Transformation of low molecular compounds and soil humic acid by two domain laccase of Streptomyces puniceus in the presence of ferulic and caffeic acids

Abstract

The two-domain bacterial laccases oxidize substrates at alkaline pH. The role of natural phenolic compounds in the oxidation of substrates by the enzyme is poorly understood. We have studied the role of ferulic and caffeic acids in the transformation of low molecular weight substrates and of soil humic acid (HA) by two-domain laccase of Streptomyces puniceus (SpSL, previously undescribed). A gene encoding a two-domain laccase was cloned from S. puniceus and over-expressed in Escherichia coli. The recombinant protein was purified by affinity chromatography to an electrophoretically homogeneous state. The enzyme showed high thermal stability, alkaline pH optimum for the oxidation of phenolic substrates and an acidic pH optimum for the oxidation of K 4 [Fe(CN) 6 ] (potassium ferrocyanide) and ABTS (2,2 0-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt). Phenolic compounds were oxidized with lower efficiency than K 4 [Fe(CN) 6 ] and ABTS. The SpSL did not oxidize 3.4-dimethoxybenzoic alcohol and p-hydroxybenzoic acid neither in the absence of phenolic acids nor in their presence. The enzyme polymerized HA-the amount of its high molecular weight fraction (>80 kDa) increased at the expense of low MW fraction (10 kDa). The addition of phenolic acids as potential mediators did not cause the destruction of HA by SpSL. In the absence of the HA, the enzyme polymerized caffeic and ferulic acids to macromolecular fractions (>80 kDa and 10-12 kDa). The interaction of SpSL with HA in the presence of phenolic acids caused an increase in the amount of HA high MW fraction and a twofold increase in the molecular weight of its low MW fraction (from 10 to 20 kDa), suggesting a cross-coupling reaction. Infrared and solution-state 1 H-NMR spectroscopy revealed an increase in the aromaticity of HA after its interaction with phenolic acids. The results of the study expand our knowledge on the transformation of natural substrates by two-domain bacterial laccases and indicate a potentially important role of the enzyme in the formation of soil organic matter (SOM) at alkaline pH values.

The Effect of Various Forms of Sulfur on Soil Organic Matter Fractions and Microorganisms in a Pot Experiment with Perennial Ryegrass (Lolium perenne L.)

“…Furthermore, the durability of soil aggregates and the structure of soil are influenced by glomalin-related soil proteins, which are very stable glycol proteins produced in abundance by symbiotic arbuscular mycorrhizal fungi of the genus Glomus [38,39]. Another important part of SOM is also the pool of free phenolic acids (FPAs), products of lignin hydrolysis [40] or humic acids, as well as substrates for the formation of humic substances [37,41,42], which, at certain concentrations, can noticeably weaken or stimulate plant growth [43,44]. In addition to the aforementioned fractions, water-soluble organic carbon (WSOC) and hot-water-soluble organic carbon (HWSOC) are important indicators of early changes in both microbial activity and SOM transformations in soils affected by biotic or abiotic factors [45][46][47][48].…”

Enzyme Activity and Organic Carbon Content in Agricultural Spodosol

“…Они поступают в почву в виде прижизненных выделений корней растений и микроорганизмов (бактерий, актиномицет, грибов) (6,7). ПФО участвуют в биосинтезе гумусовых кислот за счет катализа реакций окислительной полимеризации ароматических соединений в присутствии кислорода (8). Пероксидазы -ферменты, катализирующие окисление полифенолов и некоторых ароматических аминов с участием кислорода перекиси водорода (9,10).…”