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Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2025
Isolation, Characterization, and Application of Calcite Producing
Bacteria for Self-Healing Concrete Preparation
Diksha H. Jokyani
1
, Dharmvir Chouhan
2
*
1
Student, P. G Department of Microbiology, Dhote Bandhu Science College, Gondia, India
2
Assistant Professor cum HOD, P. G Department of Microbiology, Dhote Bandhu Science College, Gondia, India
*Address for Correspondence: Prof. D. A. Chouhan, Assistant Professor cum HOD, P.G Department of Microbiology,
Dhote Bandhu Science College, Kudwa Road Gondia, Maharashtra- 441614, India
Received: 18 Apr 2018/ Revised: 05 Jun 2018/ Accepted: 02 Aug 2018
ABSTRACT
Concrete being the foremost building material broadly used in the construction sector is subjected to crack formation due to low
tensile strength, durability, and ductility. So this issue is of great curiosity to the researchers in pursuit for the concrete production
with better properties. Micro-cracks are the main reason for structural failure occurs, when the load applied exceeds its limits.
This causes the seepage of water and other salts. In order to overcome this, the carbonate precipitating, non-pathogenic, spore-
forming, alkaline resistant strain of Bacillus subtilis has been explored as a bio-cementing material. Cracks in M20 grade concrete
blocks are injected by direct means with screened bacterial strain Bacillus subtilis (BH3) at the cell concentration of 10
4
, 10
5
, 10
6
CFU/ml with silica gel as an immobilizing agent and calcium lactate as a food source. The cracks were allowed to heal for
appropriate time duration at specific pH, temperature, and urea concentration. These findings suggest the potential of Bacillus
subtilis in an autogenously healing process.
Key-words: Bacillus subtilis, BH3, Carbonate precipitation, Calcite, Self healing and Bio-cementation
INTRODUCTION
A large amount of non-renewable resource is consumed
by the construction engineering sector, most of which
contribute to the highest proportion of global CO2
emission at their production or application stage. The
concrete production process is an energy-intensive
process if in case of mining, transportation and
processing are considered. Its production level lies at
about 2.35 billion metric tonnes per year and contributes
an astonishing 10% of CO2 emission in the atmosphere [1]
.
Another issue concerns is the huge maintenance costs
for structure built in past. About 10% of the bridges in
the USA are considered structurally deficient and 10% of
it is considered functionally obsolete [2]
. Apart from this
the factors like freeze-thaw reactions, shrinkage, results
How to cite this article
Jokyani DH, Chouhan D. Isolation, Characterization, and
Application of Calcite Producing Bacteria for Self-Healing Concrete
Preparation. Int. J. Life. Sci. Scienti. Res., 2018; 4(5): 2025-2036.
Access this article online
www.ijlssr.com
in the cracking of concrete structures during its
hardening and this ultimately leads to structural
deformation. Latter the ingress of some hazardous
chemicals and moisture into the concrete may lead to
decrement in its serviceability whereas; the penetration
of sulphates and chlorides in cracks causes the durability
to be affected. Hence the more concern should be given
to this so as to prevent the expansion of cracks by a
sustainable means that might involve the natural
microbial mechanism of bio-cementation which is
promising.
Autonomously healed concrete is nothing but the
biologically produced limestone by which the cracks can
be healed effectively. The screened bacterial strain of
genus โ€œBacillusโ€ along with the calcium based nutrient
like calcium lactate and an immobilizing agent like silica
gel is mixed in appropriate proportion and injected into
the preformed cracks by direct means. In case if it is
added initially to the concrete mixture then the
self-healing agent can lie in the dormant stage within the
concrete for up to about 200 years. Due to any of the
damage the water starts to percolate deep into the
structure and the dormant bacterial form if get the
Research Article
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2026
growth favourable conditions to acquire its vegetative
form and starts to feed on calcium lactate consuming
oxygen and thereby converting soluble calcium lactate to
insoluble calcium carbonate better called limestone.
Here the consumption of oxygen by the bacterial strain is
advantageous as oxygen is responsible for steel
corrosion thereby enhancing the durability of steel
structures [3]
, Since 1980โ€™s several researchers had been
working on this concept and had used the different
bacterial strains such as Jonker et al. [4]
used Bacillus
cohnii bacteria to precipitate CaCO3 while Santhosh et al.
[5]
and Bang et al. [6]
used Bacillus pasteurii.
As the bacterial cell wall is negatively charged, it will
draw the cations from the environment, Ca2+
and deposit
it on their cell surface serving as a nucleation site [6]
.
Ca2+
+ Cell Cell-Ca2+
1
This bacterial genus is known to have specific urease
activity that is utilized for the hydrolysis of urea into 1
mole of ammonia and 1 mole of carbonic acid [7]
.
H2N-CO-NH2 + H2O NH3 + H2N-CO-OH 2
H2N-CO-OH + H2O NH3 + H2CO3 3
These two products was subsequently form 2 moles of
ammonium and hydroxide ion as,
H2CO3 HCO3-
+ H+
4
2NH3 + 2H2O 2NH4
+
+ 2OH-
5
Reaction 4 and 5 turned in results in pH increase and
shifts the equilibrium, resulting in the carbonate ion
formation as,
HCO3-
+ H+
+2NH4
+
+2OH-
CO3
2-
+2NH4
+
+ 2H2O 6
The carbonate formed in reaction 6 was subsequently
reacted with Ca2+
ions deposited on bacterial cell wall,
leading to CaCO3 precipitation.
Cell-Ca2+
+ CO3
2-
Cell- CaCO3 7
MATERIALS AND METHODS
Materials and Chemical used- Soil samples used for
isolation of potent strain were collected from 12
different construction sites across the Gondia district,
India. All the required chemicals in this work were
purchased from Hi-media laboratories, India. The
research work was carried out in the P.G Department of
Microbiology, Dhote Bandhu Science College, Gondia,
India from August 2017 to March 2018.
Preparation and artificial cracking of concrete blocks-
The concrete blocks of M20 grade were first prepared
with the mould size of 100 mm x 60 mm and left for 28
days curing process. Further, the blocks were subjected
to indigenous cracking by plastic shrinkage method
(plastic shrinkage cracks usually ranges between 1-2 mm
depth) [8]
.
Determining Size of cracks- Size of the cracks in concrete
block was measured using scale [9]
.
Isolation of new ureolytic bacteria- Soil samples
pasteurized at 800
C for 15 minutes then subjected to
tenfold dilution. The 0.2 ml of pasteurized diluted sample
was then plated on sterile urea agar plates with 5% urea
concentration. Plates were incubated at 370
C for 24 - 48
hrs and observed the isolated colonies. Pink color
colonies were selected and further screened based on
the capability to degrade urea in Christensenโ€™s agar
medium and to tolerate high alkaline condition based on
pH optimization studies. The single selected potent
organism was in turn identified based on its
morphological and biochemical characteristics. Latter on
the identified isolate was pure cultured on urea agar
slants and preserved at low temperature (40
C) [10]
.
Study on effect of environmental and nutritional
condition on urease production a capability of BH3
strains- Bacillus subtilis strain with promising result was
selected and the effect of environmental condition like
temperature, and nutritional condition such as urea
concentration were characterized. For temperature
optimization, 1 ml of overnight growth culture was
inoculated in 3 tubes containing urease broth except the
control tube and incubated at 3 different temperature
ranges as 250
C, 350
C, and 450
C then after 24 hours the
tubes were observed for change in color intensity and
biomass was determined nephlometrically. For urea
concentration, optimization purpose 1 ml of overnight
growth culture was inoculated in 3 tubes containing urea
in concentration range of 2%, 5%, and 10% except the
control tube and incubated at 350
C. After 24 hours the
tubes were observed for change in color intensity and
biomass was determined nephlometrically. [11]
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2027
Growth Curve of Bacillus subtilis strains: The growth
curve of screened isolate was determined to set a
growth comparison point at optimum condition. Three
ml of overnight growth culture was used to inoculate in
30 ml of urea broth in 250 ml conical flask then the
culture was incubated for 27 hours at 350
C, pH 8, and 5%
urea concentration. Inoculation time was considered as
zero time and the quantitative determination of growth
was carried out by spectrophotometer at 600 nm.
Simultaneously the viable cell count was determined as a
colony forming units/ml (CFUs) [12]
. The desired isolate
was purified and mixed with silica gel in 1: 100 dilution
factors with the cell count 104
, 105
, 106
cells so as to
immobilize the bacterial cells and hence it can remain
embedded for the long time in the concrete matrix.
Along with it, calcium lactate is also added to it with
molar mass 218 g/mole that serve as food source for
bacterial cells. As it gets the growth favorable conditions
it will soon start to precipitate CaCO3 and the bacterial
cells will be in turn coated with it resulting in the
autogenous healing [13]
.
Water Permeability Test of Concrete- To determine the
water absorption ability of bacterial concrete, this test
was carried out in a comparative manner. For this, the
control and bacteria treated concrete blocks were kept
overnight saturated in the saline buffer and weighed.
Then both blocks were dried in the oven at 1000
C for 24
hours, cooled and again weighed. The obtained values
were then put into the formula given below to
determine percent water absorption by both the
blocks [14]
.
WSaturation โ€“ WOven Dried
% water absorption =
WOven Dried
Where,
WSaturation = Weight of block after saturation
WOven Dried= Weight of block after drying
RESULTS
As the durability of concrete is affected by the cracks
leading to corrosion of reinforcing bars, the general
method of repairing is time consuming and expensive, so
bio based calcite precipitation has been proposed as an
alternative and sustainable, environment friendly cracks
repair technique. The bio agent selected for this purpose
was based on its tolerance to high pH, and continuous
formation of dense CaCO3 in the liquid medium.
According to analysis and study of blocks by the visual
examination of concrete core, the estimated size of
cracks varied from 0.3 to 0.5 mm [9]
. Total 12 urease
positive Bacillus subtilis strains were isolated from soil
sample. Out of these 12 isolates Bacillus subtilis BH3
strains were found to be most potent.
Optimization- The optimum temperature required for
growth of Bacillus subtilis was 350
C. Table 1 and Fig. 1
shows the optimization of temperature by using 3
different temperature ranges.
Table 1: Measurement of bacterial growth at 3 different temperature ranges
S. No. Bacterial strains
Temperature range
(0
C)
Growth measure
Ureolytic activity Interpretation
OD600
1.
BH3
25 1.51
Color changes to
mild pink
The maximum
ureolytic activity
with effective
growth was
observed at
temperature range
of 350
C
2. 35 1.52
Color changes to
intense pink
3. 45 1.519
Color changes to
light pink
BH3= Bacillus subtilis
The specific urea concentration supporting the growth
of selected ureolytic bacterial strains (BH3) was 5%. The
Table 2 and Fig. 2 show the effect of urea concentration
on the bacterial growth and urea degrading ability of it.
X 100
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2028
1.505
1.51
1.515
1.52
1.525
25 35 45
Absorbanceat600nm
Temperature range (0C)
Effectof Temperature on growth of BH3
strain
Fig. 1: Effect of temperature on growth of Bacillus subtilis strains
Table 2: Measurement of bacterial growth at 3 different urea concentrations
0
0.5
1
1.5
2
2% 5% 10%
Absorbanceat600nm
Urea concentration
Effect of urea concentration on growth of BH3
strain
Fig. 2: Effect of urea concentration on growth rate of Bacillus subtilis strains
Spectroscopic growth curve- The growth curve of
Bacillus subtilis was elucidated using the partially
optimized condition. Table 3 and Fig. 3 indicate the
growth curve of B. subtilis isolates, which is considered
as the selected isolate of this research paper.
The maximum OD was seen between 6 to 10 hours and
referred as log phase. Nephlometric reading showed that
the cultures reached the stationary phase after 10 hours.
After 24 hours the bacterial growth was inhibited due to
media component depletion and the release of
secondary metabolite that may be toxic to viable cells.
S. No.
Bacterial
strains
Urea
concentration
Growth measure
Ureolytic activity Interpretation
OD600
1.
BH3
2% 0.54 Color changes to light pink The maximum
ureolytic activity
with effective
growth was
observed at 5% urea
concentration
2. 5% 1.75
Color changes to Intense
pink
3. 10% 1.69 Color changes to mild pink
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2029
Table 3: Nephlometric absorbance values to construct growth curve of screened isolate of B. subtilis
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
1.8
2
1 2 3 4 6 8 9 10 11 12 25 26 27
ODat600nm
Hours of incubation
Growth curve of strain BH3
Fig. 3: Growth curve of screened potent isolate of B. subtilis strains
Studies on concrete crack healing potential of BH3
strains- In this investigation, the 3 concrete blocks, Block
1, Block 2, and Block 3 were used for autogenous healing
by the selected strains of Bacillus subtilis. Block 1 with
crack size of 0.45 mm width was injected with 105
CFU/
ml along with silica gel and calcium lactate showed the
healing of cracks at 21st
day of inoculation and the width
of crack was reduced to 0.18 mm.
Similarly the Block 2 with crack size of 0.52 mm when
injected with 106
CFU/ml showed the efficient healing on
19th
day of inoculation, whereas the Block 3 with crack
size 0.48 mm width, when injected with 104
CFU/ml,
showed the healing on 23rd
day of inoculation with the
reduction in crack size up to 0.25 mm.
Absorbance at 600 nm
Time in hours Trial 1 Trial 2 Trial 3 Average
1 0.162 0.164 0.180 0.168
2 0.372 0.343 0.417 0.377
3 0.651 0.621 0.682 0.651
4 0.911 1.001 1.073 0.995
6 1.400 1.545 1.521 1.488
8 1.618 1.647 1.690 1.651
9 1.671 1.677 1.700 1.682
10 1.720 1.677 1.710 1.702
11 1.723 1.694 1.721 1.712
12 1.731 1.717 1.729 1.725
25 1.019 1.724 0.940 1.227
26 0.911 0.853 0.848 0.870
27 0.908 0.847 0.769 0.841
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2030
Table 4: Concrete crack healing potential of B. subtilis strains in block 1 (105
cells/ml)
S. No. Date Initial Characteristics Final characteristic (Width) Interpretation
1. 22nd
January
Grade: M20
Size: 100 X 60 mm
Curing: 28 days
Crack developed by:
plastic shrinkage type
Width: 0.45 mm
0.45 mm
Block 1, inoculated
with the 105
cells/ml
of BH 3 strains,
showed the
effective healing
within 21 days from
the day of
inoculation
2. 23rd
January 0.45mm
3. 24th
January 0.44 mm
4. 25th
January 0.43 mm
5. 26th
January 0.41 mm
6. 27th
January 0.4 mm
7. 28th
January 0.4 mm
8. 29th
January 0.38 mm
9. 30th
January 0.37 mm
10. 31st
January 0.37 mm
11. 1st
February 0.35mm
12. 2nd
February 0.34 mm
13. 3rd
February 0.31 mm
14. 4th
February 0.28 mm
15. 5th
February 0.27 mm
16. 6th
February 0.25 mm
17. 7th
February 0.23 mm
18 8th
February 0.2 mm
19. 9th
February 0.19 mm
20. 10th
February 0.19 mm
21. 11th
February 0.18 mm
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2031
Fig. 4: Crack healing study in bacteria treated cracked concrete block (Block 1)
Table 5: Concrete crack healing potential of B. subtilis strains in block 2 (106
cells/ml)
S. No. Date
Block characteristics Final characteristic
(Width)
Interpretation
1. 22nd
January
Grade: M20
Size: 100 X 60 mm
Curing: 28 days
Crack developed by:
plastic shrinkage type
Width: 0.52 mm
0.52 mm
Block 2, inoculated with the
106
cells/ml of BH 3 strains,
showed the effective healing
within 19 days from the day of
inoculation
2. 23rd
January 0.52 mm
3. 24th
January 0.52 mm
4. 25th
January 0.518mm
5. 26th
January 0.516 mm
6. 27th
January 0.514 mm
7. 28th
January 0.51 mm
8. 29th
January 0.48 mm
9. 30th
January 0.47 mm
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2032
10. 31st
January 0.47 mm
11. 1st
February 0.46 mm
12. 2nd
February 0.44 mm
13. 3rd
February 0.44 mm
14. 4th
February 0.4 mm
15. 5th
February 0.4 mm
16. 6th
February 0.4 mm
17. 7th
February 0.39 mm
18. 8th
February 0.39 mm
19. 9th
February 0.38 mm
Fig. 5: Crack healing study in bacteria treated cracked concrete block (Block 2)
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2033
Table 6: Concrete crack healing potential of B. subtilis strains in block 3 (104
cells/ml)
S. No. Date Block characteristics Final characteristic (Width) Interpretation
1. 22nd
January
Grade: M20
Size: 100 X 60 mm
Curing: 28 days
Crack developed by:
plastic shrinkage
type
Width: 0.48 mm
0.52 mm
Block 3, inoculated with the
104
cells/ml of BH3 strains,
showed the effective healing
within 23 days from the day
of inoculation
2. 23rd
January 0.52 mm
3. 24th
January 0.52 mm
4. 25th
January 0.518mm
5. 26th
January 0.516 mm
6. 27th
January 0.514 mm
7. 28th
January 0.51 mm
8. 29th
January 0.48 mm
9. 30th
January 0.47 mm
10. 31st
January 0.47 mm
11. 1st
February 0.46 mm
12. 2nd
February 0.44 mm
13. 3rd
February 0.44 mm
14. 4th
February 0.4 mm
15. 5th
February 0.4 mm
16. 6th
February 0.4 mm
17. 7th
February 0.39 mm
18. 8th
February 0.39 mm
19. 9th
February 0.38 mm
20. 10th
February 0.26 mm
21. 11th
February 0.26 mm
22. 12th
February 0.25 mm
23. 13th
February 0.25 mm
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2034
Fig. 6: Crack healing study in bacteria treated cracked concrete block (Block 3)
Water absorption test by using saline buffer- The saline
buffer is used in this research work so as to determine
the increased resistance of concrete block towards the
water penetration and this test was conducted at a
laboratory level. According to this test, the normal
concrete block had shown the higher water absorption
as compared to the concrete block treated with potent
ureolytic bacterial BH3 strains. Table 7 numerically
represents the bacterial influence on the water
permeability of blocks.
Table 7: Water saturation test results of bacteria healed cracked concrete
Blocks No. Weight (Saturation) Weight (Dried) Water absorption (%)
Block 1 192.73 183.70 4.91%
Block 2 188.05 174.80 7.58%
Block 3 152.30 140.10 8.70%
Control 131.1 119.4 9.79%
Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2035
DISCUSSION
This study has revealed the BH3 strains of bacterial
species (Bacillus subtilis) isolated from commercial
construction sites, have the high ureolytic activity and
can tolerate the pH range up to 12, which becomes the
primary factor for bio-cementation. Salmabanu L and
Suthar G [2]
stated this genus of endolithic bacteria can
resist the pH range up to 13 and persist for the long
duration with efficient ureolytic activity. The isolated and
screened potent isolate (BH3) was identified
phenotypically and biochemically same as done by Achal
et al. [11]
and Cheng et al. [15]
while the species level
characterization was achieved by 16s gene sequencing
technique. From the further optimization studies of BH3
strains, it was clear that it shows the effective urea
degrading activity at temperature 350
C with 5% urea
concentration. Similar conclusion was given by Steubing
[12]
, who stated that change in temperature and
nutritionally sound components can also affect the
CaCO3 precipitation efficiency by ureolytic bacteria.
Growth curve of this potent strains were determined
nephlometrically that showed the log phase of these
strains during initial 6-10 hours and become stationary
after 10 hours further reduction in the growth rate after
24 hours. The cell count in the range 105
CFU/ml when
injected in block 1 with the crack width size of 0.45 mm
shows the significant reduction in crack size up to 0.18 in
21 days after inoculation which was more effective as
compared to other 2 concrete block injected with 106
and 104
CFU/ml cells. A similar finding was reported by
Bai and Varghese [16]
during an experimental
investigation on the strength properties of fly ash based
bacterial concrete.
The bacteria treated concrete block shows the significant
reduction in its water penetration ability compared to
normal concrete block due to the deposition of CaCO3
matrix like structure around the bacterial cells thereby
blocking the pores and inhibiting the water percolation
through it. As with constant development in the field of
civil engineering and increasing CO2 emission,
considerable efforts has been devoted to this alternative
concept of bio healing of concrete.
CONCLUSIONS
Our paper describes that due to its self-healing abilities,
eco-friendly nature, resistance to water absorption
thereby enhancing the strength of building materials
along with prevention of steel corrosion, the microbial
concrete technology had proved to be better than the
conventional technologies. It may also be termed as
โ€œSmart Bio Materialโ€. The overall development of
strength in bio-concrete is attributed to significant
reduction in water absorption capability by using potent
bacterial strains of Bacillus subtilis immobilized by means
of silica gel and supplemented with calcium lactate as
food source. The efficient healing was shown with 105
cells, in block 1 with the reduction in crack size from 0.43
mm to 0.29 mm width at 21st
day of inoculation.
More exploratory works at large scale should be
undertaken to determine the efficacy of bio cementation
for consolidations of building. To make the process
economical, microbial additives can repaired by
industrial growth of cells by employing the products as
lactose mother liquor and corn step liquor as nutrient
source. Also, the durability of bacterial concrete should
be studied under the various weathering conditions.
ACKNOWLEDGMENTS
The author is grateful to P.G. Department of
Microbiology, Dhote Bandhu Science College, India for
their help and support in carrying out the present study.
Technical assistance and advice was provided by Dr. D. A.
Chouhan so I would like to thank him for his
encouragement.
CONTRIBUTION OF AUTHORS
Research concept- Prof. D. A. Chouhan
Research design- Prof. D. A. Chouhan
Supervision- Prof. D. A. Chouhan
Data collection- Diksha H. Jokyani
Data analysis and interpretation- Diksha H. Jokyani
Literature search- Diksha H. Jokyani
Writing article- Diksha H. Jokyani, Prof. D. A. Chouhan
Critical review- Prof. D. A. Chouhan
Article editing- Prof. D. A. Chouhan
Final approval- Prof. D. A. Chouhan
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Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716
Jokyani and Chouhan, 2018
DOI:10.21276/ijlssr.2018.4.5.10
Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2036
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2001; 287(4): 404-409.
[7] Reinhardt HW, Joo M. Permeability and self-healing
of cracked concrete as a function of temperature and
crack width. Cement and Concrete Research, 2003;
33: 981-985.
[8] Dick J, De. Windt W, De Graef B, Saveyn H, Vander
Meeren P, De Belie N, Verstraete W. Bio-deposition
of a calcium carbonate layer on degraded limestone
by Bacillus species, Biodegradation, 2006; 17(4):
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[9] Shetty MS. Concrete Technology theory and practice.
Revised ed., India; Schand publication: 2006; p. 361-
362.
[10]Sahmaran M, Keskin SB, Ozerkan G, Yaman IO. Self
healing of mechanically-loaded self consolidating
concretes with high volumes of fly ash. Cement and
Concrete Composites, 2008; 30(10): 872-879.
[11]Achal V, Mukherjee A, Reddy S. Characterization of
two urease-producing and calcifying Bacillus spp.
isolated from cement. J. Microbiol. Biotechnol, 2010;
20(11): 1571โ€“1576.
[12]Steubing P. Isolation of an Unknown Bacterium from
Soil. Proceedings of the 14th
Workshop/Conference
of the Association for Biology Laboratory Education
(ABLE), 1993; p. 240.
[13]Kantha DA, Sathyanarayanan KS, Darshan BS, Raja
RB. Studies on the characterization of Biosealant
properties of Bacillus sphaericus. International
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[14]Irwan JM, Faisal Alshalif A, Othman N, Anneza LH.
Effect of Ureolytic Bacteria on Compressive strength
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International Conference on Civil, Architectural,
Structural and Construction Engineering, 2015.
[15]Cheng L, Cord-Ruwisch R. In situ soil cementation
with ureolytic bacteria by surface percolation.
Ecological Engineering, 2012; 42: 64-72.
[16]Bai CP, Varghese S. An experimental investigation on
the strength properties of fly ash based bacterial
concrete. International Journal of Innovative
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64-69.
Open Access Policy:
Authors/Contributors are responsible for originality, contents, correct references, and ethical issues. IJLSSR publishes all articles under Creative
Commons Attribution- Non-Commercial 4.0 International License (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/legalcode

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Isolation, Characterization, and Application of Calcite Producing Bacteria for Self-Healing Concrete Preparation

  • 1. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2025 Isolation, Characterization, and Application of Calcite Producing Bacteria for Self-Healing Concrete Preparation Diksha H. Jokyani 1 , Dharmvir Chouhan 2 * 1 Student, P. G Department of Microbiology, Dhote Bandhu Science College, Gondia, India 2 Assistant Professor cum HOD, P. G Department of Microbiology, Dhote Bandhu Science College, Gondia, India *Address for Correspondence: Prof. D. A. Chouhan, Assistant Professor cum HOD, P.G Department of Microbiology, Dhote Bandhu Science College, Kudwa Road Gondia, Maharashtra- 441614, India Received: 18 Apr 2018/ Revised: 05 Jun 2018/ Accepted: 02 Aug 2018 ABSTRACT Concrete being the foremost building material broadly used in the construction sector is subjected to crack formation due to low tensile strength, durability, and ductility. So this issue is of great curiosity to the researchers in pursuit for the concrete production with better properties. Micro-cracks are the main reason for structural failure occurs, when the load applied exceeds its limits. This causes the seepage of water and other salts. In order to overcome this, the carbonate precipitating, non-pathogenic, spore- forming, alkaline resistant strain of Bacillus subtilis has been explored as a bio-cementing material. Cracks in M20 grade concrete blocks are injected by direct means with screened bacterial strain Bacillus subtilis (BH3) at the cell concentration of 10 4 , 10 5 , 10 6 CFU/ml with silica gel as an immobilizing agent and calcium lactate as a food source. The cracks were allowed to heal for appropriate time duration at specific pH, temperature, and urea concentration. These findings suggest the potential of Bacillus subtilis in an autogenously healing process. Key-words: Bacillus subtilis, BH3, Carbonate precipitation, Calcite, Self healing and Bio-cementation INTRODUCTION A large amount of non-renewable resource is consumed by the construction engineering sector, most of which contribute to the highest proportion of global CO2 emission at their production or application stage. The concrete production process is an energy-intensive process if in case of mining, transportation and processing are considered. Its production level lies at about 2.35 billion metric tonnes per year and contributes an astonishing 10% of CO2 emission in the atmosphere [1] . Another issue concerns is the huge maintenance costs for structure built in past. About 10% of the bridges in the USA are considered structurally deficient and 10% of it is considered functionally obsolete [2] . Apart from this the factors like freeze-thaw reactions, shrinkage, results How to cite this article Jokyani DH, Chouhan D. Isolation, Characterization, and Application of Calcite Producing Bacteria for Self-Healing Concrete Preparation. Int. J. Life. Sci. Scienti. Res., 2018; 4(5): 2025-2036. Access this article online www.ijlssr.com in the cracking of concrete structures during its hardening and this ultimately leads to structural deformation. Latter the ingress of some hazardous chemicals and moisture into the concrete may lead to decrement in its serviceability whereas; the penetration of sulphates and chlorides in cracks causes the durability to be affected. Hence the more concern should be given to this so as to prevent the expansion of cracks by a sustainable means that might involve the natural microbial mechanism of bio-cementation which is promising. Autonomously healed concrete is nothing but the biologically produced limestone by which the cracks can be healed effectively. The screened bacterial strain of genus โ€œBacillusโ€ along with the calcium based nutrient like calcium lactate and an immobilizing agent like silica gel is mixed in appropriate proportion and injected into the preformed cracks by direct means. In case if it is added initially to the concrete mixture then the self-healing agent can lie in the dormant stage within the concrete for up to about 200 years. Due to any of the damage the water starts to percolate deep into the structure and the dormant bacterial form if get the Research Article
  • 2. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2026 growth favourable conditions to acquire its vegetative form and starts to feed on calcium lactate consuming oxygen and thereby converting soluble calcium lactate to insoluble calcium carbonate better called limestone. Here the consumption of oxygen by the bacterial strain is advantageous as oxygen is responsible for steel corrosion thereby enhancing the durability of steel structures [3] , Since 1980โ€™s several researchers had been working on this concept and had used the different bacterial strains such as Jonker et al. [4] used Bacillus cohnii bacteria to precipitate CaCO3 while Santhosh et al. [5] and Bang et al. [6] used Bacillus pasteurii. As the bacterial cell wall is negatively charged, it will draw the cations from the environment, Ca2+ and deposit it on their cell surface serving as a nucleation site [6] . Ca2+ + Cell Cell-Ca2+ 1 This bacterial genus is known to have specific urease activity that is utilized for the hydrolysis of urea into 1 mole of ammonia and 1 mole of carbonic acid [7] . H2N-CO-NH2 + H2O NH3 + H2N-CO-OH 2 H2N-CO-OH + H2O NH3 + H2CO3 3 These two products was subsequently form 2 moles of ammonium and hydroxide ion as, H2CO3 HCO3- + H+ 4 2NH3 + 2H2O 2NH4 + + 2OH- 5 Reaction 4 and 5 turned in results in pH increase and shifts the equilibrium, resulting in the carbonate ion formation as, HCO3- + H+ +2NH4 + +2OH- CO3 2- +2NH4 + + 2H2O 6 The carbonate formed in reaction 6 was subsequently reacted with Ca2+ ions deposited on bacterial cell wall, leading to CaCO3 precipitation. Cell-Ca2+ + CO3 2- Cell- CaCO3 7 MATERIALS AND METHODS Materials and Chemical used- Soil samples used for isolation of potent strain were collected from 12 different construction sites across the Gondia district, India. All the required chemicals in this work were purchased from Hi-media laboratories, India. The research work was carried out in the P.G Department of Microbiology, Dhote Bandhu Science College, Gondia, India from August 2017 to March 2018. Preparation and artificial cracking of concrete blocks- The concrete blocks of M20 grade were first prepared with the mould size of 100 mm x 60 mm and left for 28 days curing process. Further, the blocks were subjected to indigenous cracking by plastic shrinkage method (plastic shrinkage cracks usually ranges between 1-2 mm depth) [8] . Determining Size of cracks- Size of the cracks in concrete block was measured using scale [9] . Isolation of new ureolytic bacteria- Soil samples pasteurized at 800 C for 15 minutes then subjected to tenfold dilution. The 0.2 ml of pasteurized diluted sample was then plated on sterile urea agar plates with 5% urea concentration. Plates were incubated at 370 C for 24 - 48 hrs and observed the isolated colonies. Pink color colonies were selected and further screened based on the capability to degrade urea in Christensenโ€™s agar medium and to tolerate high alkaline condition based on pH optimization studies. The single selected potent organism was in turn identified based on its morphological and biochemical characteristics. Latter on the identified isolate was pure cultured on urea agar slants and preserved at low temperature (40 C) [10] . Study on effect of environmental and nutritional condition on urease production a capability of BH3 strains- Bacillus subtilis strain with promising result was selected and the effect of environmental condition like temperature, and nutritional condition such as urea concentration were characterized. For temperature optimization, 1 ml of overnight growth culture was inoculated in 3 tubes containing urease broth except the control tube and incubated at 3 different temperature ranges as 250 C, 350 C, and 450 C then after 24 hours the tubes were observed for change in color intensity and biomass was determined nephlometrically. For urea concentration, optimization purpose 1 ml of overnight growth culture was inoculated in 3 tubes containing urea in concentration range of 2%, 5%, and 10% except the control tube and incubated at 350 C. After 24 hours the tubes were observed for change in color intensity and biomass was determined nephlometrically. [11]
  • 3. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2027 Growth Curve of Bacillus subtilis strains: The growth curve of screened isolate was determined to set a growth comparison point at optimum condition. Three ml of overnight growth culture was used to inoculate in 30 ml of urea broth in 250 ml conical flask then the culture was incubated for 27 hours at 350 C, pH 8, and 5% urea concentration. Inoculation time was considered as zero time and the quantitative determination of growth was carried out by spectrophotometer at 600 nm. Simultaneously the viable cell count was determined as a colony forming units/ml (CFUs) [12] . The desired isolate was purified and mixed with silica gel in 1: 100 dilution factors with the cell count 104 , 105 , 106 cells so as to immobilize the bacterial cells and hence it can remain embedded for the long time in the concrete matrix. Along with it, calcium lactate is also added to it with molar mass 218 g/mole that serve as food source for bacterial cells. As it gets the growth favorable conditions it will soon start to precipitate CaCO3 and the bacterial cells will be in turn coated with it resulting in the autogenous healing [13] . Water Permeability Test of Concrete- To determine the water absorption ability of bacterial concrete, this test was carried out in a comparative manner. For this, the control and bacteria treated concrete blocks were kept overnight saturated in the saline buffer and weighed. Then both blocks were dried in the oven at 1000 C for 24 hours, cooled and again weighed. The obtained values were then put into the formula given below to determine percent water absorption by both the blocks [14] . WSaturation โ€“ WOven Dried % water absorption = WOven Dried Where, WSaturation = Weight of block after saturation WOven Dried= Weight of block after drying RESULTS As the durability of concrete is affected by the cracks leading to corrosion of reinforcing bars, the general method of repairing is time consuming and expensive, so bio based calcite precipitation has been proposed as an alternative and sustainable, environment friendly cracks repair technique. The bio agent selected for this purpose was based on its tolerance to high pH, and continuous formation of dense CaCO3 in the liquid medium. According to analysis and study of blocks by the visual examination of concrete core, the estimated size of cracks varied from 0.3 to 0.5 mm [9] . Total 12 urease positive Bacillus subtilis strains were isolated from soil sample. Out of these 12 isolates Bacillus subtilis BH3 strains were found to be most potent. Optimization- The optimum temperature required for growth of Bacillus subtilis was 350 C. Table 1 and Fig. 1 shows the optimization of temperature by using 3 different temperature ranges. Table 1: Measurement of bacterial growth at 3 different temperature ranges S. No. Bacterial strains Temperature range (0 C) Growth measure Ureolytic activity Interpretation OD600 1. BH3 25 1.51 Color changes to mild pink The maximum ureolytic activity with effective growth was observed at temperature range of 350 C 2. 35 1.52 Color changes to intense pink 3. 45 1.519 Color changes to light pink BH3= Bacillus subtilis The specific urea concentration supporting the growth of selected ureolytic bacterial strains (BH3) was 5%. The Table 2 and Fig. 2 show the effect of urea concentration on the bacterial growth and urea degrading ability of it. X 100
  • 4. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2028 1.505 1.51 1.515 1.52 1.525 25 35 45 Absorbanceat600nm Temperature range (0C) Effectof Temperature on growth of BH3 strain Fig. 1: Effect of temperature on growth of Bacillus subtilis strains Table 2: Measurement of bacterial growth at 3 different urea concentrations 0 0.5 1 1.5 2 2% 5% 10% Absorbanceat600nm Urea concentration Effect of urea concentration on growth of BH3 strain Fig. 2: Effect of urea concentration on growth rate of Bacillus subtilis strains Spectroscopic growth curve- The growth curve of Bacillus subtilis was elucidated using the partially optimized condition. Table 3 and Fig. 3 indicate the growth curve of B. subtilis isolates, which is considered as the selected isolate of this research paper. The maximum OD was seen between 6 to 10 hours and referred as log phase. Nephlometric reading showed that the cultures reached the stationary phase after 10 hours. After 24 hours the bacterial growth was inhibited due to media component depletion and the release of secondary metabolite that may be toxic to viable cells. S. No. Bacterial strains Urea concentration Growth measure Ureolytic activity Interpretation OD600 1. BH3 2% 0.54 Color changes to light pink The maximum ureolytic activity with effective growth was observed at 5% urea concentration 2. 5% 1.75 Color changes to Intense pink 3. 10% 1.69 Color changes to mild pink
  • 5. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2029 Table 3: Nephlometric absorbance values to construct growth curve of screened isolate of B. subtilis 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8 2 1 2 3 4 6 8 9 10 11 12 25 26 27 ODat600nm Hours of incubation Growth curve of strain BH3 Fig. 3: Growth curve of screened potent isolate of B. subtilis strains Studies on concrete crack healing potential of BH3 strains- In this investigation, the 3 concrete blocks, Block 1, Block 2, and Block 3 were used for autogenous healing by the selected strains of Bacillus subtilis. Block 1 with crack size of 0.45 mm width was injected with 105 CFU/ ml along with silica gel and calcium lactate showed the healing of cracks at 21st day of inoculation and the width of crack was reduced to 0.18 mm. Similarly the Block 2 with crack size of 0.52 mm when injected with 106 CFU/ml showed the efficient healing on 19th day of inoculation, whereas the Block 3 with crack size 0.48 mm width, when injected with 104 CFU/ml, showed the healing on 23rd day of inoculation with the reduction in crack size up to 0.25 mm. Absorbance at 600 nm Time in hours Trial 1 Trial 2 Trial 3 Average 1 0.162 0.164 0.180 0.168 2 0.372 0.343 0.417 0.377 3 0.651 0.621 0.682 0.651 4 0.911 1.001 1.073 0.995 6 1.400 1.545 1.521 1.488 8 1.618 1.647 1.690 1.651 9 1.671 1.677 1.700 1.682 10 1.720 1.677 1.710 1.702 11 1.723 1.694 1.721 1.712 12 1.731 1.717 1.729 1.725 25 1.019 1.724 0.940 1.227 26 0.911 0.853 0.848 0.870 27 0.908 0.847 0.769 0.841
  • 6. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2030 Table 4: Concrete crack healing potential of B. subtilis strains in block 1 (105 cells/ml) S. No. Date Initial Characteristics Final characteristic (Width) Interpretation 1. 22nd January Grade: M20 Size: 100 X 60 mm Curing: 28 days Crack developed by: plastic shrinkage type Width: 0.45 mm 0.45 mm Block 1, inoculated with the 105 cells/ml of BH 3 strains, showed the effective healing within 21 days from the day of inoculation 2. 23rd January 0.45mm 3. 24th January 0.44 mm 4. 25th January 0.43 mm 5. 26th January 0.41 mm 6. 27th January 0.4 mm 7. 28th January 0.4 mm 8. 29th January 0.38 mm 9. 30th January 0.37 mm 10. 31st January 0.37 mm 11. 1st February 0.35mm 12. 2nd February 0.34 mm 13. 3rd February 0.31 mm 14. 4th February 0.28 mm 15. 5th February 0.27 mm 16. 6th February 0.25 mm 17. 7th February 0.23 mm 18 8th February 0.2 mm 19. 9th February 0.19 mm 20. 10th February 0.19 mm 21. 11th February 0.18 mm
  • 7. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2031 Fig. 4: Crack healing study in bacteria treated cracked concrete block (Block 1) Table 5: Concrete crack healing potential of B. subtilis strains in block 2 (106 cells/ml) S. No. Date Block characteristics Final characteristic (Width) Interpretation 1. 22nd January Grade: M20 Size: 100 X 60 mm Curing: 28 days Crack developed by: plastic shrinkage type Width: 0.52 mm 0.52 mm Block 2, inoculated with the 106 cells/ml of BH 3 strains, showed the effective healing within 19 days from the day of inoculation 2. 23rd January 0.52 mm 3. 24th January 0.52 mm 4. 25th January 0.518mm 5. 26th January 0.516 mm 6. 27th January 0.514 mm 7. 28th January 0.51 mm 8. 29th January 0.48 mm 9. 30th January 0.47 mm
  • 8. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2032 10. 31st January 0.47 mm 11. 1st February 0.46 mm 12. 2nd February 0.44 mm 13. 3rd February 0.44 mm 14. 4th February 0.4 mm 15. 5th February 0.4 mm 16. 6th February 0.4 mm 17. 7th February 0.39 mm 18. 8th February 0.39 mm 19. 9th February 0.38 mm Fig. 5: Crack healing study in bacteria treated cracked concrete block (Block 2)
  • 9. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2033 Table 6: Concrete crack healing potential of B. subtilis strains in block 3 (104 cells/ml) S. No. Date Block characteristics Final characteristic (Width) Interpretation 1. 22nd January Grade: M20 Size: 100 X 60 mm Curing: 28 days Crack developed by: plastic shrinkage type Width: 0.48 mm 0.52 mm Block 3, inoculated with the 104 cells/ml of BH3 strains, showed the effective healing within 23 days from the day of inoculation 2. 23rd January 0.52 mm 3. 24th January 0.52 mm 4. 25th January 0.518mm 5. 26th January 0.516 mm 6. 27th January 0.514 mm 7. 28th January 0.51 mm 8. 29th January 0.48 mm 9. 30th January 0.47 mm 10. 31st January 0.47 mm 11. 1st February 0.46 mm 12. 2nd February 0.44 mm 13. 3rd February 0.44 mm 14. 4th February 0.4 mm 15. 5th February 0.4 mm 16. 6th February 0.4 mm 17. 7th February 0.39 mm 18. 8th February 0.39 mm 19. 9th February 0.38 mm 20. 10th February 0.26 mm 21. 11th February 0.26 mm 22. 12th February 0.25 mm 23. 13th February 0.25 mm
  • 10. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2034 Fig. 6: Crack healing study in bacteria treated cracked concrete block (Block 3) Water absorption test by using saline buffer- The saline buffer is used in this research work so as to determine the increased resistance of concrete block towards the water penetration and this test was conducted at a laboratory level. According to this test, the normal concrete block had shown the higher water absorption as compared to the concrete block treated with potent ureolytic bacterial BH3 strains. Table 7 numerically represents the bacterial influence on the water permeability of blocks. Table 7: Water saturation test results of bacteria healed cracked concrete Blocks No. Weight (Saturation) Weight (Dried) Water absorption (%) Block 1 192.73 183.70 4.91% Block 2 188.05 174.80 7.58% Block 3 152.30 140.10 8.70% Control 131.1 119.4 9.79%
  • 11. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2035 DISCUSSION This study has revealed the BH3 strains of bacterial species (Bacillus subtilis) isolated from commercial construction sites, have the high ureolytic activity and can tolerate the pH range up to 12, which becomes the primary factor for bio-cementation. Salmabanu L and Suthar G [2] stated this genus of endolithic bacteria can resist the pH range up to 13 and persist for the long duration with efficient ureolytic activity. The isolated and screened potent isolate (BH3) was identified phenotypically and biochemically same as done by Achal et al. [11] and Cheng et al. [15] while the species level characterization was achieved by 16s gene sequencing technique. From the further optimization studies of BH3 strains, it was clear that it shows the effective urea degrading activity at temperature 350 C with 5% urea concentration. Similar conclusion was given by Steubing [12] , who stated that change in temperature and nutritionally sound components can also affect the CaCO3 precipitation efficiency by ureolytic bacteria. Growth curve of this potent strains were determined nephlometrically that showed the log phase of these strains during initial 6-10 hours and become stationary after 10 hours further reduction in the growth rate after 24 hours. The cell count in the range 105 CFU/ml when injected in block 1 with the crack width size of 0.45 mm shows the significant reduction in crack size up to 0.18 in 21 days after inoculation which was more effective as compared to other 2 concrete block injected with 106 and 104 CFU/ml cells. A similar finding was reported by Bai and Varghese [16] during an experimental investigation on the strength properties of fly ash based bacterial concrete. The bacteria treated concrete block shows the significant reduction in its water penetration ability compared to normal concrete block due to the deposition of CaCO3 matrix like structure around the bacterial cells thereby blocking the pores and inhibiting the water percolation through it. As with constant development in the field of civil engineering and increasing CO2 emission, considerable efforts has been devoted to this alternative concept of bio healing of concrete. CONCLUSIONS Our paper describes that due to its self-healing abilities, eco-friendly nature, resistance to water absorption thereby enhancing the strength of building materials along with prevention of steel corrosion, the microbial concrete technology had proved to be better than the conventional technologies. It may also be termed as โ€œSmart Bio Materialโ€. The overall development of strength in bio-concrete is attributed to significant reduction in water absorption capability by using potent bacterial strains of Bacillus subtilis immobilized by means of silica gel and supplemented with calcium lactate as food source. The efficient healing was shown with 105 cells, in block 1 with the reduction in crack size from 0.43 mm to 0.29 mm width at 21st day of inoculation. More exploratory works at large scale should be undertaken to determine the efficacy of bio cementation for consolidations of building. To make the process economical, microbial additives can repaired by industrial growth of cells by employing the products as lactose mother liquor and corn step liquor as nutrient source. Also, the durability of bacterial concrete should be studied under the various weathering conditions. ACKNOWLEDGMENTS The author is grateful to P.G. Department of Microbiology, Dhote Bandhu Science College, India for their help and support in carrying out the present study. Technical assistance and advice was provided by Dr. D. A. Chouhan so I would like to thank him for his encouragement. CONTRIBUTION OF AUTHORS Research concept- Prof. D. A. Chouhan Research design- Prof. D. A. Chouhan Supervision- Prof. D. A. Chouhan Data collection- Diksha H. Jokyani Data analysis and interpretation- Diksha H. Jokyani Literature search- Diksha H. Jokyani Writing article- Diksha H. Jokyani, Prof. D. A. Chouhan Critical review- Prof. D. A. Chouhan Article editing- Prof. D. A. Chouhan Final approval- Prof. D. A. Chouhan REFERENCES [1] Jayaraj G, Tapsi MS. Self-Healing of Concrete Using Polymer Technique. International Journal of Recent Engineering and Development, 2017; 2(1): 21-30. [2] Salmabanu L, Suthar G. A Review on Self-Healing Concrete. Journal of Civil Engineering Research, 2015; 5(3): 53-58.
  • 12. Int. J. Life. Sci. Scienti. Res. eISSN: 2455-1716 Jokyani and Chouhan, 2018 DOI:10.21276/ijlssr.2018.4.5.10 Copyright ยฉ 2015 - 2018| IJLSSR by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 04 | Issue 05 | Page 2036 [3] Dinesh S, Shanmugapriyan R, Namitha Sheen ST. A Review on Bacteria-Based Self-Healing Concrete. Imperial Journal of Interdisciplinary Research, 2017; 3(1): 2454-1362. [4] Jonkers HM, Thijssen A, Copuroglu O, Schalangen. Application of bacteria as self-healing agent for the development of sustainable concrete. Proceedings of the 1st International Conference on Bio. Geo. Civil Engineering, 2008; 36(2): 230-235. [5] Santhosh K, Ramachandran SK, Ramakrishnan V, Bang S. Remediation of concrete using microorganisms. American Concrete Institute Materials Journal, 2001; 98: 3-9. [6] Bang SS, Galinat JK, Ramakrishnan V. Calcite precipitation induced by polyurethane-immobilized Bacillus pasteurii. Enzyme and Microbial Technology, 2001; 287(4): 404-409. [7] Reinhardt HW, Joo M. Permeability and self-healing of cracked concrete as a function of temperature and crack width. Cement and Concrete Research, 2003; 33: 981-985. [8] Dick J, De. Windt W, De Graef B, Saveyn H, Vander Meeren P, De Belie N, Verstraete W. Bio-deposition of a calcium carbonate layer on degraded limestone by Bacillus species, Biodegradation, 2006; 17(4): 357-367. [9] Shetty MS. Concrete Technology theory and practice. Revised ed., India; Schand publication: 2006; p. 361- 362. [10]Sahmaran M, Keskin SB, Ozerkan G, Yaman IO. Self healing of mechanically-loaded self consolidating concretes with high volumes of fly ash. Cement and Concrete Composites, 2008; 30(10): 872-879. [11]Achal V, Mukherjee A, Reddy S. Characterization of two urease-producing and calcifying Bacillus spp. isolated from cement. J. Microbiol. Biotechnol, 2010; 20(11): 1571โ€“1576. [12]Steubing P. Isolation of an Unknown Bacterium from Soil. Proceedings of the 14th Workshop/Conference of the Association for Biology Laboratory Education (ABLE), 1993; p. 240. [13]Kantha DA, Sathyanarayanan KS, Darshan BS, Raja RB. Studies on the characterization of Biosealant properties of Bacillus sphaericus. International Journal of Engineering Science and Technology, 2010; 2(3): 270-277. [14]Irwan JM, Faisal Alshalif A, Othman N, Anneza LH. Effect of Ureolytic Bacteria on Compressive strength and Water Permeability on Bio-concrete. International Conference on Civil, Architectural, Structural and Construction Engineering, 2015. [15]Cheng L, Cord-Ruwisch R. In situ soil cementation with ureolytic bacteria by surface percolation. Ecological Engineering, 2012; 42: 64-72. [16]Bai CP, Varghese S. An experimental investigation on the strength properties of fly ash based bacterial concrete. International Journal of Innovative Research in Advanced Engineering, 2014; 3(8): 64-69. Open Access Policy: Authors/Contributors are responsible for originality, contents, correct references, and ethical issues. IJLSSR publishes all articles under Creative Commons Attribution- Non-Commercial 4.0 International License (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/legalcode