Extracellular polymeric substances govern the development of biofilm and mass transfer of polycyclic aromatic hydrocarbons for improved biodegradation

Bioresource Technology

Volumn 193, Issue , 2015, Pages 274-280

  Zhang, Yinping ^a,b   Wang, Fang ^a   Zhu, Xiaoshu ^b   Zeng, Jun ^a   Zhao, Qiguo ^a   Jiang, Xin ^a  

^a INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

^b NANJING NORMAL UNIVERSITY   (China)

Author keywords

Biodegradation; Biofilms; Extracellular polymeric substances (EPS); Polycyclic aromatic hydrocarbons (PAHs)

Indexed keywords

ANTHRACENE; AROMATIC COMPOUNDS; AROMATIC HYDROCARBONS; AROMATIZATION; BACTERIA; BIOCHEMISTRY; BIODEGRADABLE POLYMERS; BIODEGRADATION; BIOFILMS; HYDROCARBONS; MASS TRANSFER; MICROBIOLOGY; POLYMERS; PYRENE;

BACTERIAL ATTACHMENT; BIODEGRADATION EFFICIENCY; BIODEGRADATION RATE; ENHANCED BIODEGRADATION; EXTRACELLULAR POLYMERIC SUBSTANCES; KEY FACTORS; MICROCOCCUS SP; POLYCYCLIC AROMATIC HYDROCARBONS (PAHS);

POLYCYCLIC AROMATIC HYDROCARBONS;

EXTRACELLULAR POLYMERIC SUBSTANCE; PHENANTHRENE; POLYCYCLIC AROMATIC HYDROCARBON; POLYMER; PYRENE; UNCLASSIFIED DRUG; HUMIC SUBSTANCE; HUMIN; PHENANTHRENE DERIVATIVE; PYRENE DERIVATIVE;

BACTERIUM; BIOAVAILABILITY; BIODEGRADATION; BIOFILM; BIOTECHNOLOGY; CORRELATION; EXOPOLYMER; EXTRACTION METHOD; MASS TRANSFER; MICROBIAL ACTIVITY; PAH; PHENANTHRENE; PYRENE;

ARTICLE; BACTERIAL CELL; BACTERIAL STRAIN; BACTERIUM ADHERENCE; BIOAVAILABILITY; BIOFILM; BIOMASS; DEGRADATION KINETICS; LIQUID LIQUID EXTRACTION; MICROBIAL DEGRADATION; MICROCOCCUS; MYCOBACTERIUM; NONHUMAN; POLYMERIZATION; PRIORITY JOURNAL; SURFACE PROPERTY; WASTE WATER MANAGEMENT; BIOREMEDIATION; GROWTH, DEVELOPMENT AND AGING; HUMIC SUBSTANCE; METABOLISM; MICROBIOLOGY;

BACTERIA (MICROORGANISMS); MICROCOCCUS SP.; MYCOBACTERIUM SP.;

BIODEGRADATION, ENVIRONMENTAL; BIOFILMS; BIOLOGICAL AVAILABILITY; HUMIC SUBSTANCES; MICROCOCCUS; MYCOBACTERIUM; PHENANTHRENES; POLYCYCLIC HYDROCARBONS, AROMATIC; POLYMERS; PYRENES;

EID: 84933529788     PISSN: 09608524     EISSN: 18732976     Source Type: Journal    
DOI: 10.1016/j.biortech.2015.06.110     Document Type: Article

References (33)

1. Ayala-Torres C., Hernandez N., Galeano A., Novoa-Aponte L., Soto C.Y. Zeta potential as a measure of the surface charge of mycobacterial cells. Ann. Microbiol. 2014, 64:1189-1195.
2. Baldi F., Pepi M., Capone A., della Giovampaola C., Milanesi C., Fani R., Focarelli R. Envelope glycosylation determined by lectins in microscopy sections of Acinetobacter venetianus induced by diesel fuel. Res. Microbiol. 2003, 154:417-424.
3. Binupriya A.R., Sathishkumar M., Ku C.S., Yun S.I. Sequestration of Reactive Blue 4 by free and immobilized Bacillus subtilis cells and its extracellular polysaccharides. Colloids Surf. B 2010, 76:179-185.
4. Bredholt H., Bruheim P., Potocky M., Eimhjellen K. Hydrophobicity development, alkane oxidation, and crude-oil emulsification in a Rhodococcus species. Can. J. Microbiol. 2002, 48:295-304.
5. Colica G., Li H., Rossi F., Li D., Liu Y., De Philippis R. Microbial secreted exopolysaccharides affect the hydrological behavior of induced biological soil crusts in desert sandy soils. Soil Biol. Biochem. 2014, 68:62-70.
6. Denkhaus E., Meisen S., Telgheder U., Wingender J. Chemical and physical methods for characterisation of biofilms. Microchim. Acta 2007, 158:1-27.
7. Dubois M., Gilles K.A., Hamilton J.K., Rebers P.A., Smith F. Colorimetric method for determination of sugars and related substances. Anal. Chem. 1956, 28:350-356.
8. Frolund B., Griebe T., Nielsen P.H. Enzymatic-activity in the activated-sludge floc matrix. Appl. Microbiol. Biotechnol. 1995, 43:755-761.
9. Frolund B., Palmgren R., Keiding K., Nielsen P.H. Extraction of extracellular polymers from activated sludge using a cation exchange resin. Water Res. 1996, 30:1749-1758.
10. Glazyrina J., Materne E.M., Dreher T., Storm D., Junne S., Adams T., Greller G., Neubauer P. High cell density cultivation and recombinant protein production with Escherichia coli in a rocking-motion-type bioreactor. Microb. Cell Fact. 2010, 9.
11. Gomes I.B., Simoes M., Simoes L.C. An overview on the reactors to study drinking water biofilms. Water Res. 2014, 62:63-87.
12. Jayasinghearachchi H.S., Seneviratne G. Fungal solubilization of rock phosphate is enhanced by forming fungal-rhizobial biofilms. Soil Biol. Biochem. 2006, 38:405-408.
13. Jemaat Z., Suarez-Ojeda M.E., Perez J., Carrera J. Partial nitritation and o-cresol removal with aerobic granular biomass in a continuous airlift reactor. Water Res. 2014, 48:354-362.
14. Johnsen A.R., Karlson U. Evaluation of bacterial strategies to promote the bioavailability of polycyclic aromatic hydrocarbons. Appl. Microbiol. Biotechnol. 2004, 63:452-459.
15. Johnsen A.R., Wick L.Y., Harms H. Principles of microbial PAH-degradation in soil. Environ. Pollut. 2005, 133:71-84.
16. Lehnik-Habrink P., Hein S., Win T., Bremser W., Nehls I. Multi-residue analysis of PAH, PCB, and OCP optimized for organic matter of forest soil. J. Soils Sediments 2010, 10:1487-1498.
17. Misiak K., Casey E., Murphy C.D. Factors influencing 4-fluorobenzoate degradation in biofilm cultures of Pseudomonas knackmussii B13. Water Res. 2011, 11:3512-3520.
18. Neu T.R. Significance of bacterial surface-active compounds in interaction of bacteria with interfaces. Microbiol. Rev. 1996, 60:151-158.
19. Nisha K.N., Devi V., Varalakshmi P., Ashokkumar B. Biodegradation and utilization of dimethylformamide by biofilm forming Paracoccus sp. strains MKU1 and MKU2. Bioresour. Technol. 2015, 188:9-13.
20. Rigano L.A., Payette C., Brouillard G., Marano M.R., Abramowicz L., Torres P.S., Yun M., Castagnaro A.P., El Oirdi M., Dufour V., Malamud F., Dow J.M., Bouarab K., Vojnov A.A. Bacterial cyclic beta-(1,2)-glucan acts in systemic suppression of plant immune responses. Plant Cell 2007, 19:2077-2089.
21. Rodrigues A.C., Wuertz S., Brito A.G., Melo L.F. Fluorene and phenanthrene uptake by Pseudomonas putida ATCC 17514: kinetics and physiological aspects. Biotechnol. Bioeng. 2005, 3:281-289.
22. Rosenberg M. Microbial adhesion to hydrocarbons: twenty-five years of doing MATH. FEMS Microbiol. Lett. 2006, 262:129-134.
23. Sheng G.P., Yu H.Q., Li X.Y. Extracellular polymeric substances (EPS) of microbial aggregates in biological wastewater treatment systems: a review. Biotechnol. Adv. 2010, 28:882-894.
24. Simarro R., Gonzalez N., Fernando Bautista L., Carmen Molina M., Schiavi E. Evaluation of the influence of multiple environmental factors on the biodegradation of dibenzofuran, phenanthrene, and pyrene by a bacterial consortium using an orthogonal experimental design. Water Air Soil Pollut. 2012, 223:3437-3444.
25. Simpson A.J., Song G.X., Smith E., Lam B., Novotny E.H., Hayes M.H.B. Unraveling the structural components of soil humin by use of solution-state nuclear magnetic resonance spectroscopy. Environ. Sci. Technol. 2007, 41:876-883.
26. Sun Y.D., Clinkenbeard K.D., Clarke C., Cudd L., Highlander S.K., Dabo S.M. Pasteurella haemolytica leukotoxin induced apoptosis of bovine lymphocytes involves DNA fragmentation. Vet. Microbiol. 1999, 65:153-166.
27. Tribelli P.M., Di Martino C., Lopez N.I., Iustman L.J.R. Biofilm lifestyle enhances diesel bioremediation and biosurfactant production in the Antarctic polyhydroxyalkanoate producer Pseudomonas extremaustralis. Biodegradation 2012, 23:645-651.
28. Vaiopoulou E., Misiti T.M., Pavlostathis S.G. Removal and toxicity reduction of naphthenic acids by ozonation and combined ozonation-aerobic biodegradation. Bioresour. Technol. 2015, 179:339-347.
29. Wang Z., Wu Z., Tang S. Extracellular polymeric substances (EPS) properties and their effects on membrane fouling in a submerged membrane bioreactor. Water Res. 2009, 43:2504-2512.
30. Wei X., Fang L.C., Cai P., Huang Q.Y., Chen H., Liang W., Rong X.M. Influence of extracellular polymeric substances (EPS) on Cd adsorption by bacteria. Environ. Pollut. 2011, 159:1369-1374.
31. Wolfaardt G.M., Lawrence J.R., Robarts R.D., Caldwell D.E. Bioaccumulation of the herbicide diclofop in extracellular polymers and its utilization by a biofilm community during starvation. Appl. Environ. Microbiol. 1995, 1:152-158.
32. Zhang Y.P., Wang F., Bian Y.R., Kengara F.O., Gu C.G., Zhao Q.G., Jiang X. Enhanced desorption of humin-bound phenanthrene by attached phenanthrene-degrading bacteria. Bioresour. Technol. 2012, 123:92-97.
33. Zhang Y.P., Wang F., Yang X.L., Gu C.G., Kengara F.O., Hong Q., Lv Z.Y., Jiang X. Extracellular polymeric substances enhanced mass transfer of polycyclic aromatic hydrocarbons in the two-liquid-phase system for biodegradation. Appl. Microbiol. Biotechnol. 2011, 90:1063-1071.