2. Capaian Pembelajaran Mata Kuliah (CPMK)
Setelah mengikuti perkuliahan Pengantar Bioproses ini,
mahasiswa akan mampu mendefinisikan dan
merencanakan konsep bioproses dan aplikasi bioproses dalam
proses Industri serta mampu memahami dan menggambar
kurva pertumbuhan mikroorganisme
3. Sub-CPMK
Sub-CPMK1:
Mahasiswa akan mampu mengidentifikasi dan menjelaskan
pengertian dan konsep Bioproses, apa kaitannya dengan disiplin
Ilmu Teknik Kimia, bagaimana aplikasinya dalam proses industri, dan
persiapan media pertumbuhan mikroorganisme dalam bioproses
4. Objective
1. Study aspects, scope, performance, and application of
bioprocess
2. Preparation of microbial growth media
3. Curve of microbial growth
4. Measurement and calculation of the number of microbes
5. Reference
1. Ketchum, P., Microbiology: Concepts and Application, John Wiley & Sons, New York, 1988.
2. D. Dwijosaputro. Dasar-dasar Mikrobiologi. Penerbit Djambatan 1990.
3. Krueger, et al., Introduction to Microbiology, Mc Millan, 1979.
4. Frosbisher, et al., Fundamental of Microbiology, Saunders (Toppan), 1974
5. Bailey dan Ollis. Biochemical Engineering Fundamentals, Mc Graw Hill, 1987
6. Aiba, et al., Biochemical Engineering, Tokyo University Press, 1973
7. Cooney, Fermentation and Enzyme Technology, John Wiley, 1973
8. Wang, D.C., Cooney, C.L., Dunnill, P., Humphrey, A.E., & Lilly. M.D. Fermentation and Enzyme
Technology. John Wiley & Sons, Singapore, 1979.
6. Schedule and evaluation assessment
Schedule :
• Class A and C : Wed, 1.00 – 2.10 p.m
• Class B and D : Wed, 8.00 – 9.10 a.m
Evaluation assessment
Evaluation Assessment is carried out on each learning achievement with details:
- Problem Based Learning (individual ass)
- Tasks (ind/grup)
- Ujian Pengukuran CP
7. What do you think about
BIOPROCESS ?
Short Quiz
9. BIOPROCESS
A combination of biotechnology and chemical engineering
The branch of science of chemical engineering that deals
with the design and construction of production processes
involving biological agents. Biological agents can be
microorganisms or enzymes produced by microorganisms.
13. Physiology: cell
processes and
activities of an
organism
02
Biochemistry:
chemical reactions
and processes in
cells
03
Genetics: the
genetic material
in cells
04
Microbiology:
understanding of
microbes (types,
structures and
components of cells)
01
Bioprocess needs research assistance
14. Microbes in bioprocess
simple genetic material
Reproduction is rapid
The size is small, so
the ratio of area to cell
volume is high
relatively does not
produce toxic waste
(safe for the
environment)
Can grow on a variety
of media
15. What is a BIOPROCESSENGINEER??
Technically trained to understand, design, and
efficiently handle bioreactors.
Ensures that a favorable sustainable state or
predictable outcome of a bioprocess is achieved
Differentiating from other engineers, training in
biological sciences, especially quantitative and
analytical biological sciences, and green chemistry
17. Bioprocess applications and products
01 Medical field:
02
biopesticides, animal feed, xylase enzymes,
compost and fertilizers, Nitrogen fixing bacteria etc..
Agriculture:
03 Chemical Industry
antibiotics, vaccines, vitamins, steroids, hormones,
antibodies, interferons etc.
Ethanol, acetone, butanol, organic acids,
biopolymers, surfactants, perfumes etc.
04
Alcoholic beverages, fermented dairy products, PST,
organic acids, enzymes, antioxidants, sweetening
agents, dyes, aromas, etc.
Agroindustry :
18. Enzymatic
Feedstock Bioprocessing Product
GAS
LIQUID
SOLID
PRODUCT
LINES
Cell culture
Biocatalyst Bioreactor
Recovery
product
Feedstock Bioprocessing
Gas
− Syn. Gas
− CO2
− Organic vapor
Liquid
− Organic
− Sugar solution
Solid
− Biomass
− Consumer Waste
Immobilized Enzymes
− Ambient to Extreme
Fermentation
− Immobilized
− Free cell
− Ambient to Extreme
Bioreactors
− Continuous Systems
− Membrane
− Batch or Fed-batch
Separation
− In situ
− Secondary
Media
− Gaseous
− Aqueous
− Organic
Pharmaceuticals
Fine chemicals
Specialty Chemicals
Feedstock
Bulk chemicals
General
Bioprocess
Product
Link : https://www.youtube.com/watch?v=5eKdZ0dVCCo
19. Objectives
• Define microbial growth
• Distinguish between binary fission and budding
• Classify microbes into five groups on the basis of preferred temperature range
• Explain microbial growth at low and high pH
• Provide a use for each of the four elements (C, N, S, P) needed in large amounts
for microbial growth
• Distinguish between chemically defined and complex media
• Justify the use of each of the following: anaerobic techniques, living host cells,
candle jars, selective, differential, and enrichment media
• Review some direct and indirect methods of measuring bacterial cell growth
Microbial Growth
20. Definition
• Microbial Growth Defined:
1. Mother or parent cell doubles
in size
2. Divides into two daughter cells
• Microbial growth is defined as
the increase in the number of
cells, which occurs by cell
division
21. Thin section of the bacterium Staphylococcus,
undergoing binary fission
Budding
22. Bacterial Growth Curve
Illustrates the dynamics of growth
Phases of growth
•Lag phase
•Exponential or logarithmic (log)
phase
•Stationary phase
•Death phase (decline phase)
Compare growth in liquid and on solid media
23. Microbial growth: Increase in cell number, not cell size!
Physical Requirements for Growth: Temperature (cardinal temperature)
• Minimum growth temperature
• Optimum growth temperature
• Maximum growth temperature
Five groups based on optimum growth temperature
1. Psychrophiles
2. Psychrotrophs
3. Mesophiles
4. Thermophiles
5. Hyperthermophiles
Microbial Growth
Fig. 6 .3
24. Physical Requirements for Growth:
pH and Osmotic Pressure
Most bacteria grow best between pH 6.5 and 7.5: Neutrophils
Some bacteria are very tolerant of acidity or thrive in it: Acidophiles
(preferred pH range 1 to 5)
Alkaliphiles grow between pH range 9 to 11
Molds and yeasts grow best between pH 5 and 6
Hypertonic environments (increased salt or sugar) cause plasmolysis
Obligate halophiles vs.
facultative halophiles
26. Chemical Requirements for Growth: Oxygen
O2 requirements vary greatly
Table 6.1: The Effects of Oxygen on the Growth of Various Types of Bacteria
27. Chemical Requirements for Growth: Carbon, N,
S, P, etc.
• Carbon
• Half of dry weight
• Chemoheterotrophs use organic carbon sources
• Nitrogen, Sulfur, Phosphorus
• Needed for ?
• Found in amino acids and proteins
• S in thiamine and biotin
• Phosphate ions (PO4
3–)
(most bacteria decompose proteins)
• Also needed K, Mg, Ca, trace elements (as
cofactors), and organic growth factors
Vit B7
Vit B1
28. Culture Media
• Culture medium: Nutrients prepared for microbial growth
• Have to be sterile (not contain living microbes)
• Inoculum: Microbes introduced into medium
• Culture: Microbes growing in/on culture medium
• Chemically defined media: Exact chemical composition is known (for research purposes
only)
• Complex media: Extracts and digests of yeasts, meat, or plants, e.g.:
• Nutrient broth
• Nutrient agar
• Blood agar
29. Types of Culture Media
• Natural Media: In nature, many species of
microorganisms grow together in oceans, lakes, and soil
and on living or dead organic matter
• Synthetic medium: A medium prepared in the
laboratory from material of precise or reasonably
well-defined composition
• Complex medium: contains reasonably familiar material
but varies slightly in chemical composition from batch to
batch (e.g. peptone, a product of enzyme digestion of
proteins)
Commonly Used Media
• Yeast Extract
• Casein Hydrolysate
• Serum
• Blood agar
• Chocolate agar
30. Agar
•Complex polysaccharide
•Used as solidifying agent for culture media in
Petri plates, slants, and deeps
•Generally not metabo- lized by
microbes
•Liquefies at 100°C
•Solidifies ~40°C
31. The Growth of Bacterial Cultures
Binary fission – exponential growth
Budding
Generation time – time required for cell to divide (also
known as doubling time)
Ranges from 20 min (E. coli) to > 24h (M. tuberculosis)
Consider reproductive potential of E. coli
32. Serial Dilution and Standard Plate Counts
•Standard plate count: One method of
measuring bacterial growth
•Agar plate: A petri dish containing a
nutrient medium solidified with agar
•Serial dilutions are used to dilute the
original bacterial culture before you
transfer known volume of culture onto
agar plate
33. • Pour plate: made by first adding
1.0ml of diluted culture to 9ml of
molten agar
• Spread plate: made by adding
0.1ml of diluted culture to
surface of solid medium
Calculation of the number of
bacteria per milliliter of culture
using serial dilution
35. Direct Measurements of Microbial Growth
Viable cell counts: Plate counts: Serial dilutions
put on plates CFUs form colonies
36. Additional Direct Measurements
1. Filtration method of choice for low
counts
2. Direct microscopic count: Counting
chambers (slides) for microscope
38. CONCLUSION
1. (Muhammad Faiz)
- bacteria have 4 growth phase (log, exponent,
stationary, and death)
2. (Anastasia)
- Bioprocess is application of two department, ie
Microbiology and Chemical Engineering
- Bioprocess have 4 step : identification,
stoichiometry, kinetics, and design.
39. Next week :
Objective:
1. The control of microbial growth
2. The effect of microbial control agents on cellular
structures
3. Compare effectiveness of moist heat vs dry heat
4. Kinetics of microbial growth
Teknik Kimia Umum mudahnya mempelajari pemrosesan bahan baku menjadi barang jadi dengan menggunakan katalis konvensional (bahan kimia) sedangkan Teknik Bioproses mempelajari pemrosesan bahan baku menjadi barang jadi dengan menggunakan katalis mikrobiologi.
Dalam teknik kimia, fokus kajian yang dipelajari adalah industri proses berbasis katalis kimia. Dalam teknik bioproses, katalis yang digunakan adalah katalis biologis yang meliputi enzim, mikroba (bakteri dan jamur), serta sel tingkat tinggi (ini umumnya dipelajari di jurusan dengan rumpun keilmuan biologi).
Contoh penerapan ilmu Teknik Bioproses dalam industri misalnya industri bioetanol dari molasse. Apa agen biologis yang digunakan? Saccharomyces cerevisiae a.k.a ragi. Prosesnya? Fermentasi. Cara desain bioreaktor yang sesuai dengan kondisi lingkungan yang diinginkan mikroba sangat penting untuk dihighlight. Apakah prosesnya endoterm atau eksoterm. Bagaimana mempertahankan suhu di dalam bioreaktor/heat transfer. Apakah perlu menggunakan jacket atau tidak. Bagaimana teknik scale up dari skala lab, pilot hingga industri. Sistem gas buang untuk pengeluaran CO2 dari bioreaktor bagaimana. Teknik purifikasi produk bagaimana. Kenapa menggunakan teknik tersebut. Berapa persen kemurnian yang dihasilkan jika menggunakan teknik tersebut. Kalau pakai teknik lain, berapa persen kemurniannya. Apa limbah yang dihasilkan? Bagaimana teknik pengolahan limbah biar tidak mencemari lingkungan?