview of genetic possesses 3.2 The basis of hereditary 3.3 DNA replication 3.4 RNA and protein synthesis 3.5 Gene expression.
CHAPTER 31 Genetic Engineering and Biotechnology.
General Microbiology (Micr300) Lecture 11 Biotechnology (Text Chapters: ; )
General Microbiology (MICR300)
Engineering of E.coli for production of poly(3-hydroxypropionate)
16.1 – Producing DNA Fragments. Genetic Engineering Genetic engineering is a rapidly advancing field of Biology. We can now manipulate, alter and even.
Synthetic biology Genome engineering Chris Yellman, U. Texas CSSB.
Center for Biological Sequence Analysis The Technical University of Denmark DTU Comparative Microbial Genomics group Towards a “Systems Microbiology” of.
12.4 Gene Regulation and Mutation
GFP Transformation Lab Images taken without permission from
AP Biology Chapter 18. I can describe how genetic variation occurs in bacteria.
Tissue Culture Unit one Cell and Molecular Biology Advanced Higher Biology.
Definition of Biotechnology in Canadian Legislation Biotechnology is the application of science and engineering in the direct or indirect use of living.
Biotechnology pp WHAT IS IT?  Biotechnology : the application of technology to better use DNA and biology.
Regulation of Gene Expression
Improving NADPH availability for natural product biosynthesis in Escherichia coli by metabolic engineering 汇报人:刘巧洁.
Microbial Biotechnology Philadelphia University
 Operon ◦ Inducible and repressible  Promoter  Terminator  Enhancer  Regulatory Gene  Inducer  Repressor  Regulatory Protein/Sequence  Positive.
Anticipatory Questions
1 Departament of Bioengineering, University of California 2 Harvard Medical School Department of Genetics Metabolic Flux Balance Analysis and the in Silico.
Trp Operon A brief description. Introduction a repressible system In this system, though, unlike the lac operon, the gene for the repressor is not adjacent.
Agenda: 5/20 Tools of Genetics: Restriction Enzymes, Recombinant DNA (Genetic Engineering) Recombinant DNA (Genetic Engineering) What, why, how Reading-
Chapter 12 Lecture Outline Molecular Techniques and Biotechnology.
How Does A Cell Know? Which Gene To Express Which Gene To Express& Which Gene Should Stay Silent? Which Gene Should Stay Silent?
Gene Regulation II : The Ribosome Strikes Back!. Mechanisms Covered Attenuation Control –Tryptophan Biosynthesis Riboswitches –Tryptophan Biosynthesis.
Recombinant DNA What is the basis of recombinant DNA technology? How does one “clone” a gene? How are genetically modified organisms (GMOs) created? Illustration.
1 From Mendel to Genomics Historically –Identify or create mutations, follow inheritance –Determine linkage, create maps Now: Genomics –Not just a gene,
Genetic Engineering Genetic engineering is also referred to as recombinant DNA technology – new combinations of genetic material are produced by artificially.
Regulation of Gene Expression
Microbial Genetics. DNA is the Genetic Material Griffiths Avery et al.
Genetic Transformation of Bacteria and Gene Regulation.
Biosynthesis of Vitamin B 12 Osnaider Gómez Mejía Maitreyi Sadanand Joshi.
 Naturally occurs in cells  Scientists use cell cultures as a source of DNA  Different types of cells are grown in mediums  Cell cultures are collected.
Metabolism - Chapter 5 5 tasks: 1.Bringing nutrients into the cell 2.Breakdown nutrients into useable forms - catabolism 3.Make the building blocks the.
6D – Recognize that a gene expression is a regulated process.
PURINE BIOSYNTHESIS.
Chapter 8, part B Microbial Genetics.
Chapter 8, part B Microbial Genetics.
E.Coli AS MODERN VECTOR.
Genome-wide Responses to Mitochondrial Dysfunction
(Regulation of gene expression)
5. Metabolic Engineering of Bacteria for Food Ingredients
6D – Recognize that a gene expression is a regulated process.
Restriction endonucleases and small biological molecules
Biology lecture 1 The E.coli Cell Gene expression Feedback And Control
applications Agriculture
Genetic Transformation of Bacteria and Gene Regulation
Protein Accounting in the Cellular Economy
Gene Regulation.
Regulation of Gene Expression
Ch 18: Regulation of Gene Expression
Biotechnology and Genetic Engineering PBIO 450/550
Department of Chemical Engineering
Protein Accounting in the Cellular Economy
Technical Solutions The Final Results
Benjamin N. Mijts, Pyung Cheon Lee, Claudia Schmidt-Dannert 
Sensing the Right Time to Be Productive
Discoveries of Nicotinamide Riboside as a Nutrient and Conserved NRK Genes Establish a Preiss-Handler Independent Route to NAD+ in Fungi and Humans  Pawel.
Metabolism and Survival
Selective Breeding and Transgenics
Metabolism and Survival
Chapter 8, part B Microbial Genetics.
E.Coli AS MODERN VECTOR.
Tipping the Energy Balance toward Longevity
Presentation transcript:

Production of vitamin B12 in escheria coli Ida Ruuth

Production of vitamin B12 Vitamin B12 is widely used in medical industry and food industry Need for large scale industrial production Usually produced by Pseudomonas denitrificans, Propionibacterium shermanii, or Sinorhizobium meliloti Long fermentation cycles, complex and expensive media requirements and lack of suitable genetic systems for strain engineering

E. coli Fast growing, no expensive or complex media requirements Well-known Easy to modify genetically Has ability to produce ALA via C5 pathway Precursor for vitamin B12  E. coli lacks about 20 genes required to synthesize the central ring structure of vitamin B12   Has no ability to synthesize vitamin B12 compounds de novo

Pathway of adenosylcobalamin Complex pathway Fusion enzyme CysG is shared between cobalamin and siroheme synthesis. Cobalamin riboswitches regulate cobalamin biosynthesis and transportation at the transcriptional or translational level  btuB gene of E. coli 

Production of vitamin B12 in E.coli More effective ALA supply Expression of HemA from R. palustris Building biosynthetic pathway by using pathway tuning and functional components Genes involved in B12 vitamin pathway into E. coli from S. typhimurium Optimization of pathways Regulation btuB gene

Challenges and Problems How introduced genes function in E. coli Complex pathway and complex structure of vitamin B12 Balance of expressed genes and enzymes Challenges in expressing a great amount of recombinant genes More than 20 genes are involved Balanced supply of precursors

Previous studies Expression of the operon pduBAF-pocR-cbiABCDETFGHJKLMNQOP- cobUST from S. typhimurium into E. coli strain  de novo cobalamin biosynthesis  By Ko et al. twenty-two were cloned via restriction and ligation into three compatible plasmids under the control of a T7 promoter and introduced into E. coli strain.  Vitamin B12 was produced de novo under both anaerobic and aerobic conditions

References Dmitry A. Rodionov et al. 2003. Comparative Genomics of the Vitamin B12 Metabolism and Regulation in Prokaryotes. The Journal of Biological Chemistry. 278, 41148-41159. DOI: 10.1074/jbc.M305837200 Huan Fang et al. 2016.Microbial production of vitamin B12: a review and future perspectives. Microbial Cell Factories. DOI: 10.1186/s12934-017-0631-y Zhang, L., Chen, J., Chen, N. et al. 2013. Cloning of two 5-aminolevulinic acid synthase isozymes HemA and HemO from Rhodopseudomonas palustris with favorable characteristics for 5-aminolevulinic acid production. Biotechnol Lett. 35: 763. doi:10.1007/s10529-013-1143-4