OALibJOpen Access Library Journal2333-9705Scientific Research Publishing10.4236/oalib.1104016OALibJ-79909ArticlesBiomedical&Life Sciences Business&Economics Chemistry&Materials Science Computer Science&Communications Earth&Environmental Sciences Engineering Medicine&Healthcare Physics&Mathematics Social Sciences&Humanities Isolation, Identification and Degradation Characteristics of Oil Degrading Bacterial Strain YabinZhan1*XinglingTao1ShanwenHe1ShufenSong1JingjingXing1FangminLi2TaoJiang3LianMa1College of Animal Science, Yangtze University, Jingzhou, ChinaCollege of Life Science, Yangtze University, Jingzhou, ChinaCollege of Chemical and Environmental Engineering, Yangtze University, Jingzhou, China* E-mail:1766784675@qq.com(YZ);11102017041011210, October 201724, October 2017 27, October 2017© Copyright 2014 by authors and Scientific Research Publishing Inc. 2014This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/

Objective: The aim of study is to obtain a strain which can effectively degrade oil. Methods: By enrichment, domestication and separation of culture from the sample which comes from Qianjiang Guanghua Oilfield, the pure culture (G-40) was selected from the medium supplemented with oil as the sole source of carbon. The G-40 was preliminarily identified and classified by morphological observation, physiological and biochemical determination and sequence analyses of 16S rDNA. Effects of temperature, pH, oil concentration, salt concentration, inoculation amount, N and P source on the degradation of the oil were studied by single factor test. Meanwhile, the effects of temperature, pH, oil concentration and salt concentration were optimized by orthogonal design. Result: G-40 was isolated and identified as Brevibacillus laterosporus . The orthogonal design showed that the degradation rate of oil could reach 20.81%, 24.34% and 31.15% at 10 d, 20 d and 40 d under the optimal conditions which was 35℃, initial pH 7.3, oil concentration 0.6%, salt concentration 0.5%, inoculum amount 8%, the optimal N and P was (NH 4 ) 2 SO 4 and K 2 HPO 4 . Conclusion: This study provides microbial resources for bioremediation of petroleum contaminated soil.

Degrading Bacteria Brevibacillus Laterosporus Oil Degrading1. Introduction

Release of hydrocarbon into the environment whether accidentally or due to human activities is a main cause of water and soil pollution [1] [2] . Soil contamination with hydrocarbons causes extensive damage of local system since accumulation of pollutants in animals and plant tissue may cause death or mutations [3] . From the environment, hydrocarbon can also enter in food chains, leading to health problems. In the body, PAH are mutagenic and can cause a decrease in the immune response with an increased risk of infections [4] .

Fortunately, the degradation of these oils in the environment is possible through several techniques: physical [5] , chemical [6] or biological [7] . The technology commonly used for the soil remediation includes mechanical, burying, evaporation, dispersion and washing. However, these technologies are expensive and can lead to incomplete decomposition of contaminants. The process of bioremediation, defined as the use of microorganisms to detoxify or remove pollutants owing to their diverse metabolic capabilities is an evolving method for the removal and degradation of many environmental pollutants including the products of petroleum industry [8] . In addition, bioremediation technology is believed to be noninvasive and relatively cost-effective [9] . Biodegradation by natural population of microorganisms represents one of the primary mechanisms by which petroleum and other hydrocarbon pollutants can be removed from the environment and is cheaper than other remediation technologies and the most efficient for environment safe depollution [10] [11] .

Thus, in order to get insight of the bioremediation process of hydrocarbon in Qianjiang Guanghua Oilfield, the present study focused on the isolation, identification and degradation characterization of indigenous hydrocarbon-degrading bacterial strains with regards to the conditions for optimizing their activities and the efficient cleanup of the hydrocarbon pollutants.

2. Materials and Methods2.1. Source of Isolation

The source for bacterial isolation consisted of soil contaminated with oil. Soil samples were collected into 500 ml sterilized glass bottles from eight sites in Qianjiang Guanghua Oilfield on June 2015, immediately carried to the laboratory and stored in a refrigerator prior at 4˚C to use.

2.2. Media

Oil medium (0.5% oil) according to reference [12] .

Beef peptone liquid medium, beef peptone solid medium, according to reference [13] .

2.3. Isolation of Bacteria

Five gram oil contaminated soil sample was inoculated in the 250 ml erlenmeyer flask of 100 ml oil medium on a horizontal shaker (150 rpm) at 35˚C. After 5 days incubation period, 5 ml of sample from primary enrichment medium was transferred to a fresh oil medium containing the same oil and incubated as above. After three subculturing steps in broth medium, 0.1 ml of enrichment culture was plated after appropriate dilution on beef peptone solid medium and incubated at 37˚C for 24 h. Single colony appeared on the beef peptone solid medium was translated on a fresh beef peptone solid medium and incubated. Pure colony was obtained by using a single colony isolation procedure. Isolated colony was stored at 4˚C on beef peptone solid medium and subcultured at 3-week intervals or mixed with 40% glycerol and stored at −80˚C for future utilization [12] .

2.4. Growth Study

Experiments were conducted in the liquid MS medium described above with 0.5% oil (w/v) as sole carbon and energy source. Growth was monitored by measuring optical density at 420 nm with a TU-1900 spectrophotometer [14] .

2.5. Determination of Petroleum Degradation Rate

The rate of oil degradation was determined by gravimetric method. A total of 80 ml methylene chloride was added to the oil triangle bottle to extract the oil. The water in the oil was dried at room temperature until the anhydrous sodium sulfate column was removed, until the organic solvent completely evaporated. Place the oil in the vacuum drying box at 40˚C and keep the vacuum at 0.04 Mpa for 30 min. Then remove it and leave it in the dryer for 30 min and to weigh. The rate of petroleum degradation is calculated according to the Formula (1):

D = ( C 0 − C S ) C 0 × 100 % (1)

D: The rate of petroleum degradation, %; C0: blank hydrocarbon concentration, mg/L; CS: concentration of petroleum hydrocarbon in the culture fluid, mg/L [15] .

2.6. Taxonomy2.6.1. Culture Characteristics and Cell Morphology

The colony characteristics were observed on the agar plate of Beef Peptone Agar, and the cell morphology was observed under microscope after gram staining.

2.6.2. Physiological and Biochemical Tests

The physiological and biochemical properties of the strain were determined according to the microbiological test method [13] .

2.6.3. Molecular Biological Assay

The16S rDNA gene of colony G-40 was amplified by PCR using the universal primers 27F and 1492R [16] and Thermo Scientific Phusion Flash High-Fidelity kit. The 16S rDNA gene were sequenced by Sangon Biotech (Shanghai, China) Co., Ltd. The sequence similarities were analysed by Blasting on the National Centre for Biotechnology Information (NCBI). The phylogenetic tree was constructed by software MEGA5.0.

2.7. Study on Degradation Characteristics2.7.1. Single Factor Test

The bacteria were inoculated into beef peptone liquid medium. The bacteria were inoculated in logarithmic phase, centrifuged, removed supernatant, washed with sterile normal saline, and adjusted to OD420 = 3.28. In the basic culture medium at the same time, by changing the growth conditions in different temperature, pH, oil concentration, salt concentration, inoculation amount, N source, P source on a horizontal shaker (150 rpm) at 35˚C in 100 ml oil medium for 5 d. Learning the suitable growth conditions of G-40 by the determination of OD420.

2.7.2. Orthogonal Test

Four factors and 3 levels orthogonal test (Table 1) was carried out with temperature, pH and oil concentration and salt concentration. With 8% inoculation on a horizontal shaker (150 rpm) in 100 ml oil medium for 5 d. Learning the optimum growth condition of G-40 by the determination of OD420.

2.7.3. Verification Test

Under orthogonal optimum conditions, the oil removal rate of G-40 was measured at 10, 20 and 40 day, respectively.

2.8. Determination of Growth Curve

Under the optimum conditions, the strain of G-40 was injected into the oil medium with 8% inoculum, drawing the growth curve by measuring its OD420.

3. Results and Analysis3.1. The Results of Taxonomy3.1.1. Culture Characteristics and Cell Morphology

A strain of G-40 which can remove oil isolated from contaminated soil. After 3 days of cultivation of bacteria, colony morphology is shown in Figure 1. A few selected bacteria were Gram staining, showed that bacteria were G+, spores are oval, lateral; The characteristics of colonies are shown in Table 2.

Factor levels table
A (˚C)BC (%)D (%)
1307.30.40.3
2337.50.50.4
3357.70.60.5

A: Temperature; B: pH; C: oil concentration; D: salt concentration.

Morphology and culture characteristics of strain G-40
MorphologyColourTextureProtuberanceEdgeDiameter (mm)Area (mm2)
CircularBeigeSmoothConvex lensIntegrity2.013.13
3.1.2. Physiological and Biochemical

The physiological and biochemical of G-40 is shown in Table 3. Combined with culture characteristics and cell morphology, according to Berger’s Manual of Determinative Bacteriology, the strain can be identified as Brevibacillus [17] .

3.1.3. Molecular Identification

The 16S rDNA gene obtained from the isolates was amplified via PCR using a universal bacterial primer set. Based on the morphological observation, physiological and biochemical determination and sequence analyses of 16S rDNA sequence, the G-40 was identified as Brevibacillus laterosporus. The 16S rDNA sequence date have been deposited in the GenBank database under the accession numbers KY949476. The phylogenetic tree of G-40 showed as Figure 2.

3.2. Physiology3.2.1. Single Factor Test

1) Temperature

The biomass of G-40 was effected by temperature as shown in Figure 3. The biomass increased firstly and decreased lastly with the increase of temperature. There were larger biomass of G-40, when the temperature were 30˚C (OD420 = 0.655) and 35˚C (OD420 = 0.557). Compared with other treatments, there were significant differences.

Extremely significant difference (P < 0.01); Significance difference (P < 0.05). Same as below.

2) pH

The biomass of G-40 effected by pH as shown in Figure 4. The biomass increased firstly and decreased lastly with the increase of pH. There was larger biomass of G-40, when the pH was 7.5 (OD420 = 0.699). Compared with other treatments, there were extremely significant differences.

3) Oil Concentration

The biomass of G-40 effected by oil concentration as shown in Figure 5. There were larger biomass of G-40, when the oil concentration were 0.4% (OD420 = 0.669), 0.6% (OD420 = 0.719), 0.8% (OD420 = 0.615), 1.0% (OD420 = 0.644). Compared with the biomass of oil concentrate 0.2%, there were extremely significant differences.

Biophysiological-biochemical characters of the Strain G-40
Test itemResultTest itemResult
Gelatin liquefaction+Starch hydrolysis−
Indole+Lipid hydrolysis−
H2O2+Ammonia production+
Citrate+Nitrate reduction−
M.R.+Phenylalanine dehydrogenase−
V.P.−H2S+

+: positive, −: negative.

4) Salinity

The biomass of G-40 effected by salt concentration as shown in Figure 6. The biomass increased firstly and decreased lastly with the increase of salt concentration. There were larger biomass of G-40, when the salt concentration were 0.2% (OD420 = 0.482) and 0.4% (OD420 = 0.569). Compared with other treatments, there were extremely significant differences.

5) Inoculation amount

The biomass of G-40 effected by inoculation amount as shown in Figure 7. The biomass increased with the increase of inoculation amount. There were larger biomass of G-40, when the inoculation amount were 8% (OD420 = 0.972) and 10% (OD420 = 1.036). Compared with other treatments, there were extremely significant differences.

6) Nitrogen

The biomass of G-40 effected by nitrogen source as shown in Figure 8. There were larger biomass of G-40, when the nitrogen source were (NH4)2SO4 (OD420 = 0.593), NH4Cl (OD420 = 0.538) and NH4NO3 (OD420 = 0.500). Compared with the biomass of KNO3, there were extremely significant differences.

7) Phosphorus

The biomass of G-40 effected by phosphorus source as shown in Figure 9. There were larger biomass of G-40, when the phosphorus source were K2HPO4 (OD420 = 0.515) and Na2HPO4 (OD420 = 0.534). Compared with the biomass of KH2PO4 and NaH2PO4, there were extremely significant differences.

3.2.2. Orthogonal Test

Different conditions had obvious influence on the oil removal rate of G-40. The maximum range of temperature is the key factor affecting the oil removal rate of G-40, followed by pH and oil concentration, while salt concentration has the least influence. Therefore, the suitable condition of oil removal rate of G-40 was A3B1C3D3which was 35˚C, pH 7.3, oil concentration 0.6%, salt concentration 0.5% (Table 4).

3.2.3. Verification Test

The results of verification test were shown in Figure 10. Under orthogonal optimum conditions, the oil degradation of G-40 reached to 20.81%, 24.34% and 31.15% at 10, 20 and 40 day, respectively.

The orthogonal design and analysis of G-40
TreatmentA (˚C)BC (%)D (%)Result
1307.30.40.30.580
2307.50.50.40.531
3307.70.60.50.487
4337.30.50.50.848
5337.50.60.30.847
6337.70.40.40.554
7357.30.60.41.080
8357.50.40.50.937
9357.70.50.30.798
K10.5330.8360.6890.742
K20.7500.7710.7260.722
K30.9370.6130.8050.756
R0.4040.2230.1160.034

A: Temperature; B: pH; C: Oil concentration; D: Salt concentration.

3.3. Determination of Growth Curve

The results of Determination of growth curve were shown in Figure 11. The 0 - 1 day was the lag phase of G-40; In this period, the reason why no biomass increase is that bacteria were first introduced into a fresh media. The 2 - 11 day was the exponential of G-40; In this period, the strain rapidly propagated and gradually turned the oil medium to muddy. The 12 - 18 day was the stationary phase of G-40; In this period, death rate = rate of reproduction of G-40 and continues for a long time.

4. Discussion and Conclusion4.1. Discussion

Brevibacillus laterosporus was identified by Shida [18] through construction of phylogenetic tree of 16S rDNA gene sequence analysis and Bacillus system in 1996. Based on the morphological observation, physiological and biochemical

determination and sequence analyses of 16S rDNA sequence, the G-40 was identified as Brevibacillus laterosporus.

A strain of G-40 with petroleum as the sole carbon source was isolated from the soil contaminated by petroleum for a long time. The effects of temperature, pH, oil concentration, salt concentration, inoculum amount, N and P source on the degradation of oil were studied. Different conditions had great influences on the oil removal rate of G-40. The G-40 has larger biomass when the inoculation amount was 10% (OD420 = 1.036); Compared with the inoculation amount of 8% (0.972), there was no significant differences; Finally, the inoculation amount 8% was used to do the orthogonal experiment. The optimum N and P source was (NH4)2SO4 and K2HPO4, which is basically consistent with the MS medium. Therefore, the temperature, pH and oil concentration and salt concentration were selected to do orthogonal test to further study the optimum conditions for degrading oil.

The oil removal rate of G-40 reached to 20.81% on 10th day. The oil removal rate of G-40 reached 24.34% on 20th day, increased by 16.96% compared with 10th day. The oil removal rate of G-40 reached 31.15% on 40th day, increased by 27.98% compared with 20th day. Maybe, the nutrition in the bottle had been consumed with the passage of time, the degradation rate of increase was not obvious. In order to improve the oil removal rate, nutrition can be added to the bottle.

Oil degradation is limited by many factors in the soil [14] [19] [20] . The development and utilization of the genetic resources of G-40 bacteria for petroleum degradation and their application in the remediation of petroleum contaminated soils should be further studied.

4.2. Conclusion

The suitable conditions of oil removal rate of G-40 were 35˚C, pH 7.3, oil concentration 0.6%, salt concentration 0.5%, inoculation amount 8%, N and P was (NH4)2SO4 and K2HPO4. Under orthogonal optimum conditions, the oil removal rate of G-40 reached to 20.81%, 24.34% and 31.15% on the 10th, 20th and 40th day, respectively.

Cite this paper

Zhan, Y.B., Tao, X.L., He, S.W., Song, S.F., Xing, J.J., Li F.M., Jiang, T. and Ma, L. (2017) Isolation, Identification and Degradation Character- istics of Oil Degrading Bacterial Strain. Open Access Library Journal, 4: e4016. https://doi.org/10.4236/oalib.1104016

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