Next Article in Journal
A Database of Weekly Sea Ice Parcel Tracks Derived from Lagrangian Motion Data with Ancillary Data Products
Previous Article in Journal
Overview of German Additive Manufacturing Companies
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Data Descriptor

Thermodynamic Data of Fusarium oxysporum Grown on Different Substrates in Gold Mine Wastewater

1
Bioresource Engineering Research Group (BioERG), Cape Peninsula University of Technology, Cape Town 8000, South Africa
2
Department of Chemical Engineering, Cape Peninsula University of Technology, Cape Town 8000, South Africa
*
Author to whom correspondence should be addressed.
Submission received: 14 July 2017 / Revised: 6 August 2017 / Accepted: 14 August 2017 / Published: 15 August 2017

Abstract

:
The necessity for sustainable process development has led to an upsurge in bio-based processes, thereby placing a higher demand on the use of suitable microorganisms. Similarly, thermodynamics is a veritable tool that can predict the behavior of any material under well-defined conditions. Thermodynamic data of Fusarium oxysporum used in the bioremediation of gold mine wastewater, for a process supported with different carbon sources, was investigated. The data were obtained using a Discovery DSC® (TA Instruments, Inc. New Castle, DE, USA) equipped with modulated Differential Scanning Calorimeter (MDSCTM) software. The data revealed minimal differences in the physical properties of the F. oxysporum used, indicating that the utilisation of agro-waste for microbial proliferation in wastewater treatment is as feasible as when refined carbon sources are used. The data will be helpful for the development of environmentally benign process development strategies, especially for environmental engineering applications.
Data Set License: CC-BY

1. Summary

The application of bio-materials and environmentally benign methods including processes has risen due to the impact of industrial waste on the environment. The danger of such waste to both human and ecological systems is well known. Several reports have been published on microbial remediation of industrial wastewater containing cyanide; however, there is minimal commensurate uptake of such technology by the industry despite the LaRonde and Homestake gold mines in Canada, including Gold Fields Limited, demonstrating the feasibility and robustness of such biological process for cyanide remediation [1,2,3]. To date, there are no datasets on physical properties of microorganisms that could be deployed for sustainable environmental engineering applications for free cyanide bioremediation, i.e. in wastewater treatment.
Biological remediation of cyanide-containing wastewater has been dominated by the application of microbial species, namely, fungi, bacteria, algae, and protozoa. Bacterial strains such as Bacillus sp. and Serratia sp. [4,5] as well as fungal strains such as Aspergillus sp. and Fusarium sp. [6,7] have all shown proficiency in utilising cyanide as a carbon and/or nitrogen source. These organisms were grown on whey, coconut shell, Citrus sinensis, and Beta vulgaris, showing the feasibility of the application of agro-waste as a nutrient source for microbial proliferation in cyanide-containing wastewater. Recently, F. oxysporum proliferation was observed to be higher in Beta vulgaris waste compared with glucose [8], a process which was proven to be thermodynamically feasible [9]. Despite the robustness and environmentally friendliness of the microbial remediation of cyanide, chemical treatment methods are still favoured by the industry. This is due to the lack of published information on the impact of cyanide on physical properties of microorganisms. Presently, there is only one report on the thermodynamic data of lyophilized microbial biomass, which used an adiabatic calorimeter to quantify the heat capacity of lyophilized Saccharomyces cerevisiae biomass [10]. However, owing to the irreproducibility of results, preference is given to a differential scanning calorimeter (DSC) over an adiabatic calorimeter in the quantification of thermodynamic properties of biological materials [11,12,13]. Therefore, this study used a differential scanning calorimeter (DSC) equipped with a modulation to measure the thermodynamic properties of dried biomass of Fusarium oxysporum.
This dataset presents the thermodynamic data of lyophilized Fusarium oxysporum biomass harvested over a month in a 1-L, continuously stirred bioreactor containing synthetic gold mine wastewater. Earlier, bioenergetic parameters associated with microbial growth was found to be enthalpically driven for all substrates examined [9]. This data provides further insight into the capability of microorganisms to manage their environment under unfavorable conditions, even when organic waste (agro-waste) is used as the sole supplement to support such a remediation process.

2. Data Description

The thermodynamic property of a material is critical for the prediction of feasibility of any chemical and biological reaction, including processes such as the microbial growth and the biomass conversion of nutrient media to useful products. Thermodynamic properties of biological molecules such as starch, glucose, proteins, and amino acids reportedly measured based on rudimentary heat capacity quantifications and adiabatic calorimetric measurements based on the third law of thermodynamics have been used at low temperatures (0 to 298.15 K); however, there is high uncertainty associated with these estimates [11,13,14].
This data describes the thermal analysis of F. oxysporum grown on different carbon substrates in gold mine wastewater. Fusarium oxysporum, like other cyanide-degrading organisms, have been shown to use different enzymatic pathways to degrade cyanide, depending on the operating conditions (pH, temperature, cyanide concentration) [15,16,17]. Thermodynamic information will substantiate the viability of this enzymatic conversion of cyanide to less hazardous products such as formamide. Tables S1–S3 show data derived from biomass grown on glucose, Beta vulgaris, and Beta vulgaris with free cyanide, respectively. The heat flow and the impact of modulated temperature on heat flow is shown. This can be used to determine the durability of the sample. The heat capacity of the biomass material increased steadily up to 316 K for glucose, 302 K for Beta vulgaris, and 300 K for Beta vulgaris with free cyanide. At 298.15 K, the specific heat capacity from the glucose substrate was found to be highest (0.978 J/g·K). The entropy of the samples can be derived from this heat capacity data over the temperature range including the Gibbs free energy, based on the application of the third law of thermodynamics, since biomasses are not completely crystalline materials.

3. Methods

3.1. Sample Preparation

Fusarium oxysporum was cultivated in gold mine wastewater with carbon sources including glucose, Beta vulgaris, and Beta vulgaris with cyanide, as shown in Akinpelu et al [9]. A sample of dried biomass was resuspended in sterile distilled water in a 1:1, weight:volume ratio and incubated at 298.15 K for 16 h to ferment any residual carbohydrates. An aliquot of the suspension was tested for any residual carbohydrates using the Durham tube method [18]. Once the metabolic activity had ceased, the biomass was centrifuged and lyophilised [10]. All procedures were repeated until a suitable quantity of dry biomass was obtained. The elemental analysis of the dried biomass samples were determined by a Thermo Flash EA 1112 series analyser in a Helium carrier gas (Thermo Fisher Scientific Inc., Waltham, MA, USA), as presented in Akinpelu et al [9].

3.2. Thermal Analysis

Thermal analyses were conducted on a Discovery DSC® (TA Instruments, Inc., New Castle, DE, USA) equipped with modulated Differential Scanning Calorimeter (MDSCTM, New Castle, DE, USA) using a Liquid Nitrogen Cooling Accessory (LNCA, New Castle, DE, USA) at atmospheric pressure. For the purge, helium gas was used at a flow rate of 50 mL/min. Temperature and specific heat calibrations were performed with a MDSCTM certified Indium reference material (Part No. 915061.901) and a sapphire for the specific heat capacity determinations (Part No. 9703790.901), respectively. The MDSCTM equilibrated at a temperature of 123 K and the scans were performed at an underlying heating rate of 3 K/min up to a temperature of 373 K. An amplitude of 1 K and a modulation period of 60 s were used for the sample mass of 2 mg (dry biomass weight). The data were analysed using a TRIOS software v4.1.1.33073 (TA Instruments Inc.,). All procedures were performed in triplicate.

Supplementary Materials

Acknowledgments

The authors acknowledge the funding from the Cape Peninsula University of Technology (CPUT), University Research Fund (URF RK 16).

Author Contributions

E.A. Akinpelu and S.K.O. Ntwampe conceived and designed the experiments; E.A. Akinpelu performed the experiments; S.K.O. Ntwampe and L. Mekuto analysed the data; T.V. Ojumu and S.K.O. Ntwampe contributed reagents/materials/analysis tools; E.A. Akinpelu wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest. The funding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.

References

  1. Du Plessis, C.; Barnard, P.; Muhlbauer, R.; Naldrett, K. Empirical model for the autotrophic biodegradation of thiocyanate in an activated sludge reactor. Lett. Appl. Microbiol. 2001, 32, 103–107. [Google Scholar] [CrossRef] [PubMed]
  2. Stott, M.B.; Franzmann, P.D.; Zappia, L.R.; Watling, H.R.; Quan, L.P.; Clark, B.J.; Houchin, M.R.; Miller, P.C.; Williams, T.L. Thiocyanate removal from saline cip process water by a rotating biological contactor, with reuse of the water for bioleaching. Hydrometallurgy 2001, 62, 93–105. [Google Scholar] [CrossRef]
  3. Huddy, R.J.; van Zyl, A.W.; van Hille, R.P.; Harrison, S.T.L. Characterisation of the complex microbial community associated with the aster™ thiocyanate biodegradation system. Miner. Eng. 2015, 76, 65–71. [Google Scholar] [CrossRef]
  4. Mekuto, L.; Ntwampe, S.; Jackson, V. Biodegradation of free cyanide and subsequent utilisation of biodegradation by-products by Bacillus consortia: Optimisation using response surface methodology. Environ. Sci. Pollut. Res. 2015, 22, 10434–10443. [Google Scholar] [CrossRef] [PubMed]
  5. Singh, N.; Balomajumder, C. Equilibrium isotherm and kinetic studies for the simultaneous removal of phenol and cyanide by use of S. odorifera (mtcc 5700) immobilized on coconut shell activated carbon. Appl. Water. Sci. 2016, 1–15. [Google Scholar] [CrossRef]
  6. Akinpelu, E.A.; Ntwampe, S.K.; Mpongwana, N.; Nchu, F.; Ojumu, T.V. Biodegradation kinetics of free cyanide in Fusarium oxysporum-Beta vulgaris waste-metal (As, Cu, Fe, Pb, Zn) cultures under alkaline conditions. BioResources 2016, 11, 2470–2482. [Google Scholar] [CrossRef]
  7. Santos, B.A.Q.; Ntwampe, S.K.O.; Hamuel, J.; Muchatibaya, G. Application of Citrus sinensis solid waste as a pseudo-catalyst for free cyanide conversion under alkaline conditions. BioResources 2013, 8, 3461–3467. [Google Scholar] [CrossRef]
  8. Akinpelu, E.A.; Ntwampe, S.K.O.; Mekuto, L.; Itoba Tombo, E.F. In Optimizing the Bioremediation of Free Cyanide Containing Wastewater by Fusarium Oxysporum Grown on Beetroot Waste Using Response Surface Methodology. In Lecture Notes in Engineering and Computer Science, Proceedings of the World Congress on Engineering and Computer Science, San Francisco, CA, USA, 19–21 October 2016; Ao, S.I., Douglas, C., Grundfest, W.S., Eds.; Newswood Limited: San Francisco, CA, USA, 2016; pp. 664–670. [Google Scholar]
  9. Akinpelu, E.A.; Ntwampe, S.K.O.; Chen, B.H. Biological stoichiometry and bioenergetics of Fusarium oxysporum EKT01/02 proliferation using different substrates in cyanidation wastewater. Can. J. Chem. Eng. [CrossRef]
  10. Battley, E.H.; Putnam, R.L.; Boerio-Goates, J. Heat capacity measurements from 10 to 300 K and derived thermodynamic functions of lyophilized cells of saccharomyces cerevisiae including the absolute entropy and the entropy of formation at 298.15 K. Thermochim. Acta 1997, 298, 37–46. [Google Scholar] [CrossRef]
  11. Pyda, M. Conformational contribution to the heat capacity of the starch and water system. J. Polym. Sci. Part B Polym. Phys. 2001, 39, 3038–3054. [Google Scholar] [CrossRef]
  12. Pyda, M. Quantitative thermal analysis of carbohydrate-water systems. In The Nature of Biological Systems as Revealed by Thermal Methods; Lörinczy, D., Ed.; Springer Netherlands: Dordrecht, The Netherlands, 2005; pp. 307–332. [Google Scholar]
  13. Boerio-Goates, J. Heat-capacity measurements and thermodynamic functions of crystalline α-d-glucose at temperatures from 10 K to 340 K. J. Chem. Thermodyn. 1991, 23, 403–409. [Google Scholar] [CrossRef]
  14. Kabo, G.J.; Voitkevich, O.V.; Blokhin, A.V.; Kohut, S.V.; Stepurko, E.N.; Paulechka, Y.U. Thermodynamic properties of starch and glucose. J. Chem. Thermodyn. 2013, 59, 87–93. [Google Scholar] [CrossRef]
  15. Akinpelu, E.A.; Adetunji, A.T.; Ntwampe, S.K.O.; Nchu, F.; Mekuto, L. Biochemical characteristics of a free cyanide and total nitrogen assimilating Fusarium oxysporum ekt01/02 isolate from cyanide contaminated soil. Data Brief 2017, 14, 84–87. [Google Scholar] [CrossRef]
  16. Campos, M.G.; Pereira, P.; Roseiro, J.C. Packed-bed reactor for the integrated biodegradation of cyanide and formamide by immobilised Fusarium oxysporum ccmi 876 and Methylobacterium sp. RXM CCMI 908. Enzym. Microb. Technol. 2006, 38, 848–854. [Google Scholar] [CrossRef]
  17. Pereira, P.T.; Arrabaça, J.D.; Amaral-Collaço, M.T. Isolation, selection and characterization of a cyanide-degrading fungus from an industrial effluent. Int. Biodeterior. Biodegrad. 1996, 37, 45–52. [Google Scholar] [CrossRef]
  18. Battley, E.H. The thermodynamics of microbial growth. In Handbook of Thermal Analysis and Calorimetry; Kemp, R.B., Ed.; Elsevier: Amsterdam, The Netherlands, 1999; pp. 219–266. [Google Scholar]

Share and Cite

MDPI and ACS Style

Akinpelu, E.A.; Ntwampe, S.K.O.; Mekuto, L.; Ojumu, T.V. Thermodynamic Data of Fusarium oxysporum Grown on Different Substrates in Gold Mine Wastewater. Data 2017, 2, 24. https://doi.org/10.3390/data2030024

AMA Style

Akinpelu EA, Ntwampe SKO, Mekuto L, Ojumu TV. Thermodynamic Data of Fusarium oxysporum Grown on Different Substrates in Gold Mine Wastewater. Data. 2017; 2(3):24. https://doi.org/10.3390/data2030024

Chicago/Turabian Style

Akinpelu, Enoch A., Seteno K. O. Ntwampe, Lukhanyo Mekuto, and Tunde V. Ojumu. 2017. "Thermodynamic Data of Fusarium oxysporum Grown on Different Substrates in Gold Mine Wastewater" Data 2, no. 3: 24. https://doi.org/10.3390/data2030024

Article Metrics

Back to TopTop