Introduction

The global over-dependent on fossil fuels as sources of energy increases the rate and extent of exploration, transportation, refining and storage of crude oil by the petroleum industries1,2. Petroleum industries produce a large amount of leftover from petroleum oil as a residue, which is called petroleum oily sludge (POS). The indiscriminate disposal of inadequately treated oily sludge to the environment is causing a lot of environmental and human health problems. All environmental protection agencies and the experts have classified oily sludge as a hazardous organic waste. Oily sludge is a complex mixture of organic compounds and inorganic metalloids, of which the structure and bioavailability of these compounds resist natural degradation. POS constitutes 50–80% hydrocarbon, 10–30% solid material, 20–30% water and 5–10% heavy metals3. Several physical and chemical methods are being extensively used for the remediation of oily sludge from temporary deposit sites and contaminated environments. However, these methods tend to be expensive and environmentally unfriendly. An alternative is biological methods which can provide an effective and eco-friendly approach. By making use of these kinds of technologies, the content of harmful components is often decreased or eradicated, as well as its negative environmental and health influences can, therefore, be reduced4,5.

Nevertheless, because of the recalcitrant character of POS6, the quest for remediation strategies together with the requirement of fulfilling stringent environmental laws and lowering the cost of remediation is a continuing process3. The complexity of oily sludge composition of hydrocarbon, heavy metals and others made it hardly bioavailable for microbial degradation5. In Malaysia, POS waste falls under the scheduled waste with code SW 311, and about 4,293 tons were generated in 2015 alone (DOE, 2012).

Phytoremediation is one of the strategies of bioremediation, and it uses selected plants to cleanup polluted environment. Plants are more tolerant in general to excessive concentrations of POS compared to microorganisms7. Consequently, phytoremediation is potentially a fresh possibility of a much more effective and sustainable answer for the remediation of POS-contaminated soils8. Numerous plants have already been recognized to assist in the phytoremediation of areas polluted with petroleum hydrocarbons, and great number of research have identified grasses and legumes due to their reportedly greater tolerance to hydrocarbon and also due to their other beneficial qualities9. The plant- microorganisms connection has a tendency to boost the degradation of contaminants in the rhizosphere by way of a symbiotic connection. Plants can promote microbial activity anywhere from 10 to 100 times greater in the rhizosphere through the release of exudates that contain compounds including amino acids, carbohydrates and flavonoids10. The secretion of these nutrients-containing exudates offers nitrogen and carbon sources to soil microorganisms. In addition, this process generates an environment that is nutrient-rich in which the activity of microorganisms can be activated. Along with the capability to secrete compounds that can facilitate the activity and growth of rhizospheric microorganisms, plants can furthermore discharge specific enzymes that have the capability to degrade pollutants. The compounding effect results in a more efficient remediation of toxicants, including POS11.

Legumes are known to have the edge over non-leguminous plants in the process of phytoremediation due to their capacity for nitrogen fixation12 and therefore, do not need to contest with microorganisms as well as other plants for the constrained resources of accessible soil nitrogen. Common desirable characteristics of these plants are the ability to fix nitrogen (a major limiting factor for effective degradation of pollutants) which is strategic to establish nutrient-rich rhizosphere as it is known that areas contaminated with oily sludge have a deficit in the C:N ratio9. The legume-bacterial interaction is a synergistic strategy of which leguminous plants provide the microorganisms in the rhizosphere with growing space and essential nutrients, as the microorganisms use their degrading machinery to biodegrade hydrocarbon pollutant in their surroundings13. Additionally, rhizo- and endophytic microorganisms, in collaboration with the legume improve the supply of nutrient and growth hormones that can promote plants’ growth, and at the same time increase hydrocarbon bioavailability14,15,16,17. Cajanus cajan (pigeon pea) is also known as Kacang dhal in Malay. It is a very common legume crop in tropical countries. The plant provides an important source of protein to the diet of human. It features a lengthy root system which could endure in various soil types18. It can withstand the alterations in pH over a broad range. In addition, the plant is known to grow at a broad range of temperature from 10 to 35 °C19. In India, this plant is utilized as a multi-purpose plant in the agroforestry industry, in which its many functions include as sources of firewood, manure, food and fodder19. Although the plant species utilized in this study has been documented to degrade polluted soil contaminated with spent engine20, no prior research has documented its use in the remediation of POS-contaminated soil. In this study, we report for the first time, the phytoremediation of POS in soil using Cajanus cajan.

Materials and Methods

Experimental setup

The experiment was carried out in the Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia. The petroleum oily sludge (POS) used in this study was obtained from a Shell refinery center in Port Dickson, Negeri Sembilan Malaysia in 2014. The POS is in the form of clay mud and black in colour with a pH of 7.1221. The soil was collected from an agricultural farm in Universiti Putra Malaysia. The seeds of C. cajan (Pigeon pea) and plastic pots were obtained from a local grocery company.

Experimental Design

Pot preparation

Soil, which has been previously air-dried and sieved using a 2 mm sieve was placed in each corresponding pot (3 kg), and labelled as contaminated rhizosphere (CR), contaminated non-rhizosphere (CN), uncontaminated rhizosphere (UR) and uncontaminated non-rhizosphere (UN) (Fig. 1).

Treatment of soil with POS

POS was added into each pot to the final concentrations of 1%, 2%, 3%, 4%, and 5% (w/w) and homogenously mixed. The soil was properly agitated and thoroughly mixed to ensure homogeneity and uniformity of soil to the POS in a fume hood. The pots were allowed to remain undisturbed for one week for the volatilization processes. The soil sample was taken for physicochemical analysis before treatment. After one week, seeds of C. cajan were planted accordingly. Three independent experiments were carried out.

Planting of Seeds

Seed viability test and breaking of dormancy

The viability of the seed of C. cajan was tested using the floatation method. The seeds were tested for viability by soaking it in distilled water for 5 min. After that, all floating seeds are sieved out as non-viable and the water was drained immediately from the seeds that sank which are now considered viable seeds. The seeds were then surface sterilized with 10% hydrogen peroxide solution before planting. The seeds was sown to a depth recommended for C. cajan, which is from 1.5 to 3 cm22. For an excellent establishment of the plants, five seeds were planted in a hole. Likewise, the respective pots were irrigated every day and emergence was observed subsequently. The plants were moderately watered every two days with tap water. The appearance of the plants in response to the presence of POS in soil was monitored to determine if there is any phytotoxicity of POS to the plants.

Microbiological analysis

The media used were Nutrient Agar (NA); for the enumeration and isolation of bacteria, mineral salts media and a modified Bushnell and Haas media the for isolation of hydrocarbon-utilizing bacteria referred to here as oil agar (OA) where diesel oil (0.1% w/v) was used as the carbon source in the medium23.

Culture dependent microbial analysis

The bacterial population of the soil samples for 0, 30, 60, and 90 days was enumerated by serially diluting 1 g of soil sample collected from the rhizosphere of C. cajan. Suitably diluted samples (10−5, 10−6 and 10−7) were transferred into the already prepared media using a dropper pipette, 500 µL of each dilution was inoculated on NA and OA which contained 0.1% v/v diesel agar surface23. The plates were incubated at 30 °C for 24 h, for NA, and five days for OA, respectively23. The number of viable total heterotrophic rhizobacteria and hydrocarbon-utilizing bacteria in the soil samples was estimated from the number of colonies formed using a colony counter.

Culture-independent microbial analysis

Culture-independent bacterial community in C. cajan rhizosphere after 90 days was determined using metagenomics analysis of the rhizospheric soil collected from the contaminated rhizosphere CR of 3% oily sludge and contaminated non-rhizosphere CN of 3% oily sludge as control.

Soil extraction and PCR amplification

Microbial DNA was extracted from samples in treatments CN3 and CR3 after 90 days using Power soil® DNA Isolation Kits (MOBIO, USA) following the manufacturer’s instruction. The marker region of the bacteria was amplified by PCR using a PCR (BioRad Thermal Cycler, United Kingdom) with the following conditions; 95 °C for 2 min, followed by 25 cycles at 95 °C for 30 s, 55 °C for 30 s, and 72 °C for 30 s, and a final extension for 5 min using the primers sequences 5'- barcode 2 - (reverse primer sequence) −3'and 5'-barcode 1- (forward primer sequence) – 3', where the barcode consists of an eight-base sequence that is sample-specific and distinctive to each sample. The PCR reaction was carried out in triplicate 20 µL-mixtures containing 2 µL of 2.5 mM dNTPs, 4 µL of 5 × FastPfu buffer, 0.4 µL of FastPfu Polymerase, 0.8 µL of each primer (5 µM) and 10 ng of template DNA. Extraction of amplicons was carried out from a 2% agarose gel. Purification of the amplicons was carried out utilizing AxyPrep DNA Gel Extraction Kit (Axygen Bioscience, Union City, CA, USA) in accordance to the instruction furnished by the manufacturer and quantified using QuantiFluorTM –ST (Promega, USA). Construction of the library was carried out utilizing Linked ‘Y’ adapter; with adapter dimer removed by utilizing beads and the library was concentrated via PCR and hydroxides utilized in the generation of single-stranded DNA fragments. Sample libraries were then pooled in equimolar concentrations, and paired-end sequenced using the Illumina MiSeq platform (2 × 250/300 bp) according to standard protocols.

Data analysis

Several criteria were utilized for demultiplexing raw Fasta files and QIIME-based quality-filtration (version 1.9.1). The criteria include overlapped relationship and merging of paired-reads into a single read. The merged reads were then utilized for the clustering of operational taxonomic units (OUT), classification of taxonomy and assessment of community diversity. The software Trimmomatic was utilized for processing sequence reads24, and then the reads were assembled utilizing the software Flash25 followed up by more analysis using the software MOTHUR v 1.33.026. Alignment of unique sequences was based to the SILVA database with the settings put to default. In addition, removal of chimeric sequences was carried out. Obtained sequences that passed the screening process were then classified using the Ribosomal Database Project naïve Bayesian rRNA classifier at a confidence of 80%. The proportion of sequence identities was calculated at each taxonomic level as the percentage of all sequences classified in that particular sample. Classification of OTUs was based on the similarities of 97%. The software MOTHUR was utilized in the classification of the alpha-diversity indices, which include observed OTUs (Sobs), Ace, Chao, Shannon and InvSimpson indices. PCoA or principal coordinates analysis conducted in R (Version 3.1.2) was utilized to find the bacterial community structure, which is based on the OTU composition.

Measurement of biodegradation in the soil

Gravimetric method

Five grams of soil from all treatments were collected and transferred into 100 mL conical flasks. Then 50 mL of hexane was added and shaken on a Protech orbital shaker (USA) at 150 rpm for 24 h. The layer separating the solvent with oil and the soil was transferred to a pre-weighted clean conical flask, the sample was left overnight in a fume hood for the evaporation of the solvent, and the amount of residual TPH was gravimetrically determined using the formula.

$$\% \,{\rm{Biodegradation}}=\frac{{\rm{Weight}}\,{\rm{of}}\,{\rm{oil}}\,({\rm{control}})\,-\,{\rm{Weight}}\,{\rm{of}}\,{\rm{oil}}\,({\rm{degraded}})}{{\rm{Weight}}\,{\rm{of}}\,{\rm{oil}}\,({\rm{control}})}\times 100$$

Results and Discussion

Total heterotrophic rhizosphere bacterial count

The total counts for the heterotrophic rhizospheric bacteria (THRB) were enumerated at 0, 30, 60 and 90 days of treatments at various concentrations of POS. The result shows that for 1% POS, the THRB counts for contaminated rhizosphere or CR increased significantly (p < 0.05) but slightly from 125 × 107 to 148 × 107 CFU/g, while the count for contaminated non-rhizospheric CN decreased significantly (p  <  0.05) from 112 × 107 to 77.3 × 107 CFU/g, the counts for the uncontaminated rhizosphere UR stayed about the same from 243 × 107 to 241 × 107 CFU/g and the counts for the uncontaminated non-rhizosphere UN decreased significantly (p  <  0.05) from 202 × 107 to 157 × 107 CFU/g (Fig. 2(a)).

The THRB counts for the 2% POS concentration from 0 to 90 days show a significant (p < 0.05) increase in rhizospheric CR counts from 12.7 × 107 to 144.8 × 107 CFU/g, no significant change (p > 0.05) to the contaminated non-rhizospheric CN count (from 66.3 × 107 to 44.7 × 107 CFU/g), no significant change (p > 0.05) to the uncontaminated rhizospheric UR count (243 × 107 to 232 × 107) CFU/g and also no significant change (p > 0.05) to the uncontaminated non-rhizospheric UN count (from 221 × 107 to 219 × 107) CFU/g (Fig. 2(b)).

The THRB counts for the 3% POS concentration from 0 to 90 days show that the contaminated rhizospheric counts CR were increased but not significant (p > 0.05) (from 123 × 107 to 145.4 × 107 CFU/g), the contaminated non-rhizospheric CN counts were not increased significantly (p > 0.05) (from 35.8 × 107 to 31.3 × 107) CFU/g, the uncontaminated rhizospheric UR counts were increased significantly (p < 0.05) from 152 × 107 to 232 × 107 CFU/g, and the THRB counts in the uncontaminated non-rhizosphere UN were also not increased significantly (p > 0.05) (from 202 × 107 to 219 × 107) CFU/g (Fig. 2(c)).

The THRB counts for the 4% POS concentration from 0 to 90 days shows that the contaminated rhizospheric count CR was not significantly increased (from 96.7 × 107 to 112 × 107 CFU/g), the contaminated non-rhizospheric CN counts were decreased significantly (p < 0.05) (from 41.6 × 107 to 23.7 × 107 CFU/g), the uncontaminated rhizospheric UR counts were not significantly (p > 0.05) increased (from 233 × 107 to 232 × 107 CFU/g) and similarly in the uncontaminated non-rhizospheric UN, the bacterial counts were not significantly (p > 0.05) increased (from 200 × 107 to 219 × 107 CFU/g) (Fig. 2(d)). At the highest POS concentration tested (5%), there were a decreasing trend or no change in overall for the THRB counts. For example, for the contaminated rhizospheric CR counts, a decrease was observed (from 57.7 × 107 to 45.4 × 107 CFU/g), but this decrease was not significant (p > 0.05), in the contaminated non-rhizosphere CN counts, a reduction from 23 × 107 to 13.2 × 107 CFU/g was observed and this reduction was significant (p < 0.05). In the uncontaminated rhizospheric UR bacterial count, a reduction from 243 × 107 to 223 × 107 CFU/g was observed, but similarly, this reduction was not significant (p < 0.05) and finally, in the uncontaminated non-rhizospheric UN counts, there were no significant changes (p > 0.05) observed (from 202 × 107 to 200 × 107 CFU/g) (Fig. 2(e)).

In general, the results show a significant (p < 0.05) increase in the numbers of THRB counts in the uncontaminated rhizosphere (UR) compared to the uncontaminated non-rhizospheric (UN) bacterial counts. Although the microbial community in the rhizosphere is about 10–100 times higher than that of the non-rhizosphere10, the increase in the THRB counts in UR compared to UN as found in this study is marginal. As anticipated, the presence of the contaminant POS significantly reduces the number of THRB counts in both of the contaminated rhizosphere (CR) and non-rhizosphere (CN) treatments over the uncontaminated treatments (UN and UR). The microbial counts were much more pronounced in the uncontaminated soil than the contaminated soil because of the inhibitory effects of POS to the microorganism in general in the contaminated soil. However, there was a significant increase in the number of bacterial populations over time in the rhizosphere treatments (CR), as there were higher bacterial counts after 90 days of treatment compared to that of 30 days while a decrease in THRB counts was generally observed in CN. This shows that the presence of C. cajan favours the growth of THRB bacteria in the soil as found in other studies22,27. The result is also supported by a previous finding28, who reported a total decrease in the number of viable heterotrophic bacteria in soil contaminated with oily sludge.

The hydrocarbon utilizing rhizosphere bacteria (HURB) at 1% POS from 0 to 90 days indicated a significant increase (p < 0.05) in bacterial count in all of the treatments such as in the contaminated rhizosphere CR (from 31.3 × 107 to 131 × 107 CFU/g), in the contaminated non-rhizosphere CN (from 28 × 107 to 54 × 107 CFU/g), uncontaminated rhizosphere UR (from 30 × 107 to 86 × 107 CFU/g) and in the uncontaminated non-rhizosphere UN (from 25 × 107 to 58 × 107 CFU/g) (Fig. 3(a)).

In the 2% POS concentration, the HURB counts from 0 to 90 days show a similar increase in counts where the contaminated rhizosphere CR bacterial counts increased significantly (p < 0.05) from 43 × 107 to 136 × 107 CFU/g, no significant increase (p > 0.05) in the contaminated non-rhizosphere CN (from 28 × 107 to 35 × 107 CFU/g), a significant increase (p < 0.05) for the bacterial count in the uncontaminated rhizosphere UR from 38 × 107 to 67 × 107 CFU/g), and a significant increase (p < 0.05) for the bacterial count in the uncontaminated non-rhizosphere UN as well (from 23 × 107 to 46 × 107 CFU/g) (Fig. 3(b)).

Similarly, for the 3% POS concentration, the HURB counts increased significantly (p < 0.05) from 0 to 90 days for all treatments such as in the contaminated rhizosphere CR (from 32 × 107 to 140 × 107 CFU/g), in the contaminated non-rhizosphere CN (from 28 × 107 to 46 × 107 CFU/g), in the uncontaminated rhizosphere UR (from 32 × 107 to 67 × 107 CFU/g) and finally in the uncontaminated non-rhizosphere UN (from 22 × 107 to 43 × 107 CFU/g) (Fig. 3(c)). For the 4% POS concentration, the counts for HURB for CR were significantly increased from 22 × 107 to 115 × 107 CFU/g, while no significant increase (p > 0.05) in the contaminated non-rhizosphere CN was observed from 20 × 107 to 23 × 107 CFU/g. A significant increase was observed for the uncontaminated rhizosphere UR from 17 × 107 to 60 × 107 CFU/g and also for the uncontaminated non-rhizosphere UN from 14 × 107 to 41 × 107 CFU/g (Fig. 3(d)). At the highest concentrations of POS tested (5%) HURB counts increased significantly (p < 0.05) for all treatments. The bacterial counts in the contaminated rhizosphere CR were increased from 11 × 107 to 111 × 107 CFU/g), while the contaminated non-rhizosphere CN counts were increased from 8 × 107 to 22 × 107 CFU/g. In the uncontaminated rhizosphere, the UR counts were increased from 8 × 107 to 60 × 107 CFU/g) and in the uncontaminated non-rhizosphere, the UN counts were increased from 16 × 107 to 38.7 × 107 CFU/g (Fig. 3(e)).

Hydrocarbon-utilizing rhizospheric bacterial counts revealed higher numbers in the contaminated rhizosphere (CR) for all of the POS concentrations tested, although the density tends to decrease as the POS concentration was increased. This result is similar to previous findings29,30,31,32, which include studies on the phytoremediation of soil amended with waste lubricating oil with Jatropha curcaa31 and Hibiscus cannabinus29 where significant increase in hydrocarbon-utilizing bacteria was observed after 30 days of incubation. However, both of these studies require the addition of organic wastes such as brewery spent grain (BSG) and spent mushroom compost (SMC) as additional carbon and nitrogen sources. The results obtained in this work demonstrate the stimulatory effect of rhizosphere to the hydrocarbon-utilizing bacterial population without the need for additional carbon or nitrogen sources.

Considering the complexity of the rhizosphere, a considerable number of microbial communities tend to withstand the toxic effect of the contaminant and are capable of using hydrocarbon as the source of carbon and energy compared to the community in the uncontaminated control. This is similarly reported in a study of epiphytic hydrocarbon-utilizing bacteria where the average number of bacterial density in a given contaminated soil is significantly greater than in the corresponding control, directly indicating that the contaminant is being utilized by the soil bacteria33. The results suggest that microbial enumeration is a direct indicative method to prove the response of microorganisms to hydrocarbons34,35. For a successful and effective phytoremediation process, the bacterial community in the hydrocarbon-contaminated soil must be well connected to the plant’s ability to enhance microbial association in the rhizosphere, resulting in a higher number of hydrocarbon-utilizing bacteria and enhancing their degradative capacity36.

Apart from the presence of petroleum oil which serves as the carbon and energy source, the higher population of hydrocarbon-degrading bacteria in the contaminated soil may also be attributed to the additive effect of the C. cajan roots which release organic compounds to further stimulate the degradation and bacterial growth. The increase in HURB counts in the presence of C. cajans observed in this study are also observed in several similar studies where higher counts of heterotrophic and oil-degrading bacteria were observed in contaminated rhizospheric soil than in the unplanted contaminated soil8,37.

Culture-independent metagenomics analysis

A sum of 59,873 and 59,756 sequences for CN3 and CR3 was found after a sequence optimization method, with an average number of 442.56 and 435.39 sequences for CN3 and CR3, respectively. A sum of 50821 and 47999 reads on CN3 and CR3, respectively, were subsampled from each replicate for further analysis. The calculated bacterial community abundance indices showed an increase in the values for Ace, Cho, Shannon (Shannon-Weaver) and the Simpson’s index in CR3 compared to CN3 (Table 1). In phylogeny, OTU is the most commonly applied microbial diversity unit where OTU is clustered with a cutoff of 97% similarity for the investigation of the abundance of group or species in the microbial community. The difference between CN3 and CR3 was seen in the number of OTU, which were 512 and 650 for CN3 and CR3, respectively, indicating an increase in richness upon the addition of C. cajan. A similar increase in OTU from 48 (control) to 62 (addition of rhizobacteria) is reported during the rhizoremediation of hexachlorobenzene in constructed wetlands38. The coverage indices showed a significant difference in the two treatments. The coverage did not change by much in this study. In general, a reduction in coverage rate indicates higher diversity. In a similar study of rhizoremediation of hexachlorobenzene using T. angustifolia rhizosphere and P. australis rhizosphere in constructed wetlands38, little reduction in the coverage index was observed for T. angustifolia rhizosphere treatment (from 50 to 47.5) while greater reduction in coverage was observed in P. australis rhizosphere soil treatment (from 50 to 29) despite both treatments showing nearly equal efficacy in remediating hexachlorobenzene. This may imply that coverage change alone may not be adequate in describing potential remediating ability of rhizodegraders. Of all the indices used in population diversity studies, the robust Shannon and Simpson indices have been recommended in measuring microbial diversity39, and it was observed that both of the Simpson’s (measured as InvSimpson) and the Shannon values for CR3 were higher than CN3. A change in both indicating an increase in diversity upon the introduction of C. cajan into the contaminated soil, which is a common theme seen in several studies involving phytoremediation using legumes11,38,40. Both measurements of population were lower in CN3, which may be due to the toxic effect of the contaminant on the bacterial community. The shift of soil bacterial community organization is also seen in the metagenomics sequences, and the results showed (Fig. 4a) that the contaminated rhizosphere (CR3) shows a diverse community of bacterial phyla, in comparison to the change of the microbial community structure seen in the contaminated non-rhizosphere (CN3). A lower diversity in CN3 may be the cause of a lower removal rate of petroleum hydrocarbon which has similarly been reported in previous studies40,41 where with an increase in the concentration of the contaminant, this results in an increase in the toxicity which reduces the efficiency of microbial degradation. This shows the important role of plant-like C. cajan, which stabilizes the C:N:P ratio for the effective degradation of hydrocarbon by the microbial community22. On the other hand, some study reported the inability of plant growth-promoting rhizobacteria to acquire nutrient for growth in severely polluted environments41.

The composition and taxonomic analysis of microbiota amplified sequences were categorized into eight phyla (CN3) and ten phyla in (CR3). The overall bacterial composition of the two treatments varied, as the distribution shows a similar variation between the two treatments in the phylum, class, family and genus level distributions, represented by Fig. 4a to d, respectively. This variation in microbial community is also shown by the PCoA plot, which revealed community-level differences between the contaminated non-rhizosphere control (CN3) and contaminated rhizosphere (CR3) microbiota (Fig. 5).

The contaminated non-rhizosphere (CN3) shows a trend of bacterial phylum such as Proteobacteria, Actinobacteria, Acidobacteria, Bacteroidetes, Firmicutes, Chloroflexi, Saccharibacteria and some uncategorized group. The contaminated rhizosphere (CR3) shows Actinobacteria, Proteobacteria, Bacteroidetes, Acidobacteria, Firmicutes, Gemmatimonadetes, Saccharibacteria, Chloroflexi and Verrucomicrobia to be the dominant phyla, and an unclassified group. In both of the treatments, the phylum Proteobacteria constitute the phylum with higher relative abundance accounting for > 60% in CN3 and almost 42% in CR3. In general, the phylum Proteobacteria dominated the communities of CN3 and CR3 at 70% and 42%, respectively. In the CN3, the Proteobacteria was dominated by the genus Rhizobium, Sphingomonas, and Herbaspirillum. The two phyla were not observed in CN3, but the phyla observed were Verrucomicrobia and Gemmatimonadetes. The presence of Verrucomicrobia is an indicator to the rhizospheric effect created by the presence of C. cajan as bacteria from this phylum are mostly found inhabiting grasslands and in subsurface soil horizons, where they were habitually the prevailing bacterial phylum42. Similarly, Gemmatimonadetes tend to dominant in soil with high rhizosphere activities, although their ecology remains poorly understood, and appear to be the dominant phyla in many soil bacterial communities; with bacteria from the phylum Gemmatimonadetes featuring nearly 2% of soil bacterial communities. Nevertheless, very little is understood of their ecology as a result of an insufficient study on the occurrence and ecology of this bacterial group43. The degradation of petroleum oily sludge hydrocarbons, in general, is accredited to indigenous microorganisms which are found in soil, but the presence of C. cajan will stimulate the habitat for the formation of favourable conditions of metabolisms to the microbial communities as demonstrated in this study where the culture-independent metagenomics technique to access a much more in-depth knowledge of the biological processes of petroleum oily sludge degradation during rhizodegradation shows promising results that agrees in principal to what was observed in the experiments.

An assessment at the phylum level identifies the bacteria belonging to the Proteobacteria as the richest community, and the richness was significantly increased. Proteobacteria covers a group of Gram-negative bacteria that have been widely reported to be able to degrade POS41.

Biodegradation of petroleum oily sludge in soil

Gravimetric analysis

The result of oily sludge degradation in the soil shows the effectiveness of C. cajan in plant-microbe bioremediation process. The result of the gravimetric analysis shows that almost 50% biodegradation of the oily sludge was observed at lower concentrations of oily sludge (CR1%, CR2% and CR3%) after 30 days of planting C. cajan (Fig. 6).