Batch sterilization Most nutrient media are presently sterilized in batch volumes in the bioreactor at 121°C. Approximate sterilization times can be calculatee.

Slides:



Advertisements
Similar presentations
Heat Transfer in Fermentation
Advertisements

Culturing Microbes.
Dynamic Energy Balance. Last time: well-mixed CSTR w/flow & reaction for multiple reactions: rxn #
Fermentation Technology
STERILISATION (PAGE 371, Doran e-book).
How To Prepare, Sterilize, AND Test Culture Media
By: Mdm. Noor Amirah Abdul Halim BIOREACTION AND BIOREACTOR.
Example 1 - Superheat Rankine Cycle
Drug Delivery & Tissue Engineering Laboratory
Lauren O’Brien, Adrienne Campbell, Lewis Reis, Paul Stewart.
Wed Lab 5 discussion: Discuss aseptic technique and better ways/equipment for sampling. 5 minutes to look at plates Lecture continued Worksheet.
Biology 3A.
Growth curves of micro-organisms. Learning Objectives  Discuss the growth curves of micro organisms  Outline the differences between batch and continuous.
Biotechnology practical course Second Year Clinical.
Enzymes And how they work.
Industrial Biotechnology
Micro Practical 3 PRINCIPLE AND WORKING OF AUTOCLAVE Dr. Shahzad Ali Assistant Professor Department of Wildlife and Ecology UVAS, Ravi Campus, Pattoki.
Culture Media Lab 2:.
Media Preparation & Sterilization
Sterilization Lecture 7 Tahir.
Cells Growth in Continuous Culture Continuous culture: fresh nutrient medium is continually supplied to a well-stirred culture and products and cells are.
High temperature methods
Biotechnology basics State that biotechnology is the industrial use of living organisms (or parts of them) to produce food, drugs or other products. What.
BASIC MICROBIOLOGY.
Chapter 7: STERILIZATION
What is plasma? Plasma is an ionized gas comprising molecules,atoms, ions ( in their ground or excited states) electrons and photons. It is electrically.
Sterilization CP504 – ppt_Set 09
Sterilization CP504 – Lecture 15 and 16
Heat: Phase Change. 'change of phase' 'change of state'. The term 'change of phase' means the same thing as the term 'change of state'. o These changes.
Phase changes Melting solid  liquid Freezing liquid  solid
Microbial Biotechnology Commercial Production of Microorganism
Industrial Microorganisms and Product Formation
Lab 2: Culture Media. In this lab we learn about different types of media that are used to grow bacteria. Some types of media will grow just about any.
FERMENTATION.
D ESCRIBE THE BIOREACTOR PARAMETERS AND HOW TO CONTROL THE TEMPERATURE.
FERMENTATION.
Heating Curves. Energy and Phase Change When adding heat to a solid, energy added increases the temperature and entropy until the melting point is reached.
By, Kaya Zepeda, Joselyne Soto, Greg Maginn, Sebastian Hickey, and Chase Lewis.
Microbiology / Lab. 8. o Culture (Growth) Media I.What is a medium (plural media)? II.What is culture medium? III.What is meant by Inoculation of Media?
Batch Growth Kinetics Heat generation by microbial growth
A Watched Cup Never Cools Class Project  When you have a hot cup of coffee, how long does it take until the liquid in the cup reaches room temperature?
Immobilized Cell System
Sterilization: concept and methods
CHAPTER 4.2 Convection and the Mantle. Standard  S.6.4.c Students know heat from Earth’s interior reaches the surface primarily through convection.
Microbial growth in:- Closed Cultivation Systems Open Cultivation Systems Semi-Open Cultivation Systems.
Fermentation control and monitoring Dr Imran. What we want to control primarily aeration, mixing, temperature, pH and foam control These depend on 1-
Fermentation Technology
Class 20 Scaleup Book Chapter 10 It seems insignificant but there is a general chemical rule that says each 10x scale up of the batch size takes as much.
Measurement of Heat Energy. The amount of heat given off or absorbed in a reaction can be calculated by a) q=mc∆T(Table T) q= heat (in joules or calories)
ASEPTIC TECHNIQUE.  Laboratory practices that minimize the risk of cultured cells becoming contaminated with unwanted microorganisms.
Laboratory equipment Lecture (5).
Fermentation.
DESIGN OF CONTINUOUS STERILIZATION PROCESSES
Lab session 1.
Thermodynamics Processes.
Steam Engine Sliding valve Steam enters chamber from
INDUSTRIAL MICROBIOLOGY Dr. TERESA FERNÁNDEZ ALDAMA
Micro-organisms understand the role of yeast in the production of beer
1. Microorganisms require about 10 elements in large quantities for the synthesis of macromolecules. State clearly all the elements. [10 marks] 2. Describe.
The Basic Direct Expansion Refrigeration Cycle
Growth curves of micro-organisms
Growth & Metabolism of Micro-organisms
Bioreactors Engineering
Basis Operations in Industrial Fermentations
Kinetics of thermal death of microorganisms
Culture Media Lab 2:.
4. Basis Operations in Food Fermentations (Biotechnology)
Bioprocess and engineering presentation Effect of activation energy on thermal destruction of media nutrients & designed organism.
Growth curves of micro-organisms
Laboratory equipment Lecture (9).
Presentation transcript:

Batch sterilization Most nutrient media are presently sterilized in batch volumes in the bioreactor at 121°C. Approximate sterilization times can be calculatee from the nature of the medium and the size

Not only the nutrient media, but also the fittings, valves and electrodes of the fer-menter itself must be sterilized. Therefore, actual sterilization times are significantly longer than calculated ones and must be empirically deter-mined for the specific nutrient solutions in thefermenter. ·One method of sterilization is to injecting n into the fermenter mantle or interior coils red sterilization. ·Another method is to inject steam into the nutrient solution itself. With direct steam injection, condensate accumulates in the fermenter and the volume of liquid increases during the sterilization process.

Another method is to inject steam into the nutrient solution itself. With direct steam injection, condensate accumulates in the fermenter and the volume of liquid increases during the sterilization process.

It takes 2-3 s to reach the sterilization temperature of 1210C. depending on the steam conduction and enter size. Once the proper temperature has, reached, another minutes are required for the actual killing process, followed by cooling for about one hour.

Another disadvantage of heat sterilization (and from the standpoint of microbiology the most significant shortcoming) is that heating, sterilization and cooling phases not only kill microorganisms but also se-verely alter nutrient solutions. Discoloration and changes in the pH value result from caramelization and Maillard reactions. Vitamins are destroyed and the quality of the culture medium deteriorates. The extent to which the subsequent fermentation is affected depends on the organism and the process.