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Bacteriological 
measurement and its physical 
characteristics 
Presented by : 
satabdy Jena 
t14ee003 
Mtech 
Power and energy systeMs 
nIt Meghalaya
Contents 
2
Introduction 
3
Binary fission 
4
Fig1.Binary fission 
5
• Baeocyte production in the 
cyanobacterium Stanieria 
• It starts out as a small, spherical cell approximately 1 
to 2 μm in diameter. This cell is referred to as a 
baeocyte (which literally means "small cell"). The 
baeocyte begins to grow, eventually forming a 
vegetative cell up to 30 μm in diameter. As it grows, 
the cellular DNA is replicated over and over, and the 
cell produces a thick extracellular matrix. The 
vegetative cell eventually transitions into a 
reproductive phase where it undergoes a rapid 
succession of cytoplasmic fissions to produce dozens 
or even hundreds of baeocytes. The extracellular 
matrix eventually tears open, releasing the 
baeocytes. Other members of the Pleurocapsales (an 
Order of Cyanobacteria) use unusual patterns of 
division in their reproduction . 
6
7 
Fig 2. Baeocyte production
• Budding in bacteria 
• Budding has been observed in some members of 
the Planctomycetes, Cyanobacteria, Firmicutes 
(a.k.a. the Low G+C Gram-Positive Bacteria) and 
the prosthecate Proteobacteria. Although 
budding has been extensively studied in the 
eukaryotic yeast Saccharomyces cerevisiae, the 
molecular mechanisms of bud formation in 
bacteria are not known. 
8
9 
Fig 3.Budding
• Intracellular offspring production by 
some Firmicutes 
• Epulopiscium spp., Metabacterium 
polyspora and the Segmented Filamentous 
Bacteria (SFB) form multiple intracellular 
offspring. For some of these bacteria, this 
process appears to be the only way to 
reproduce. Intracellular offspring development 
in these bacteria shares characteristics with 
endospore formation in Bacillus subtilis. 
10
11 
Fig 4.Intracellular offspring production
12
• Four characteristic phases of the growth 
cycle are recognized as : 
• Lag phase 
• Exponential(log) phase 
• Stationary phase 
• Death phase 
13
14 
Fig 5.Bacterial growth curve
15
• Methods for Measurement of Cell Mass 
• Methods for measurement of the cell mass involve both direct and 
indirect techniques. 
1. Direct physical measurement of dry weight, wet weight, or volume of 
cells after centrifugation. 
2. Direct chemical measurement of some chemical component of the cells 
such as total N, total protein, or total DNA content. 
3. Indirect measurement of chemical activity such as rate of O2 production 
or consumption, CO2 production or consumption, etc. 
4. Turbidity measurements employ a variety of instruments to determine 
the amount of light scattered by a suspension of cells. Particulate objects 
such as bacteria scatter light in proportion to their numbers. The turbidity 
or optical density of a suspension of cells is directly related to cell mass or 
cell number, after construction and calibration of a standard curve. The 
method is simple and nondestructive, but the sensitivity is limited to about 
107 cells per ml for most bacteria. 
16
17 
Fig 6. Filtration
18 
Fig 7.Turbidity measurement
• Methods for Measurement of Cell Numbers 
• 1. Direct microscopic counts are possible using 
special slides known as counting chambers. Dead 
cells cannot be distinguished from living ones. Only 
dense suspensions can be counted (>107 cells per 
ml), but samples can be concentrated by 
centrifugation or filtration to increase sensitivity. 
• A variation of the direct microscopic count has been 
used to observe and measure growth of bacteria in 
natural environments. In order to detect and prove 
that thermophilic bacteria were growing in boiling 
hot springs, T.D. Brock immersed microscope slides 
in the springs and withdrew them periodically for 
microscopic observation. The bacteria in the boiling 
water attached to the glass slides naturally and grew 
as microcolonies on the surface. 
19
20
21 
Fig 8. Direct measurement of microbial growth
22 
Fig 9.Plate method
23
24
25
• [1]Physical factors affecting microbial growth, 
Wikipedia 
• [2]The growth of bacterial population, Kenneth 
Todar 
• [3]Theory and measurement of bacterial growth, 
Fredrich Widdel, Universitat Bremen 
• [4]The growth of bacterial cultures 
• [5] Factors Affecting Bacterial Growth, Shayna 
Goodman 
26
27

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Bacteriological measurement and its physical characteristics

  • 1. Bacteriological measurement and its physical characteristics Presented by : satabdy Jena t14ee003 Mtech Power and energy systeMs nIt Meghalaya
  • 6. • Baeocyte production in the cyanobacterium Stanieria • It starts out as a small, spherical cell approximately 1 to 2 μm in diameter. This cell is referred to as a baeocyte (which literally means "small cell"). The baeocyte begins to grow, eventually forming a vegetative cell up to 30 μm in diameter. As it grows, the cellular DNA is replicated over and over, and the cell produces a thick extracellular matrix. The vegetative cell eventually transitions into a reproductive phase where it undergoes a rapid succession of cytoplasmic fissions to produce dozens or even hundreds of baeocytes. The extracellular matrix eventually tears open, releasing the baeocytes. Other members of the Pleurocapsales (an Order of Cyanobacteria) use unusual patterns of division in their reproduction . 6
  • 7. 7 Fig 2. Baeocyte production
  • 8. • Budding in bacteria • Budding has been observed in some members of the Planctomycetes, Cyanobacteria, Firmicutes (a.k.a. the Low G+C Gram-Positive Bacteria) and the prosthecate Proteobacteria. Although budding has been extensively studied in the eukaryotic yeast Saccharomyces cerevisiae, the molecular mechanisms of bud formation in bacteria are not known. 8
  • 10. • Intracellular offspring production by some Firmicutes • Epulopiscium spp., Metabacterium polyspora and the Segmented Filamentous Bacteria (SFB) form multiple intracellular offspring. For some of these bacteria, this process appears to be the only way to reproduce. Intracellular offspring development in these bacteria shares characteristics with endospore formation in Bacillus subtilis. 10
  • 11. 11 Fig 4.Intracellular offspring production
  • 12. 12
  • 13. • Four characteristic phases of the growth cycle are recognized as : • Lag phase • Exponential(log) phase • Stationary phase • Death phase 13
  • 14. 14 Fig 5.Bacterial growth curve
  • 15. 15
  • 16. • Methods for Measurement of Cell Mass • Methods for measurement of the cell mass involve both direct and indirect techniques. 1. Direct physical measurement of dry weight, wet weight, or volume of cells after centrifugation. 2. Direct chemical measurement of some chemical component of the cells such as total N, total protein, or total DNA content. 3. Indirect measurement of chemical activity such as rate of O2 production or consumption, CO2 production or consumption, etc. 4. Turbidity measurements employ a variety of instruments to determine the amount of light scattered by a suspension of cells. Particulate objects such as bacteria scatter light in proportion to their numbers. The turbidity or optical density of a suspension of cells is directly related to cell mass or cell number, after construction and calibration of a standard curve. The method is simple and nondestructive, but the sensitivity is limited to about 107 cells per ml for most bacteria. 16
  • 17. 17 Fig 6. Filtration
  • 18. 18 Fig 7.Turbidity measurement
  • 19. • Methods for Measurement of Cell Numbers • 1. Direct microscopic counts are possible using special slides known as counting chambers. Dead cells cannot be distinguished from living ones. Only dense suspensions can be counted (>107 cells per ml), but samples can be concentrated by centrifugation or filtration to increase sensitivity. • A variation of the direct microscopic count has been used to observe and measure growth of bacteria in natural environments. In order to detect and prove that thermophilic bacteria were growing in boiling hot springs, T.D. Brock immersed microscope slides in the springs and withdrew them periodically for microscopic observation. The bacteria in the boiling water attached to the glass slides naturally and grew as microcolonies on the surface. 19
  • 20. 20
  • 21. 21 Fig 8. Direct measurement of microbial growth
  • 22. 22 Fig 9.Plate method
  • 23. 23
  • 24. 24
  • 25. 25
  • 26. • [1]Physical factors affecting microbial growth, Wikipedia • [2]The growth of bacterial population, Kenneth Todar • [3]Theory and measurement of bacterial growth, Fredrich Widdel, Universitat Bremen • [4]The growth of bacterial cultures • [5] Factors Affecting Bacterial Growth, Shayna Goodman 26
  • 27. 27