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Model of the regulation of activity of immobilized enzymes (amylases) in soil

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Abstract

The preservation of activity of extracellular enzymes in soil is presently associated with their immobilization on organic or inorganic carriers. Enzyme immobilization results, however, in a significant decrease in enzymatic activity. In the present work, the mechanism responsible for promotion of the catalytic activity was revealed, as well as the favorable effect of low-molecular alkylhydrozybenzenes of the class of alkylresorcinols, which are common in soil organic matter, on stability of immobilized enzymes (exemplified by amylases) by their post-translational modification. Optimal conditions (enzyme to sorbent ratio, pH optimum, CaCl2 concentration, and sorption time) for amylase sorption on a biological sorbent (yeast cell walls) were determined and decreased activity of the immobilized enzyme compared to its dissolved state was confirmed. Alkylresorcinols (C7AHB) at concentrations of 1.6 to 80 mM were found to cause an increase of amylase activity both in the case of already sorbed enzymes (by 30%) and in the case of a free dissolved enzyme with its subsequent immobilization (by 50–60%). In both cases, the optimal C7AHB concentration was 16 mM. Amylase stability was determined for C7AHB-modified and unmodified enzymes immobilized on the biological sorbent after two cycles of freezing (–20°C) and thawing (4°C). Inverse dependence was revealed between increasing stability of C7AHB-modified enzymes and an increase in their activity, as well as higher stability of immobilized modified amylases than of the dissolved modified enzyme. Investigation of the effect of C7HOB-modification in the preservation of activity in immobilized amylases after four freeze–thaw cycles revealed: (1) better preservation of activity by the modified immobilized enzymes compared to immobilized ones; (2) differences in the dynamics of activity loss within compared pairs, with activity of immobilized amylases decreasing after the second cycle to a lower level (42%) than activity of the modified immobilized enzymes after the fourth cycle (48%). These results demonstrate that in the preservation of activity of extracellular enzymes in soil both stabilization mechanisms are of importance: immobilization on organic carriers and modification of the enzyme conformation by low-molecular compounds with the functions of chemical chaperones.

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References

  • Allison, S.D. and Jastrow, J.D., Activities of extracellular enzymes in physically isolated fractions of restored grassland soils, Soil Biol. Biochem., 2006, vol. 38, pp. 3245–3256.

    Article  CAS  Google Scholar 

  • Allison, S.D., Gartner, T., Holland, K., Weintraub, M., and Sinsabaugh, R., Soil enzymes: linking proteomics and ecological processes, in Manual of Environmental Microbiology, 3rd ed., Hurst, C., Crawford, R., Garland, J., Lipson, D., Mills, A., and Stetzenbach, L., Eds., Washington: ASM, 2007, pp. 704–711.

    Google Scholar 

  • Allison, S.D., Soil minerals and humic acids alter enzyme stability: implications for ecosystem processes, Biogeochem., 2006, vol. 81, pp. 361–373.

    Article  CAS  Google Scholar 

  • Allison, S.D., Weintraub, M.N., Gartner, T.B., and Waldrop, M.P., Evolutionary economic principles as regulators of soil enzyme production and ecosystem function, in Soil Enzymology, Shukla, G. and Varma, A., Eds., Berlin: Springer, 2011, pp. 229–243.

    Google Scholar 

  • Arsenault, A., Cabana, H., and Jones, J.P., Laccase-based CLEAs: chitosan as a novel cross-linking agent, Enzyme Res., 2011. 376015.

    Google Scholar 

  • Asgher, M., Bhatti, H.N., Ashraf, M., and Legge, R.L., Recent developments in biodegradation of industrial pollutants by white rot fungi and their enzyme system, Biodegradation, 2008, vol. 19, pp. 771–783.

    Article  CAS  PubMed  Google Scholar 

  • Bernfeld, P., Amylases alpha and beta, in Methods in Enzymology, Colowick, S.P. and Kaplan, N.O., Eds., New York: Academic, 1955, vol. 1, pp. 149–158.

    Google Scholar 

  • Burns, R.G., DeForest, J.L., Marxsen, J., Sinsabaugh, R.L., Stromberger, M.E., Wallenstein, M.D., Weintraub, M.N., and Zoppini, A., Soil enzymes in a changing environment: current knowledge and future directions, Soil Biol. Biochem., 2013, vol. 58, pp. 216–234.

    Article  CAS  Google Scholar 

  • Burns, R.G., Interaction of enzymes with soil mineral and organic colloids, in Special Publication no. 19. Interactions of Soil Minerals with Natural Organics and Microbes, Huang, P.M. and Schnitzer, M., Eds., Madison: Soil Sci. Soc. America, 1986, pp. 429–451.

    Google Scholar 

  • Demkina, E., Mulyukin, A., Kozlova, A., Zolotareva, B., and El-Registan, G., Response of amylase activity in buried paleosols and subsoil permafrost to low-molecular-weight compounds, Eur. J. Soil Biol., 2015, vol. 70, pp. 31–37.

    Article  CAS  Google Scholar 

  • Dick, W.A. and Tabatabai, M.A., Kinetics and activities of phosphatase-clay complexes, Soil Sci., 1987, vol. 143, pp. 5–15.

    Article  CAS  Google Scholar 

  • El-Registan, G.I., Mulyukin, A.L., Nikolaev, Yu.A., Stepanenko, I.Yu., Kozlova, A.N., Martirosova, E.I., Shanenko, E.F., Strakhovskaya, M.G., and Revina, A.A., The role of microbial low-molecular-weight autoregulatory factors (alkylhydroxybenzenes) in resistance of microorganisms to radiation and heat shock, J. Adv. Space Res., 2005, vol. 36, pp. 1718–1728.

    Article  CAS  Google Scholar 

  • El-Registan, G.I., Mulyukin, A.L., Nikolaev, Yu.A., Suzina, N.E., Galchenko, V.F., and Duda, V.I., Adaptogenic functions of extracellular autoregulators of microorganisms, Microbiology (Moscow), 2006, vol. 75, no. 4, pp. 380–389.

    Article  CAS  Google Scholar 

  • Fagain, C.O., Enzyme stabilization—recent experimental progress, Enz. Microb. Technol., 2003, vol. 33, pp. 137–149.

    Article  Google Scholar 

  • Gianfreda, L. and Rao, M.A., Potential of extra cellular enzymes in remediation of polluted soils: a review, Enz. Microb. Technol., 2004, vol. 35, pp. 339–354.

    Article  CAS  Google Scholar 

  • Husain, Q. and Ulber, R., Immobilized peroxidase as a valuable tool in the remediation of aromatic pollutants and xenobiotic compounds: a review, Crit. Rev. Environ. Sci. Technol., 2011, vol. 41, pp. 770–804.

    Article  CAS  Google Scholar 

  • Kandeler, E., Characterization of free and adsorbed phosphatases in soils, Biol. Fertil. Soils, 1990, vol. 9, pp. 199–202.

    Article  CAS  Google Scholar 

  • Khomutova, T.E., Demkina, T.S., Kashirskaya, N.N., and Demkin, V.A., Phosphatase activity in the surface and buried chestnut soils of the Volga-Don interfluves, Euras. Soil Sci., 2012, vol. 45, pp. 423–428.

    Article  CAS  Google Scholar 

  • Kozubek, A. and Tyman, J., Resorcinolic lipids, the natural non-isoprenoid phenolic amphiphiles and their biological activity, Chem. Rev., 1999, vol. 99, pp. 1–31.

    Article  CAS  PubMed  Google Scholar 

  • Krupyanskii, Yu.F., Knox, P.P., Loiko, N.G., Abdulnasirov, E.G., Korotina, O.A., Stepanov, S.A., Zakharova, N.I., Nikolaev, Yu.A., El-Registan, G.I., and Rubin, A.B., Influence of chemical chaperones on the properties of lysozyme and the reaction center protein from Rhodobacter sphaeroides, Biophisics, 2011, vol. 56, no. 1, pp. 8–23.

    Article  Google Scholar 

  • Martirosova, E.I., Karpekina, T.A., and El-Registan, G.I., Enzyme modification by natural chemical chaperons of microorganisms, Microbiology (Moscow), 2004, vol. 73, no. 5, pp. 609–615.

    Article  CAS  Google Scholar 

  • Martirosova, E.I., Plashchina, I.G., and El-Registan, G.I., Increasing of the catalytic activity and functionality of hydrolases with alkylhydroxybenzenes, in Application of Modern Biotechnologies in Food IndustryN, Workshop of scientists of Russia and members of ASEA, Hanoi, 2010, pp. 119–128.

    Google Scholar 

  • Nicolucci, C., Rossi, S., Menale, C., Godjevargova, T., Ivanov, Y., Bianco, M., Mita, L., Bencivenga, U., Mita, D.G., and Diano, N., Biodegradation of bisphenols with immobilized laccase or tyrosinase on polyacrylonitrile beads, Biodegradation, 2011, vol. 22, pp. 673–683.

    Article  CAS  PubMed  Google Scholar 

  • Petrovskii, A.S., Deryabin, D.G., Loiko, N.G., Mikhailenko, N.A., Kobzeva, T.G., Kanaev, P.A., Nikolaev, Yu.A., Krupyanskii, Yu.F., Kozlova, A.N., and El-Registan, G.I., Regulation of the functional activity of lysozyme by alkylhydroxybenzenes, Microbiology (Moscow), 2009, vol. 78, no. 2, pp. 144–153.

    Article  CAS  Google Scholar 

  • Plashchina, I.G., Zhuravleva, I.L., Martirosova, E.I., Petrovskiy, A.S., Loiko, N.G., Nikolaev, Yu.A., and El-Registan, G.I., Effect of methylresorcinol on the catalytic activity and thermostability of hen egg white lyzozyme, in Biotechnology, Biodegradation, Water and Foodstuff, New York: Nova Science, 2009, pp. 45–57.

    Google Scholar 

  • Pohlon, E., Marxsen, J., and Küsel, K., Pioneering bacterial and algal communities and extracellular enzyme activities of stream biofilms, FEMS Microbiol. Ecol., 2010, vol. 71, pp. 1039–1104.

    Article  Google Scholar 

  • Quiquampoix, H. and Burns, R.G., Interactions between proteins and soil mineral surfaces: environmental and health consequences, Elements, 2007, vol. 3, pp. 401–406.

    Article  CAS  Google Scholar 

  • Solyanikova, I.P., Mulyukin, A.L., Suzina, N.E., El-Registan, G.I., and Golovleva, L.A., Improved xenobioticdegrading activity of Rhodococcus opacus strain 1cp after dormancy, J. Environ. Sci. Helth. Part B., 2011, vol. 46, pp. 638–647.

    Article  CAS  Google Scholar 

  • Stasiuk, M. and Kozubek, A., Biological activity of phenolic lipids, Cell. Mol. Life Sci., 2010, vol. 67, pp. 841–860.

    Article  CAS  PubMed  Google Scholar 

  • Steinweg, J.M., Sensitivity of microbial community physiology to soil moisture and temperature in an old field ecosystem, Graduate Degree Program in Ecology, Colorado State Univ., Fort Collins, 2011.

    Google Scholar 

  • Van Horn, D., Sinsabaugh, R., Takacs-Vesbach, C., Mitchell, K., and Dahm, C., Response of heterotrophic stream biofilm communities to a gradient of resources, Aquat. Microbial Ecol., 2011, vol. 64, pp. 149–161.

    Article  Google Scholar 

  • Vorobyova, E., Soina, V., Gorlenko, M., Minkovskaya, N., Zalinova, N., Mamukelashvili, A., Gilichinsky, D., Rivkina, E., and Vishnivetskaya, T., The deep cold biosphere: facts and hypothesis, FEMS Microbiol. Rev., 1997, vol. 20, pp. 277–290.

    Article  CAS  Google Scholar 

  • Wackett, L.P., Biomass to fuels via microbial transformations, Curr. Opin. Chem. Biol., 2008, vol. 12, pp. 187–193.

    Article  CAS  PubMed  Google Scholar 

  • Wallenstein, M.D. and Weintraub, M.N., Emerging tools for measuring and modeling the in situ activity of soil extracellular enzymes, Soil Biol. Biochem., 2008, vol. 40, pp. 2098–2106.

    Article  CAS  Google Scholar 

  • Welch, W.J. and Brown, C.R., Influence of molecular and chemical chaperones on protein folding, Cell Stress Chaperones, 1996, vol. 1, no. 2, pp. 109–115.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zvyagintsev, D.G., Vzaimodeistvie mikroorganizmov s tverdymi poverkhnostyami (Interaction of Microorganisms with Solid Surfaces), Moscow: Mos. Gos. Univ., 1973.

    Google Scholar 

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Correspondence to E. V. Demkina.

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Original Russian Text © E.V. Demkina, E.F. Shanenko, Yu.A. Nikolaev, G.I. El’-Registan, 2017, published in Mikrobiologiya, 2017, Vol. 86, No. 2, pp. 217–228.

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Demkina, E.V., Shanenko, E.F., Nikolaev, Y.A. et al. Model of the regulation of activity of immobilized enzymes (amylases) in soil. Microbiology 86, 231–240 (2017). https://doi.org/10.1134/S0026261717020060

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