Effect of Crude Oil Polluted Soil and Substrate Quantity on Some Morphological Characters of Pleurotus ostreatus (Jacq.) P. Kumm and Pleurotus pulmonarius (Fries) Quel Fruit Bodies

Onyeizu UR^1,*, Ukoima HN², Chukunda FA² and Nwoko MC³

¹Department of Environmental Management and Toxicology, Michael Okpara University of Agriculture Umudike, Nigeria

²Department of Forestry and Environment, Rivers State University of Science and Technology, Port Harcourt, Nigeria

³Department of Plant Science and Biotechnology, Michael Okpara University of Agriculture Umudike, Nigeria

*Corresponding Author:

Onyeizu UR
Department of Environmental Management
and Toxicology, Michael Okpara
University of Agriculture Umudike, Nigeria
Tel: 2348065189734
E-mail: ur.onyeizu@mouau.edu.ng

Received Date: February 28, 2017 Accepted Date: June 26, 2017 Published Date: June 28, 2017

Citation: Onyeizu UR, Ukoima HN, Chukunda FA, Nwoko MC (2017) Effect of Crude Oil Polluted Soil and Substrate Quantity on Some Morphological Characters of Pleurotus ostreatus (Jacq.) P. Kumm and Pleurotus pulmonarius (Fries) Quel Fruit Bodies. J Bioremediat Biodegrad 8: 401. doi:10.4172/2155-6199.1000401

Copyright: © 2017 Onyeizu UR, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Bioremediation & Biodegradation

Abstract

The study was conducted to determine the influence of different levels of crude oil pollution on some morphological characteristics of P. ostreatus and P. pulmonariusfruit bodies. Crude oil treatment was done at 2%, 4% and 6% levels to 2,500 g/kg of garden soil. A.gayanus substrate was used in two quantity layers of 150 g/kg (4 cm) and 300 g/kg (8 cm) and placed on top of the polluted soil before spawn inoculation. The Cap Size (C.S cm), Stipe Length (S.L cm) and Weight (Wt. g/kg) of each mature mushroom fruit body were determined. Data collected were analysed using Analysis of Variance (ANOVA), while mean separation was done using Duncan Multiple Range Test (DMRT). Results showed that mean and standard error mean (mean± SEM) of C.S, S.L, and Wt of fruit bodies of both oyster mushrooms were not significantly different at p<0.05. Therefore, the various levels of crude oil pollution (2%, 4%, and 6%), as well as A.gayanus substrate layers/quantities of 4 cm/150 g/kg and 8 cm/300 g/kg did not affect some of the morphological characters of the Oyster mushroom species studied.

Keywords

Mushroom; Crude oil; Fungi; Polluted soil

Introduction

The ability of mushrooms to utilize various lignocellulosic substrates, makes their cultivation possible in different parts of the world [1]. Substrate type is one of the major factors affecting the yield and quality of oyster mushroom [2]. A substrate in mushroom cultivation may be defined as a kind of lingo cellulose material which supports the growth, development and fruiting of mushroom [3]. Most of all edible mushroom species can utilize various kinds of substrate materials depending on their availability in different places. The nutrient composition of these substrate materials is one of the factors affecting the saprobiotic colonization of the mycelia of cultivated mushrooms [4].

The growth, quantity and quality of yield of the desired mushrooms depend on the utilization of nutrients and physiochemical environment in the medium or substrate. Therefore, the growth of diverse type of mushrooms requires different type of substrates and availability of varied type of materials may dictate which type is used. Kumar et al. reported the successful cultivation of oyster mushroom on conventional substrates sufficiently available, which are not utilized properly and productively.

Mushrooms and Crude Oil

Several fungi like Pleurotus ostreatus, Lentinus subnudus and Pleurotus tuber-regium have been grown in crude oil mediated substrate [5-7]. Ogbo and Okhuoya [7] showed that P. tuberregium was able to decontaminate crude oil contaminated soils reducing the various petroleum hydrocarbons in crude oil to varying degrees. The contaminants instead of inhibiting the growth of the fungus, enhanced it. The ability of white rot fungi to degrade petroleum hydrocarbons can be due to the fact that these fungi are uniquely equipped as soil remediation agents [8]. White rot fungi are filamentous organisms and as such have the propensity to extend through soil in search of new substrates to exploit and thus colonize larger surface area than bacteria. Furthermore, with the aid of their highly oxidative lignin degrading systems, they are able to oxidize extremely hydrophobic substrates [9]. The only drawback here is that these environmental pollutants or their degradation products may inhibit their lignin degrading system [10,11]. Petroleum hydrocarbons have been shown to improve the growth of white rot fungi in contaminated soils by increasing their cap diameter, stipe length and yield indicating that the contaminants have a fertilizer effect [5,12].

This investigation aims to explore the influence of crude oil pollutant and substrate quantity on some morphological characteristics of P. ostreatus and P. pulmonarius fruit bodies studied.

Materials and Methods

Study area

The study was conducted in the screen house of the Michael Okpara University of Agriculture Umudike, Abia State. Umudike is located between longitude 7° and 70°05°E and latitude 5° and 5°25°N; with humid tropical climate. Rainfall is bi-modally distributed with peaks between July and September of each year. Annual rainfall is approximately 170 mm, spread between April and November each year.

Source of culture and spawn multiplication

Pure mycelia culture of P. ostreatus and P. pulmonarius were obtained and multiplied at the department of biotechnology, Federal Institute of Industrial Research, Oshodi (FIIRO) Lagos State. Spawns were produced using sorghum grains. Sorghum grains were washed and soaked in tap water overnight. Grains were further boiled in same tap water in the ratio of 1:1 (sorghum grain: water) for 15 mins, using the industrial cooking gas as a local heat source. 4% (w/w) CaCO₃ and 2% (w/w) CaSO₄ were added to optimize pH and prevent clumping of grains respectively as described by Muhammad et al. [13]. Completely drained Sorghum grains were stuffed in glass Bama bottles tightly sealed with Aluminium foil and before being sterilized in an autoclave at 121°C for 30 mins. After sterilization, the bottles were allowed to cool, before they were inoculated with actively growing mycelia of P. ostreatus and P. pulmonarius by grain-to- grain transfer and incubated in the dark at (27 ± 2°C) for 10-15 days until the grains were fully colonized by mycelia [14].

Source of pollutant (Crude oil)

The Bonny Light crude oil was obtained from the Nigerian National Petroleum Co-operation. (N.N.P.C.), Port Harcourt.

Bucket preparation

Five-liter transparent plastic buckets were used during this investigation. The upper half of each 5-liter plastic bucket was perforated, with two lateral holes of 5 mm diameter Okulehie and Okwujiako [15].

Source and soil preparation

Loamy soil sample was collected from a farmland within the vicinity of Government College Umuahia, Abia State. Soil sample was collected from the ‘A’ horizon (0-25 cm). To obtain a semi-sterile soil, the soil was treated in three successive pasteurization periods of 2 hrs each, for two consecutive days, following the modified method of Kristanti et al. [16]. The moisture content of the soil was adjusted to 60% of maximum water-holding capacity (WHC; 0.2 ml/g dry soil) after each pasteurization.

Crude oil pollution

Each perforated plastic bucket contained 2.5 kg of pasteurized soil polluted with 50 g, 100 g and 150 g w/v of crude oil to make 2%, 4% and 6% crude oil pollution of the soil.

Source and preparation of substrate

Andropogon gayanus , a locally available straw substrate was obtained from a farmland in Umudike. The grass was dried and chopped into about 1-2 cm lengths before steeping it in tap water overnight to ensure adequate moisture content [17].

The soaked substrate was drained of excess water before being transferred into a metallic drum for pasteurization at 80°C for 2 hrs and was allowed to cool overnight as recommended by Muhammad et al. [13].

Experimental procedure

The experiment was conducted using 2.5 lit plastic bowels. Three levels of crude oil pollution at 50 g, 100 g and 150 g w/v was used to homogenizes each 2500 g of the prepared soil sample to make 2%, 4% and 6% respectively. The various levels of crude oil polluted soil were poured into each perforated transparent plastic bowel while the control was not polluted with crude oil. All the crude oil treatment levels including control were made up of two groups. The first group consist of 4 cm (150 g) thick layer of prepared A.gayanus substrate placed on the surface of the crude oil polluted soil and inoculated with 30 g of grain based spawn of actively growing mycelia of P. ostreatus and P. pulmonarius while the second has 8 cm (300 g) thick layer of same substrate and was inoculated with 60 g grain based spawn of same mushrooms according to a modified method of Okwulehie and Okwujiako [15].

The spawn-inoculated substrate served as a mycelia mat on the surface of the crude oil polluted soil, contained in the buckets [18]. After spawn inoculation, spawn run was completed in the dark by covering the inoculated buckets with thick non-transparent polythene mat, until the substrate is fully colonized by the mycelia. Priormodial initiation was preceded by fruit body maturity before they were finally harvested.

Determination of morphological

Some morphological characteristics of fruit bodies produced on each experimental unit of various percentage crude oil pollution and the control were recorded as follows.

Cap diameter: This was determined by placing a transparent ruler across the center of the pileus of each harvested mushroom fruit body and recording the value.

Length of stipe: This was determined by placing transparent ruler along the length of each fruit body stipe.

Weight of fresh fruit bodies: This was determined by weighing each fresh fruit body immediately after harvesting, using a portable digital balance.

Statistical analysis

All the data collected from various samples were subjected to Analysis of Variance (ANOVA) while comparison between different means were done using Duncan multiple range test (DMRT) at p<0.05 level significance.

Results and Discussion

Discussion

In this work, effect of crude oil pollution and substrate quantity on some morphological characteristics of P. ostreatus and P. pulmonarius fruit bodies was successfully carried out. The results in Table 1 showed that both P. ostreatus and P. pulmonarius were able to grow on A.gayanus substrate of 150 g/4 cm substrate quantity, increase in crude oil pollution led to a gradual decrease in the cap diameter of fruit bodies of both mushrooms. This observation is not in isolation because Eggen and Vaclav [19] also pointed out that concentration of pollutant such as crude oil is one of the factors that leads to fungal growth efficiency in a medium or substrate. The result also reveals that P. pulmonarius produced fruit bodies with bigger cap diameter at all levels of crude oil pollution. This could be as a result of certain inherent or genetic factors in the mushroom which gives it a more cellulose degrading ability due to secretion of certain enzymes like cellulose, lignase, peroxidise etc. [19-21]. Stipe length of the two mushrooms was also evaluated (Table 2). It was observed that increase in crude oil pollution at different levels (2-6%) caused a significant decrease on the stipe length of the fruit bodies of both mushroom species. Carbon is the major component of crude oil and is required by mushrooms during their vegetative stage [3,22]. During fruit body production (i.e., reproductive) stage of mushrooms, oxygen is required for effective fruitification and development of the cap and the stipe [23,24]. This could be the major reasons why increase in crude oil hindered the Morphological development of both fruit bodies [3,21,25] Increase in crude oil pollution also caused a reduction in the fresh weight of fruit bodies of the two oyster mushroom species (Table 3), there was no significant different in the fresh fruit body weight of both mushrooms at various levels of crude oil pollution p<0.05. This observed reduction in fruit body weight with attendant increase in crude oil pollution is synonymous with the decrease in cap diameter and stipe length of the fruit bodies of both mushroom species. This shows that whatever that affects the size of fruit body also affects its weight and general yield across the substrate. This result was in-line with the works of Okwulehis and Okwujiaka [15], Assan and Mpofu [1] who reported that the unit weight of mushroom fruit bodies collected from any substrate determines its yield and Biological efficiency.

Table 1: Effect of crude oil pollution and 150 g/4 cm A. gayanus substrate on the cap diameter of P. ostreatus and P. pulmonarius fruit bodies. Values are means of 3 replicates. Means with the same superscript are not significantly different p<0.05.

Table 2: Effect of crude oil pollution and 150 g/4 cm A. gayanus substrate on the stripe length of P. ostreatus and P. pulmonarius fruit bodies. Values are means of 3 replicates; means with the same superscript are not significantly different p<0.05.

Table 3: Effect of crude oil pollution and 150 g/4 cm A. gayanus substrate on the fresh fruit body weight of P. ostreatus and P. pulmonarius. Values are means of 3 replicates means with the same superscript are not significantly different p<0.05.

Table 4 showed the results of the cap diameter of P. ostreatus and P. pulmonarius fruit bodies harvested from 300 g/8 cm layer of A.gayanus substrate as affected by different levels of crude oil pollution. There was no significant difference at p<0.05 in the sizes of the cap of both oyster mushrooms at 150 g/4 cm (Table 1) and 300 g/8 cm. This shows that quantity of substrate has no significant effect on the size of the cap of both fruit bodies because cap sizes at higher substrate layer (300 g/8 cm) were similar to those of lower substrate layer (150 g/4 cm) (Table 1). This result was in consonance with the works of Assan et al. and Gitte et al. [26] who reported that increase in substrate quantity did not influence the days to fruiting, as well as size of individual fruit body, but may affect the yield and biological efficiency at the end of the fruiting cycle; since biological efficiency is calculated as percentage fresh fruit body yield in relation to the dry weight quantity of substrate [3,12,22].

Table 4: Effect of crude oil pollution and 300 g/8 cm A. gayanus substrate on the cap diameter of P. ostreatus and P. pulmonarius fruit bodies. Values are means of 3 replicates. Means with the same superscript are not significantly different p<0.05

Table 5 also reveals that substrate quantity and crude oil pollution did not significantly affect stipe length of both mushrooms at p<0.05. Unlike the results in Table 2 where P. ostreatus raised across the various levels of crude oil pollution at 300 g/8 cm level of substrate, stipe length of both oyster mushrooms was not significantly different. This could be that higher quantity of substrate is needed to reduce the negative effect of high concentration of crude oil pollution. Therefore, in a highly polluted environment, large quantity (layer) of substrate is needed to reduce the effect of the pollutant. This now brings solution to the problems observed by Eggen and Vaclav [21] stating that one of the factors influencing the effectiveness of fungal soil remediation is the concentration of the pollutant.

Table 5: Effect of crude oil pollution and 300 g/ 8 cm A. gayanus substrate on the stipe length of P. ostreatus and P. pulmonarius fruit bodies. Values are means of 3 replicates. Means with the same superscript are not significantly different p<0.05.

The result of the influence of 300 g/8 cm layer of A.gayanus substrate on the fruit body weight of P. ostreatus and P. pulmonarius was presented in Table 6. The result shows that fruit body weight of P. pulmonarius was clearly affected by crude oil pollution. Increase in crude oil pollution decreased fruit body weight from 2%-6%. A similar result was also observed in P. ostreatus , judging from 0-2%, but did not follow a regular trend at 4- 6%. The result observed in P. ostreatus could be due to other uncontrolled factors such as contaminants which affects mushroom cultivation [3,13,27]. These contaminants may have initially affected the experimental unit of the 4% crude oil pollution and those of 6% or vise versa.

Table 6: effect of crude pollution and 3000 g/8 cm A. gayanus substrate on the fresh fruit body weight of P. ostreatus and P. pulmonarius. Values are means of 3 replicates. Means with the same superscript are not significantly different p<0.05.

Conclusion

Pleurotus ostreatus and P. pulmonarius were successfully cultivated in a crude oil mediated A.gayanus straw substrate of 150 g/4 cm and 300 g/8 cm layers. A general consideration of the result showed that increase in crude oil pollution from 2- 6% affected the cap diameter, stipe length and fruit body weight of the two oyster mushrooms.

It was also observed that substrate quantity of 300 g/8 cm layer reduced the negative effect of crude on the morphological characteristics of both oyster mushrooms, but did not significantly affect their weight.

In any attempt to use P. ostreatus and P. pulmonarius to remediate a polluted soil, one should first determine the quantity or layer of substrate that should form adequate mycelia mat.

Larger quantity or layer of substrate should be used in a highly polluted environment; this will enhance mycelia colonization to overcome the negative influence of the pollutant on fruit body development.

References

1. Assan N, Mpofu T (2014) The influence of substrate on mushroom productivity. Scientific Journal of Crop Science 3: 86-91.
2. Chitamba J, Shamuyarira M, Dube F, Mudada N, Mapurazi S (2012) Evaluation of cotton waste, paper waste and Jatropha cake for culture of Pleurotus sajor-caju under different pasteurization methods.  Int J Agr & Agri R 2: 1-6.
3. Chang ST, Miles PG (2004) Mushroom cultivation, nutritional value, medicinal effect and environmental impact. CRC press, Newyork, USA P: 451.
4. Tshinyangu KK, Hennebert GL (1995) Effects of synthetic nutrient carriers on the fruiting of Pleurotus ostreatus var columbinus. Biores Technol 54: 249-254.
5. Isikhuemhen OS, Anoliefo G, Oghale O (2003) Bioremediation of crude oil polluted soil by the white rot-fungus, Pleurotus tuber-regium (Fr). Sing Environ Sci pollut Res 10: 108-112.  
6. Adenipekun CO, Fasidi IO (2005) Bioremediation of crude-oil polluted soil by Lentinus subnudus, a Nigerian whiterot fungus. Afr J Biotechnol 4: 796-798.
7. Ogbo EM, Okhuaya JA (2008) Biodegradation of aliphatic resinic and aliphatic fractions of crude oil contaminated soils by Pleurotus tuber-regium Fr. Singer a whiterot fungus. Afr J Biotechnol 7: 4291-4297.
8. Reddy CA (1995) The potential for white rot fungi in the treatment of pollutants. Curr Opinion Biotechnol, 6: 320-328.
9. Kirk TK, Farrel RL (1987) Enzymatic combustion: the microbial degradation of lignin. Ann Rev Microbiol 41: 465-505.
10. Fenn P, Kirk TK (1979) Ligninolytic system of Phanerochaete chrysosporium; Inhibition of O-phtalate. Arch Microbiol 123:307-309.
11. Bumpus JA, Tatarko M (1994) Biodegradation of 2, 4, 6- trinitroltoluene by Phanerochaeta chrysosporium: Identification of initial degradation products and the discovery of a TNT metabolite that inhibits lignin peroxidases. Curr Microbiol 28: 185-190. 
12. Stamets P (2005) Mycelium Running: How Mushroom Can Help Save the World. Ten speed Press, California, USA p: 339.
13. Muhammad AA, Muhammad S, Shabbier A, Asif HM (2007) Protein and fat contents of various Pleurotus species raised on different waste materials.  Pak Journal Agri Sci 44: 140-143.
14. Shyam SP, Syed AA, Sureh MT, Mirza MV (2010) The nutritional value of Pleurotus ostreatus (Jacq: Fr) Kumm. Cultivated on different lignocellulosic Agro waste. Innov Rom Food Biotechnol 7: 66-76.
15. Okwulehie IC, Okwujako IA (2008) The use of local Nigerian substrates for the production of Pleurotus ostraetua var florida (Eger) sporohores. Dyn Biochem Process Biotechnol Mol Biol  2: 38-40.
16. Kristanti RA, Tony H, Tadashi T, Yasuhiro T, Kazuhiro M (2011) Bioremediation of Crude Oil by White Rot Fungi Polyporus sp. S133. J Microbiol Biotechnol 21: 995-1000.
17. Sharma BB (2003) Effects of different substrate (grain straws) on spawn growth and yield of Pink oyster mushroom, Pleurotus djamour (Fr) Boediji.  J mycol Pl Pathol 33: 265-268.
18. Fatuyi OE (2014) Comparative Studies on Biodegradative Abilities of Pleurotus ostreatus and P. pulmonarius in Soils Contaminated with Crude and Used Engine Oils. Adv Microbiol 4: 849-855.
19. Sack U, Heinze TM, Deck J, Cerniglia CE, Martens R, et al. (1997) Comparison of phemanthrene and Pyrene degradation by different wood decaying fungi. Appl Environ microbial 63: 3919-3925.
20. Sack U, Fritsche W (1997) Enhancement of pyrene mineralization in soil by wood degrading fungi. FEMS microbiology Ecol 22: 77-83.
21. Eggen T, Sasek V (2002) Use of edible and medicinal oyster mushroom (Pleurotus ostreatus Jacq. Fr.) Kimm spent compost in remediation of chemically polluted soil. Int J Med Mushrooms 4: 225-261.
22. Chang ST (2013) Training manual on mushroom cultivation technology. Asian and Pasific Centre for Agricultural Engineering, Beijing, China pp: 24-122.
23. Oei P (1999) Small scale mushroom cultivation. CTA publishers, Wageningen, Netherlands P: 86.
24. Oei P (2003) Mushroom cultivation: appropriate technology for mushroom growers. Backhuys Publisher, Leiden, Netherland. Pp: 110-150.
25. Stamets P (2000) Growing gourmet and medicinal mushrooms. Ten speed Press, Berkeley, California, USA Pp: 574.
26. Gitte V, Priya J, kotgire G (2014) Selection of different substrate for the cultivation of milky mushroom. (Calocybe indica P and C). Int J Agr Res 7:100.
27. Oei P (1996) Mushroom cultivation with special emphasis on appropriate techniques for developing countries. Tool pub Pp: 52-60.

--