Biochemical Engineering
Code: 106062 ECTS Credits: 6| Degree | Type | Year |
|---|---|---|
| 2500897 Chemical Engineering | OT | 4 |
Contact
- Name:
- José Luis Montesinos Seguí
- Email:
- joseluis.montesinos@uab.cat
Teaching groups languages
You can view this information at the end of this document.
Prerequisites
It is recommended having reached the basic knowledge on: Biology and General Biochemistry, Reactors, Computer Applications and Simulation of Chemical Processes.
Objectives and Contextualisation
To relate and apply known concepts and methods in different subjects (from biology and biochemistry to the fundamental principles of chemical engineering) in the analysis and design of bioprocesses: how, when and where to apply the knowledge acquired. For this, basic knowledge must be achieved, know how to apply it and solve problems on different relevant aspects in bioindustrial processes, such as mass and energy balances, transport phenomena, design and proper use of a bioreactor according to its application, as well as the interaction between kinetics and operational mode. Finally, it is necessary to know how to correctly describe and design the variety of separation processes at different scales in the field of bioprocesses.
Competences
- Apply scientific method to systems in which chemical, physical or biological transformations are produced both on a microscopic and macroscopic scale.
- Demonstrate knowledge of the different reaction, separation and processing operations for materials, and transport and circulation of fluids involved in the industrial processes of chemical engineering.
- Develop personal work habits.
- Understand and apply the basic principles on which chemical engineering is founded, and more precisely: balances of matter, energy and thermodynamic momentum, phase equilibrium and kinetic chemical equilibrium of the physical processes of matter, energy and momentum transfer, and kinetics of chemical reactions
- Work in a team.
Learning Outcomes
- Describe the interaction between kinetics and bioreactor operation mode.
- Develop independent learning strategies.
- Efficiently translate the findings of basic biological research into engineering applications for society.
- Explain, apply and resolve problems regarding matter and energy balance in bioindustrial processes.
- Identify and apply immobilisation systems and their operation modes.
- Objectively select alternatives in consideration of performance parameters, selectivity and economic criteria.
- Work cooperatively.
Content
TOPIC 1.- BIOCHEMICAL ENGINEERING AND BIOTECNOLOGY
1.1. Introduction to Biotechnological Processes. Involved sectors
1.2. Biochemical Engineering
1.3. Applications of enzymes, microorganisms and cells. New products
1.4. Fermentation
TOPIC 2.- ENZYMES. KINETICS AND APPLICATION
2.1. Introduction to enzymatic catalysis
2.2. Classification of enzymes
2.3. Enzyme kinetics
2.3.1. Enzymatic reactions with one substrate
2.3.2. Michaelis-Menten equation
2.3.3. Determination of kinetic parameters
2.3.4. Enzymatic reactions with inhibition
2.3.5. Factors that influence activity and enzymatic stability
2.4. Use and application of enzymes
TOPIC 3.- CELULAR GROWTH
3.1. Phases of cell culture
3.2. Growth kinetics. Models
3.3. Effects of culture conditions in growth kinetics
3.4. Determination of cell density
3.5. Culture media and cell composition
TOPIC 4.- MASS AND ENERGY BALANCES
4.1. Cell growth, substrate uptake and product formation
4.2. Stoichiometry of the system
4.3. Yields
4.4. Mass and energy balances
4.4.1. Substrate as energy source. Intrinsic yield and maintenance coefficient
4.4.2. Elemental balances
4.4.3. Redox balance. Degree of reduction
TOPIC 5.- IMMOBILIZED BIOCATALYSTS
5.1. General concepts
5.1.1. Immobilization methods
5.1.2. Adsorption
5.1.3. Covalent chain
5.1.4. Cross-linking
5.1.5. Entrapment
5.1.6. Membranes
5.2. Selection of immobilization method
5.3. Kinetics of immobilized biocatalysts
5.3.1. External mass transfer
5.3.2. Internal mass transfer
5.4. Application of immobilized biocatalysts
TOPIC 6.- DESIGN OF IDEAL BIOREACTORS
6.1. Cell reactors
6.1.1. Batch reactor
6.1.2. Fed-batch reactor
6.1.3. CSTR
6.1.4. CSTR’s in Series
6.1.5. CSTR with Recirculation
6.1.6. PFR
6.2. Enzyme reactors
6.2.1. Batch reactor
6.2.2. CSTR
6.2.3. PFR
TOPIC 7.- AERATION
7.1. Oxygen transfer rate (OTR)
7.2. Factors that influence the oxygen transfer rate
7.3. Oxygen uptake rate (OUR)
7.4. Experimental determination of kLa coefficient
7.4.1. Indirect methods
7.4.2. Direct methods
TOPIC 8.- AGITATION
8.1. Fermentation-broth rheology
8.2. Factors and effects of shear stress
8.3. Design of agitation systems
8.3.1. Type of Agitators
8.3.2. Agitator power requirements
8.4. Estimation of kLa coefficient inaerated systems
TOPIC 9.- STERILIZATION
9.1. Introduction and objectives
9.2. Physical methods of sterilization
9.2.1. Thermal treatments
9.2.2. Sterilization of gases
9.3. Chemical treatments
9.4. Other methods for microorganism control
TOPIC 10.- BIOREACTOR CONFIGURATION AND OPERATION
10.1. Configuration and elements of the different type of bioreactor
10.2. Bioreactor operation. Instrumentation and control
10.2.1. Fermenters
10.2.2. Cell culture
10.3. Scale-up
10.3.1. Theory of similarity
10.3.2. Most commonly applied methods
TOPIC 11.- SEPARATION AND RECOVERY OF PRODUCTS
11.1. Introduction to downstream processing in bioprocesses
11.2. Separation sequence
11.3. Separation of insoluble products
11.4. Cell disruption
11.5. Separation of soluble products
11.6. Examples in different bioprocesses
Activities and Methodology
| Title | Hours | ECTS | Learning Outcomes |
|---|---|---|---|
| Type: Directed | |||
| Classroom practices (Problem solving) | 15 | 0.6 | 1, 2, 3, 4, 5, 6, 7 |
| Expository lectures (master class) | 30 | 1.2 | 1, 2, 3, 4, 5, 6 |
| Seminars | 5 | 0.2 | 1, 3, 6 |
| Type: Supervised | |||
| Further tutorials | 3 | 0.12 | 1, 2, 3, 4, 5, 6, 7 |
| Type: Autonomous | |||
| Problem solving | 50 | 2 | 1, 2, 3, 4, 5, 6, 7 |
| Study | 38 | 1.52 | 1, 2, 3, 4, 5, 6, 7 |
| Tutorials with professor | 2 | 0.08 | 1, 2, 3, 4, 5, 6, 7 |
MD1 Presentation of content in class – Master class or conference
MD2 Participatory classes (joint problem solving, debates, case analysis, presentations of work done by students)
MD3 Tutorials
MD5 Evaluation activities (continuous evaluation with at least three milestones: Initial, follow-up and final)
MD6 Problem/use case/project based learning
Annotation: Within the schedule set by the centre or degree programme, 15 minutes of one class will be reserved for students to evaluate their lecturers and their courses or modules through questionnaires.
Assessment
Continous Assessment Activities
| Title | Weighting | Hours | ECTS | Learning Outcomes |
|---|---|---|---|---|
| Delivery and presentation of problems, activities and exercises | 20 % | 0 | 0 | 1, 2, 3, 4, 5, 6, 7 |
| Partial tests | 30 % | 2 | 0.08 | 1, 2, 3, 4, 5, 6 |
| Synthesis test | 50 % | 5 | 0.2 | 1, 2, 3, 4, 5, 6 |
To consider the subject passed, it will be necessary to obtain a minimum overall mark of 50/100.
a) Evaluation process and programmed activities
The continuous evaluation will be made considering a series of tests and activities:
• Problems, tasks, and exercises (PTE): 20 % of the final course mark.
• 1st partial test (PP1)) (topics 1 to 5): 15 % of the final course mark.
• 2nd partial test (PP2) (topics 6 to10): 15 % of the final course mark.
• Synthesis test (PS) (topics 1 to 11): 50 % of the final course mark.
The problems, tasks, and exercises (PTE) will be done individually or in groups and may or may not be problems from the subject list, specific study cases and activities based on key theoretical concepts of the corresponding topics.
The partial tests (PP1, PP2) will consist of a short problem and theoretical concepts of the corresponding topics (1h). The synthesis test (PS) will include all the content of the subject and will consist of a theoretical part and another with three problems (4h).
In the partial tests and the problems of the synthesis test, support material can be used: notes, books, forms, solved problems, computer, calculation tools, etc. In the theory part of the synthesis test no type of additional material may be used unless indicated by the teacher.
b) Time-scheduling of evaluation activities
The time-schedule of the evaluation and delivery of work activities will be published in the corresponding virtual platform (Moodle) and may be subject to possible programming changes for reasons of adaptation to possible incidents. Always being informed in the corresponding virtual Platform about these changes, since it is understood that this is the usual platform for exchange of information between teachers and students.
Tests will not be held on dates, times, and places other than those scheduled and disseminated by the Degree Coordination/School of Engineering. No change may be introduced without the approval of the degree coordination. After 30 minutes of the scheduled time of the evaluation activity, if it has not started, it will be cancelled. Canceled activities will be rescheduled.
c) Recovery process
Students who have failed the continuous evaluation or want to raise the mark will be able to take the final recovery test (PR 100%). They must have been evaluated from a set of activities that represents a minimum of 2/3 parts of the total subject qualification. By taking this final recovery test, they waive all the marks of the continuous evaluation.
The final test will include all the content of the subject and will consist of a theoretical part and another with two problems (4h). In the problems of the final test, supporting material can be used: notes, books, forms, solved problems, computer, calculation tools, etc. In the theory part of the final test no type of additional material can be used unless indicated by the teacher. In case of not taking the final test, the final course mark for the subject will be the obtained from the continuous evaluation.
d) Revision of the qualifications
For each evaluation activity, a place, date, and time of review will be indicated at the corresponding virtual platform (Moodle) in which the student can review the activity with the teacher.
e) Special qualifications
Granting a qualification of “matrícula de honor” (MH), apart from the minimum mark that can give access (≥ 9.00), is the decision of the faculty responsible for the course that will take into account the proactivity towards the subject, the understanding of the fundamentals and their relationship with other subjects and the fluency, reliability, expression and rational thinking. Special attention will be paid to the theoretical part of the synthesis and final tests. The MH resulting from calculating the 5% or fraction of people enrolled may be granted. Students will be considered Not Evaluable (NA) if have not been evaluated from a set of activities that represents a minimum of 2/3 parts of the total subject qualification.
f) Irregularities from the student, copying and plagiarism
If the student performs any irregularity that may lead to a significant variation in the grade of an evaluation act, this evaluation act will be graded with a 0, regardless of the disciplinary process that may be instructed. This evaluation activity will not be recoverable. The professor responsible for the subject will have to report these cases to the coordination of the degree that will record the fact.
g) Second registration or more
From the second registration, the student could choose between new continuous evaluation or a synthesis test that will be the same test (equal date and time) as the synthesis test (PS) for the students of first registration. It is mandatory to be communicated by e-mail to the teacher within the first 15 days of the course. Thus, the qualification of the course will correspond either to the continuous evaluation or just the mark of this test (PS 100%), replacing the continuous evaluation for all purposes. They could also do a final recovery test (PR 100%), according to requirements and conditions for the modality selected, and will be the same test (equal date and time) than the recovery test (PR 100%) for the students of first registration.
h) Single evaluation
This subject does not provide for a single evaluation system.
Bibliography
- Berenjian, A. Essentials in Fermentation Technology. Springer. (2019). Digital version.
- Blanch, H.W., Clark, D.S. Biochemical Engineering. Marcel Dekker. (1997).
- Doran, P.M. Bioprocess Engineering Principles, 2nd ed. Academic Press. 2n ed. (2013). Digital version.
- El-Mansi, EMT, Bryce, C.F.A., Demain, A.L., Allman, A.R. Fermentation Microbiology and Biotechnology, 3rd ed. CRC Press. (2011).
- Gòdia, F., López, J. Ingeniería Bioquímica. Síntesis. (1998).
- Liu, Sh. Bioprocess Engineering. Kinetics, Sustainability, and Reactor Design. Elsevier B.V. 2n ed. (2017). Digital version.
- Shuler, M.L., Kargi, F., De Lisa, M. Bioprocess engineering: basic concepts. Prentice Hall PTR. 3rd ed. (2017).
Software
- Pal, Nirupam & Siletti, Charles & Petrides, Demetri. (2008). Superpro Designer: An Interactive Software Tool for Designing and Evaluating Integrated Chemical, Biochemical, and Environmental Processes.
Language list
| Name | Group | Language | Semester | Turn |
|---|---|---|---|---|
| (PAUL) Classroom practices | 1 | Catalan/Spanish | first semester | morning-mixed |
| (SEM) Seminars | 1 | Catalan/Spanish | first semester | morning-mixed |
| (TE) Theory | 1 | Catalan/Spanish | first semester | morning-mixed |