20 research outputs found
Soil health -- a new challenge for microbiologists and chemists.
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Soil health—a new challenge for microbiologists and chemists
Soil health refers to the biological, chemical, and physical features of soil that are essential to long-term, sustainable agricultural productivity with minimal environmental impact. Thus, soil health provides an overall picture of soil functionality. Although it cannot be measured directly, soil health can be inferred by measuring specific soil properties (e.g. organic matter content) and by observing soil status (e.g. fertility). There is also increased interest in studying soil microorganisms in their particular environments, as microbial diversity is intimately related to soil structure and function. One of the key objectives in determining soil health is to acquire indicators that can be used to evaluate the soil’s current status and hence to develop sustainable agricultural systems. In this regard, significant progress has been made over the last few years in the development of specific biomarkers and macromolecular probes, enabling rapid and reliable measurements of soil microbial communities. In addition, modern molecular biological techniques, such as fluorescence in situ hybridization (FISH), reverse transcriptase polymerase chain reaction (RT-PCR), denaturing gradient gel electrophoresis (DGGE), and terminal restriction fragment length polymorphism (T-RFLP), have facilitated the analysis of microbial biodiversity and activity, whereas the application of modern analytical techniques, such as nuclear magnetic resonance (NMR) and pyrolysisgas chromatography-mass spectrometry (Py-GC-MS), have provided data on soil chemistry. The combination of these two approaches offers promise in determining soil health status. [Int Microbiol 2005; 8(1):13-21
Valorization of soda lignin from wheat straw solid-state fermentation: Production of oleogels.
This work describes the solid-state fermentation(SSF) of wheat straw with Streptomyces sp. MDG147 and further soda-pulping process to obtain wheat straw soda lignins(WSLs). Subsequently, these WSLs were NCO-functionalized with 1,6-hexamethylene diisocyanate and then dispersed in castor oil to achieve stable oleogels. The WSLs were characterized using standard analytical methods, gel permeation chromatography, Fourier transform infrared spectroscopy,differential scanning calorimetry, and thermogravimetric analysis. Rheological properties of oleogels were determinedby means of small-amplitude oscillatory shear and viscous flow measurements. The enzymatic profile and production oflignin−carbohydrate complexes were recorded along the growth time of Streptomyces, whose life cycle was achieved after 7 days. NCO-functionalized WSL was able to chemically interact with castor oil via urethane bonding, providing oleogels with suitable rheological characteristics. Linear viscoelastic functions and viscosity values of oleogels were higher when wheat straw was submitted to SSF using Streptomyces, turning out in stronger oleogels.Ministerio de Economía, Industria y Competitivida
Detoxification of azo dyes by a novel pH-versatile, salt-resistant laccase from Streptomyces ipomoea
A newly identified extracellular laccase produced by Streptomyces ipomoea CECT 3341 (SilA) was cloned and
overexpressed, and its physicochemical characteristics assessed together with its capability to decolorize and detoxify an azotype
dye. Molecular analysis of the deduced sequence revealed that SilA contains a TAT-type signal peptide at the N-terminus
and only two cupredoxine domains; this is consistent with reports describing two other Streptomyces laccases but contrasts
with most laccases, which contain three cupredoxine domains. The heterologous expression and purification of SilA
revealed that the homodimer is the only active form of the enzyme. Its stability at high pH and temperature, together with its
resistance to high concentrations of NaCl and to typical laccase inhibitors such as sodium azide confirmed the unique properties
of this novel laccase. The range of substrates that SilA is able to oxidize was found to be pH-dependent; at alkaline pH,
SilA oxidized a wide range of phenolic compounds, including the syringyl and guayacil moieties derived from lignin. The
oxidative potential of this enzyme to use phenolic compounds as natural redox mediators was shown through the coordinated
action of SilA and acetosyringone (as mediator), which resulted in the complete detoxification of the azo-type dye Orange II.This work was financially supported by the
Spanish Ministry of Science (CICYT Project CTQ2004-0344/PPQ to MEA
and BFU 2006-00972/BMC to JMD). We thank the Autonomous Government
of Madrid and the University of Alcalá for the fellowship awarded to
R.M
Paper mill effluent decolorization by fifty Streptomyces strains.
Fifty actinomycete strains isolated from lignocellulosic substrates were examined for the ability to remove the color from a paper mill effluent obtained after semichemical alkaline pulping of wheat straw. Streptomyces sp. strains UAH 15, UAH 23, UAH 30, and UAH 51 were selected for their ability to decolorize the effluent in a liquid medium containing 1% (wt/vol) glycerol, 0.2% (wt/vol) ammonium sulfate, and 80% (vol/vol) effluent. The highest levels of decolorization achieved after the strains grew were 60 to 65%. Strains UAH 30 and UAH 51 were selected for further study because of their different patterns of effluent decolorization during growth. Fractionation of the decolorized effluent by gel permeation chromatography demonstrated that there were reductions in the levels of absorbance of the high- and medium- molecular-weight compounds. These fractions were mainly responsible for the color of the effluent, while the last fractions, the low-molecular-weight compounds, could have been responsible for the residual color of the decolorized effluent. Thin-layer chromatography revealed significant differences among the patterns of bands corresponding to the acidified supernatants obtained after precipitation of alkali-lignin from the effluent samples decolorized by different Streptomyces strains
EVALUATION OF A NEW LACCASE PRODUCED BY STREPTOMYCES IPOMOEA ON BIOBLEACHING AND AGEING OF KRAFT PULPS
The aim of this work is to prove the suitability of a new alkaline and halo-tolerant bacterial laccase (SilA) produced by Streptomyces ipomoea CECT 3341 to enhance the conventional chemical bleaching process of an industrial eucalyptus kraft pulp. The laccase used for this study was a recombinant laccase obtained from cultures of E. coli BL21 (DE3) grown in LB liquid medium. The biobleaching experiment was carried out on Eucalyptus globulus kraft pulps using the above mentioned laccase and acetosyringone as natural mediator. Then, an alkaline extraction and further hydrogen peroxide steps were applied to evaluate the efficiency of the laccase-mediator system as a pretreatment in the bleaching sequences. Biobleached pulps showed a kappa number decrease and a brightness increase without decreasing the viscosity values significantly. Also, a reduction in the consumption of hydrogen peroxide was observed when the enzymatic treatment was applied to the pulp. CIE L*a*b* and CIE L*C* color coordinates measured in pulps demonstrated that among all treatments applied to pulps, the laccase-acetosyringone system presented the best optical properties even after an accelerated ageing process. Finally, it is also remarkable that during this treatment 64% of the laccase activity remained unaltered