EC1105A - Group1 - ENUMERATION OF BACTERIA
EC1105A - Group1 - ENUMERATION OF BACTERIA
Laboratory
LEVEL 2 Team Student’s ID Student’s Name Group
Level
Laboratory Title ENUMERATION OF BACTERIA 1. Group Leader 2019400128 AHMAD MUHAIMIN BIN MUHAMMAD NASRAN EC110 5A - G1
Date 11 / 1 / 2022 2. Member 2019448406 AFIF IZZUDDIN BIN NOOR ILHAM EC110 5A - G1
Lecturer’s
Name
NOOR SAFWAN BIN MUHAMAD 3. Member 2019258558 MUHAMMAD FAIZ BIN ISMAIL EC110 5A - G1
4. Member
Verification
Demonstrate capability on the Demonstrate capability on the Demonstrate capability on the Demonstrate capability on the Demonstrate capability on the
following in a problem-solving following in a problem-solving following in a problem-solving following in a problem-solving following in a problem-solving
A4 (Organizing) approach as shown in lab approach as shown in lab approach as shown in lab approach as shown in lab report approach as shown in lab report
Brings together different report report report 75% organize, formatted 100% fully organize,
values, resolving conflicts Not organize, 25% organize, formatted 50% organize, formatted and systematic laboratory formatted and systematic
among them, and starting to unformatted and and systematic and systematic report laboratory report
build an internally consistent unsystematic laboratory laboratory report laboratory report 75% providing solution to 100% providing solution to
5 value system. Organizes Discussion report 25% providing solution 50% providing solution the environmental the environmental
values into priorities by Not providing solution to to the environmental to the environmental engineering problems. engineering problems.
contrasting different the environmental engineering problems. engineering problems. The team is able to relate The team is able to relate all
systems. The emphasis is on engineering problems. The team is able to The team is able to all findings with the findings with the problem
comparing, relating, and The team is unable to discuss some of the relate some of the problem with good with excellent discussion
synthesizing values. discuss the findings findings findings with the discussion
problem with fair
discussion
The team is able to provide The team is able to derive fair The team is able to derive good The team is able to derive accurate
6 A5 (Characterization) Conclusion The team is unable to conclude conclusion without answering conclusion based on findings to conclusion based on findings to conclusion based on findings to
the objective answer the objective answer the objective answer the objective
TOTAL
60
PROCEDURE
1. Ready a liquid sample for the experiment. This group (Group 1) using urine as liquid
sample.
2. The liquid sample divided into 3 conditions to put into a bottle. Pure urine liquid used
for first bottle. Second bottle, distilled water added into the liquid using pipet to be
diluted to 1:200. Third bottle, the liquid diluted to 1:1000.
3. 1 ml of liquid inside each bottle are taken using dropper and poured into membrane
filter plate separately for each bottle.
4. The plates are placed inside incubator for 36 hours with temperature of 35˚C.
5. The plates taken out and observed the presence of bacteria. Number of colonies are
counted and recorded.
DATA ANALYSIS
Result from the experiment obtained, 2 out of 3 samples shows the presence of bacteria
while the other is not.
From observation of the samples, there are no sign of bacteria colony or colour
changing in sample 1. Pure urine should not have presence of any bacteria besides coliform, so
the condition of this individual is healthy.
Sample 2 does show a sign of bacteria colony about 13 of average coliforms colony and
no e-coli detected after the dilution. The purpose of dilution is to get the bacteria into colony.
The lower ratio of dilution, the higher the size of bacteria colony. Pipet was used during this
process to ensure the exact amount volume of distilled water used. Observation on the sample
is quite blurry because the colour was blend in with the membrane filter brings difficulty to get
the exact amount of colony.
Sample 3 shows a lot of bacteria presence with the random numbers of coliform spots
and the change of colour are highly visible, pink colour to be exact. The number of colonies is
too much and too small to be counted, later it was decided to be uncountable. The dilution
should have made the bacteria to form large colony where it is opposite on this sample.
All data from the samples are recorded then calculated using the formula,
𝑇𝑜𝑡𝑎𝑙 𝑐𝑜𝑙𝑖𝑓𝑜𝑟𝑚 = (𝐶𝑜𝑙𝑖𝑓𝑜𝑟𝑚 + 𝐸𝑐𝑜𝑙𝑖) × 100 × 𝐷𝑖𝑙𝑢𝑡𝑖𝑜𝑛 𝐹𝑎𝑐𝑡𝑜𝑟. The best result of the
experiment is the Sample 2 in case of able to get exact amount of bacteria colony. Comparison
between the samples and National Drinking Water Standard, coliform must not be detected in
any 100 ml sample, which is Sample 1 is the safest but need to consider the colour and further
treatment.
CONCLUSION
The objectives of this experiment to quantify the presence of E-coli in liquid sample
and to compare result of experiment with National Drinking Water Standard was succeed.
Although, using urine as sample for this experiment is difficult to get satisfying result rather
than other sample such as cat’s dung, drain water or lake water. These samples are more likely
to have e-coli inside. For future experiment, dilution process is need to be focused because it
one of the factor of result failure.
APPENDICES
Figure 3&4: Samples from other group (Cat’s dung & River water).
REFERENCES