Fungal extracellular enzyme activity

Last updated
Birch polypore (Piptoporus betulinus) - geograph.org.uk - 1553987 Birch Polypore (Piptoporus betulinus) - geograph.org.uk - 1553987.jpg
Birch polypore (Piptoporus betulinus) - geograph.org.uk - 1553987

Extracellular enzymes or exoenzymes are synthesized inside the cell and then secreted outside the cell, where their function is to break down complex macromolecules into smaller units to be taken up by the cell for growth and assimilation. [1] These enzymes degrade complex organic matter such as cellulose and hemicellulose into simple sugars that enzyme-producing organisms use as a source of carbon, energy, and nutrients. [2] Grouped as hydrolases, lyases, oxidoreductases and transferases, [1] these extracellular enzymes control soil enzyme activity through efficient degradation of biopolymers.

Contents

Plant residues, animals and microorganisms enter the dead organic matter pool upon senescence [3] and become a source of nutrients and energy for other organisms. Extracellular enzymes target macromolecules such as carbohydrates (cellulases), lignin (oxidases), organic phosphates (phosphatases), amino sugar polymers (chitinases) and proteins (proteases) [4] and break them down into soluble sugars that are subsequently transported into cells to support heterotrophic metabolism. [1]

Biopolymers are structurally complex and require the combined actions of a community of diverse microorganisms and their secreted exoenzymes to depolymerize the polysaccharides into easily assimilable monomers. These microbial communities are ubiquitous in nature, inhabiting both terrestrial and aquatic ecosystems. The cycling of elements from dead organic matter by heterotrophic soil microorganisms is essential for nutrient turnover and energy transfer in terrestrial ecosystems. [5] Exoenzymes also aid digestion in the guts of ruminants, [6] termites, [7] humans and herbivores. By hydrolyzing plant cell wall polymers, microbes release energy that has the potential to be used by humans as biofuel. [8] Other human uses include waste water treatment, [9] composting [10] and bioethanol production. [11]

Factors influencing extracellular enzyme activity

Extracellular enzyme production supplements the direct uptake of nutrients by microorganisms and is linked to nutrient availability and environmental conditions. The varied chemical structure of organic matter requires a suite of extracellular enzymes to access the carbon and nutrients embedded in detritus. Microorganisms differ in their ability to break down these different substrates and few organisms have the potential to degrade all the available plant cell wall materials. [12] To detect the presence of complex polymers, some exoenzymes are produced constitutively at low levels, and expression is upregulated when the substrate is abundant. [13] This sensitivity to the presence of varying concentrations of substrate allows fungi to respond dynamically to the changing availability of specific resources. Benefits of exoenzyme production can also be lost after secretion because the enzymes are liable to denature, degrade or diffuse away from the producer cell.

Enzyme production and secretion is an energy intensive process [14] and, because it consumes resources otherwise available for reproduction, there is evolutionary pressure to conserve those resources by limiting production. [15] Thus, while most microorganisms can assimilate simple monomers, degradation of polymers is specialized, and few organisms can degrade recalcitrant polymers like cellulose and lignin. [16] Each microbial species carries specific combinations of genes for extracellular enzymes and is adapted to degrade specific substrates. [12] In addition, the expression of genes that encode for enzymes is typically regulated by the availability of a given substrate. For example, presence of a low-molecular weight soluble substrate such as glucose will inhibit enzyme production by repressing the transcription of associated cellulose-degrading enzymes. [17]

Environmental conditions such as soil pH, [18] soil temperature, [19] moisture content, [20] and plant litter type and quality [21] have the potential to alter exoenzyme expression and activity. Variations in seasonal temperatures can shift metabolic needs of microorganisms in synchrony with shifts in plant nutrient requirements. [22] Agricultural practices such as fertilizer amendments and tillage can change the spatial distribution of resources, resulting in altered exoenzyme activity in the soil profile. [23] Introduction of moisture exposes soil organic matter to enzyme catalysis [24] and also increases loss of soluble monomers via diffusion. Additionally, osmotic shock resulting from water potential changes can impact enzyme activities as microbes redirect energy from enzyme production to synthesizing osmolytes to maintain cellular structures.

Extracellular enzyme activity in fungi during plant decomposition

Plant cell showing primary and secondary wall by CarolineDahl Plant cell showing primary and secondary wall by CarolineDahl.jpg
Plant cell showing primary and secondary wall by CarolineDahl

Most of the extracellular enzymes involved in polymer degradation in leaf litter and soil have been ascribed to fungi. [25] [26] [27] By adapting their metabolism to the availability of varying amounts of carbon and nitrogen in the environment, fungi produce a mixture of oxidative and hydrolytic enzymes to efficiently break down lignocelluloses like wood. During plant litter degradation, cellulose and other labile substrates are degraded first [28] followed by lignin depolymerization with increased oxidative enzyme activity and shifts in microbial community composition.

In plant cell walls, cellulose and hemicellulose is embedded in a pectin scaffold [29] that requires pectin degrading enzymes, such as polygalacturonases and pectin lyases to weaken the plant cell wall and uncover hemicellulose and cellulose to further enzymatic degradation. [30] Degradation of lignin is catalyzed by enzymes that oxidase aromatic compounds, such as phenol oxidases, peroxidases and laccases. Many fungi have multiple genes encoding lignin-degrading exoenzymes. [31]

Most efficient wood degraders are saprotrophic ascomycetes and basidiomycetes. Traditionally, these fungi are classified as brown rot (Ascomycota and Basidiomycota), white rot (Basidiomycota) and soft rot (Ascomycota) based on the appearance of the decaying material. [2] Brown rot fungi preferentially attack cellulose and hemicellulose; [32] while white rot fungi degrade cellulose and lignin. To degrade cellulose, basidiomycetes employ hydrolytic enzymes, such as endoglucanases, cellobiohydrolase and β-glucosidase. [33] Production of endoglucanases is widely distributed among fungi and cellobiohydrolases have been isolated in multiple white-rot fungi and in plant pathogens. [33] β-glucosidases are secreted by many wood-rotting fungi, both white and brown rot fungi, mycorrhizal fungi [34] and in plant pathogens. In addition to cellulose, β-glucosidases can cleave xylose, mannose and galactose. [35]

In white-rot fungi such as Phanerochaete chrysosporium , expression of manganese-peroxidase is induced by the presence of manganese, hydrogen peroxide and lignin, [36] while laccase is induced by availability of phenolic compounds. [37] Production of lignin-peroxidase and manganese-peroxidase is the hallmark of basidiomycetes and is often used to assess basidiomycete activity, especially in biotechnology applications. [38] Most white-rot species also produce laccase, a copper-containing enzyme that degrades polymeric lignin and humic substances. [39]

Brown-rot basidiomycetes are most commonly found in coniferous forests, and are so named because they degrade wood to leave a brown residue that crumbles easily. Preferentially attacking hemicellulose in wood, followed by cellulose, these fungi leave lignin largely untouched. [40] The decayed wood of soft-rot Ascomycetes is brown and soft. One soft-rot Ascomycete, Trichoderma reesei , is used extensively in industrial applications as a source for cellulases and hemicellulases. [41] Laccase activity has been documented in T. reesei, in some species in the Aspergillus genus [42] and in freshwater ascomycetes. [43]

Measuring fungal extracellular enzyme activity in soil, plant litter, and other environmental samples

Electronic PH meter Electronic PH meter.JPG
Electronic PH meter

Methods for estimating soil enzyme activities involve sample harvesting prior to analysis, mixing of samples with buffers and the use of substrate. Results can be influenced by: sample transport from field-site, storage methods, pH conditions for assay, substrate concentrations, temperature at which the assay is run, sample mixing and preparation. [44]

For hydrolytic enzymes, colorimetric assays are required that use a p-nitrophenol (p-NP)-linked substrate, [45] or fluorometric assays that use a 4-methylumbelliferone (MUF)-linked substrate. [46]

Oxidative enzymes such as phenol oxidase and peroxidase mediate lignin degradation and humification. [47] Phenol oxidase activity is quantified by oxidation of L-3, 4-dihydoxyphenylalanine (L-DOPA), pyrogallol (1, 2, 3-trihydroxybenzene), or ABTS (2, 2’-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid). Peroxidase activity is measured by running the phenol oxidase assay concurrently with another assay with L-DOPA and hydrogen peroxide (H2O2) added to every sample. [48] The difference in measurements between the two assays is indicative of peroxidase activity. Enzyme assays typically apply proxies that reveal exo-acting activities of enzymes. Exo-acting enzymes hydrolyze substrates from the terminal position. While activity of endo-acting enzymes which break down polymers midchain need to be represented by other substrate proxies. New enzyme assays aim to capture the diversity of enzymes and assess the potential activity of them in a more clear way. [49] [50] [51]

With newer technologies available, molecular methods to quantify abundance of enzyme-coding genes are used to link enzymes with their producers in soil environments. [52] [53] Transcriptome analyses are now employed to examine genetic controls of enzyme expression, [54] while proteomic methods can reveal the presence of enzymes in the environment and link to the organisms producing them. [55]

ProcessEnzymeSubstrate
Cellulose-degradationCellobiohydrolase

β-glucosidase

pNP, MUF [33] [56]
Hemicellulose-degradationβ-glucosidases

Esterases

pNP, MUF [57] [58]
Polysaccharide-degradationα-glucosidases

N-acetylglucosaminidase

pNP, MUF [59]
Lignin-degradationMn-peroxidase

Laccase (polyphenol oxidase)

Peroxidase

Pyrogallol, L-DOPA, ABTS [38]

L-DOPA, ABTS [39]

Applications of fungal extracellular enzymes

ApplicationEnzymes & their uses
Paper productionCellulases – improve paper quality and smooth fibers [60]

Laccases – soften paper and improving bleaching [61]

Biofuel generationCellulases – for production of renewable liquid fuels [62]
Dairy industryLactase – part of β-glucosidase family of enzymes and can break down lactose to glucose and galactose

Pectinases – in the manufacture of yogurt

Brewing industry
Black Sheep Brewery Tour Black Sheep Brewery Tour.jpg
Black Sheep Brewery Tour
Beer production and malting [63]
Fruit and jam manufacturing

Jelly Jars - Tanglewood Gardens - Nova Scotia, Canada.jpg

Pectinases, cellulases – to clarify fruit juices and form jams
Bioremediation Laccases – as biotransformers to remove nonionic surfactants [64] [65]
Waste water treatmentPeroxidases - removal of pollutants by precipitation [66] [67]
Sludge treatment Lipases - used in degradation of particulate organic matter [68]
Phytopathogen managementHydrolytic enzymes produced by fungi, e.g. Fusarium graminearum, pathogen on cereal grains resulting in economic losses in agriculture [69]
Resource management

Water retention

Soil aggregates and water infiltration influence enzyme activity [70] [71]
Soil fertility and plant productionUse of enzyme activity as indicator of soil quality [71] [72]
Composting

Drums with septic tank sludge with different amounts of urea added (6881892839).jpg

Impacts of composting municipal solid waste on soil microbial activity [10]
Soil organic matter stabilityImpact of temperature and soil respiration on enzymatic activity and its effect on soil fertility [73]
Climate change indicators

Impact on soil processes

Potential increase in enzymatic activity leading to elevated CO2 emissions [74]
Quantifying global warming outcomesPredictions based on soil organic matter decomposition [75] and strategies for mitigation [76]
Impact of elevated CO2 on enzyme activity & decompositionUnderstanding the implication of microbial responses and its impact on terrestrial ecosystem functioning [77]

See also

Related Research Articles

<span class="mw-page-title-main">Humus</span> Organic matter in soils resulting from decay of plant and animal materials

In classical soil science, humus is the dark organic matter in soil that is formed by the decomposition of plant and animal matter. It is a kind of soil organic matter. It is rich in nutrients and retains moisture in the soil. Humus is the Latin word for "earth" or "ground".

<span class="mw-page-title-main">Lignin</span> Structural phenolic polymer in plant cell walls

Lignin is a class of complex organic polymers that form key structural materials in the support tissues of most plants. Lignins are particularly important in the formation of cell walls, especially in wood and bark, because they lend rigidity and do not rot easily. Chemically, lignins are polymers made by cross-linking phenolic precursors.

<span class="mw-page-title-main">Polyporales</span> Order of fungi

The Polyporales are an order of about 1800 species of fungi in the division Basidiomycota. The order includes some polypores as well as many corticioid fungi and a few agarics. Many species within the order are saprotrophic, most of them wood-rotters. Some genera, such as Ganoderma and Fomes, contain species that attack living tissues and then continue to degrade the wood of their dead hosts. Those of economic importance include several important pathogens of trees and a few species that cause damage by rotting structural timber. Some of the Polyporales are commercially cultivated and marketed for use as food items or in traditional Chinese medicine.

<span class="mw-page-title-main">Exoenzyme</span> Exoenzyme

An exoenzyme, or extracellular enzyme, is an enzyme that is secreted by a cell and functions outside that cell. Exoenzymes are produced by both prokaryotic and eukaryotic cells and have been shown to be a crucial component of many biological processes. Most often these enzymes are involved in the breakdown of larger macromolecules. The breakdown of these larger macromolecules is critical for allowing their constituents to pass through the cell membrane and enter into the cell. For humans and other complex organisms, this process is best characterized by the digestive system which breaks down solid food via exoenzymes. The small molecules, generated by the exoenzyme activity, enter into cells and are utilized for various cellular functions. Bacteria and fungi also produce exoenzymes to digest nutrients in their environment, and these organisms can be used to conduct laboratory assays to identify the presence and function of such exoenzymes. Some pathogenic species also use exoenzymes as virulence factors to assist in the spread of these disease-causing microorganisms. In addition to the integral roles in biological systems, different classes of microbial exoenzymes have been used by humans since pre-historic times for such diverse purposes as food production, biofuels, textile production and in the paper industry. Another important role that microbial exoenzymes serve is in the natural ecology and bioremediation of terrestrial and marine environments.

<span class="mw-page-title-main">ABTS</span> Chemical compound

In biochemistry, ABTS is a chemical compound used to observe the reaction kinetics of specific enzymes. A common use for it is in the enzyme-linked immunosorbent assay (ELISA) to detect the binding of molecules to each other.

<span class="mw-page-title-main">Mycoremediation</span> Process of using fungi to degrade or sequester contaminants in the environment

Mycoremediation is a form of bioremediation in which fungi-based remediation methods are used to decontaminate the environment. Fungi have been proven to be a cheap, effective and environmentally sound way for removing a wide array of contaminants from damaged environments or wastewater. These contaminants include heavy metals, organic pollutants, textile dyes, leather tanning chemicals and wastewater, petroleum fuels, polycyclic aromatic hydrocarbons, pharmaceuticals and personal care products, pesticides and herbicides in land, fresh water, and marine environments.

Laccases are multicopper oxidases found in plants, fungi, and bacteria. Laccases oxidize a variety of phenolic substrates, performing one-electron oxidations, leading to crosslinking. For example, laccases play a role in the formation of lignin by promoting the oxidative coupling of monolignols, a family of naturally occurring phenols. Other laccases, such as those produced by the fungus Pleurotus ostreatus, play a role in the degradation of lignin, and can therefore be classed as lignin-modifying enzymes. Other laccases produced by fungi can facilitate the biosynthesis of melanin pigments. Laccases catalyze ring cleavage of aromatic compounds.

Lignin-modifying enzymes (LMEs) are various types of enzymes produced by fungi and bacteria that catalyze the breakdown of lignin, a biopolymer commonly found in the cell walls of plants. The terms ligninases and lignases are older names for the same class, but the name "lignin-modifying enzymes" is now preferred, given that these enzymes are not hydrolytic but rather oxidative by their enzymatic mechanisms. LMEs include peroxidases, such as lignin peroxidase, manganese peroxidase, versatile peroxidase, and many phenoloxidases of the laccase type.

<span class="mw-page-title-main">Wood-decay fungus</span> Any species of fungus that digests moist wood, causing it to rot

A wood-decay or xylophagous fungus is any species of fungus that digests moist wood, causing it to rot. Some species of wood-decay fungi attack dead wood, such as brown rot, and some, such as Armillaria, are parasitic and colonize living trees. Excessive moisture above the fibre saturation point in wood is required for fungal colonization and proliferation. In nature, this process causes the breakdown of complex molecules and leads to the return of nutrients to the soil. Wood-decay fungi consume wood in various ways; for example, some attack the carbohydrates in wood, and some others decay lignin. The rate of decay of wooden materials in various climates can be estimated by empirical models.

<i>Coriolopsis gallica</i> Species of fungus

Coriolopsis gallica is a fungus found growing on decaying wood. It is not associated with any plant disease, therefore it is not considered pathogenic. For various Coriolopsis gallica strains isolated, it has been found, as a common feature of the division Basidiomycota, that they are able to degrade wood components, mainly lignin and to lesser extent cellulose, which results in a degradation area covered by the accumulating -white- cellulose powder. Therefore, C. gallica might generically be called, as with many other basidiomycetes, a "white-rot" fungus.

In enzymology, a lignin peroxidase (EC 1.11.1.14) is an enzyme that catalyzes the chemical reaction

In enzymology, a manganese peroxidase (EC 1.11.1.13) is an enzyme that catalyzes the chemical reaction

<i>Cyathus stercoreus</i> Species of fungus

Cyathus stercoreus, commonly known as the dung-loving bird's nest or the dung bird's nest, is a species of fungus in the genus Cyathus, family Nidulariaceae. Like other species in the Nidulariaceae, the fruiting bodies of C. stercoreus resemble tiny bird's nests filled with eggs. The fruiting bodies are referred to as splash cups, because they are developed to use the force of falling drops of water to dislodge and disperse their spores. The species has a worldwide distribution, and prefers growing on dung, or soil containing dung; the specific epithet is derived from the Latin word stercorarius, meaning "of dung".

Versatile peroxidase (EC 1.11.1.16, VP, hybrid peroxidase, polyvalent peroxidase) is an enzyme with systematic name reactive-black-5:hydrogen-peroxide oxidoreductase. This enzyme catalyses the following chemical reaction

Myceliophthora thermophila is an ascomycete fungus that grows optimally at 45–50 °C (113–122 °F). It efficiently degrades cellulose and is of interest in the production of biofuels. The genome has recently been sequenced, revealing the full range of enzymes used by this organism for the degradation of plant cell wall material.

<span class="mw-page-title-main">Plastisphere</span> Plastic debris suspended in water and organisms which live in it

The plastisphere consists of ecosystems that have evolved to live in human-made plastic environments. All plastic accumulated in marine ecosystems serves as a habitat for various types of microorganisms, with the most notable contaminant being microplastics. There are an estimate of about 51 trillion microplastics floating in the oceans. Relating to the plastisphere, over 1,000 different species of microbes are able to inhabit just one of these 5mm pieces of plastic.

Priming or a "priming effect" is said to occur when something that is added to soil or compost affects the rate of decomposition occurring on the soil organic matter (SOM), either positively or negatively. Organic matter is made up mostly of carbon and nitrogen, so adding a substrate containing certain ratios of these nutrients to soil may affect the microbes that are mineralizing SOM. Fertilizers, plant litter, detritus, and carbohydrate exudates from living roots, can potentially positively or negatively prime SOM decomposition.

A mycoparasite is an organism with the ability to parasitize fungi.

Saprotrophic bacteria are bacteria that are typically soil-dwelling and utilize saprotrophic nutrition as their primary energy source. They are often associated with soil fungi that also use saprotrophic nutrition and both are classified as saprotrophs.

<i>Hypsizygus ulmarius</i> Species of mushroom-forming fungus

Hypsizygus ulmarius, also known as the elm oyster mushroom, and less commonly as the elm leech, elm Pleurotus, is an edible fungus. It has often been confused with oyster mushrooms in the Pleurotus genus but can be differentiated easily as the gills are either not decurrent or not deeply decurrent. While not quite as common as true oyster mushrooms, they have a wide range globally in temperate forests. The mushrooms and vegetative hyphae of this species have been studied in recent years for their potential benefits to human health, and mycoremediation.

References

  1. 1 2 3 Sinsabaugh, R. S. (1994). "Enzymic analysis of microbial pattern and process". Biology and Fertility of Soils. 17 (1): 69–74. doi:10.1007/BF00418675. ISSN   0178-2762. S2CID   20188510.
  2. 1 2 Burns, Richard G.; DeForest, Jared L.; Marxsen, Jürgen; Sinsabaugh, Robert L.; Stromberger, Mary E.; Wallenstein, Matthew D.; Weintraub, Michael N.; Zoppini, Annamaria (2013). "Soil enzymes in a changing environment: Current knowledge and future directions". Soil Biology and Biochemistry. 58: 216–234. doi:10.1016/j.soilbio.2012.11.009. ISSN   0038-0717.
  3. Cebrian, Just (1999). "Patterns in the Fate of Production in Plant Communities". The American Naturalist. 154 (4): 449–468. doi:10.1086/303244. ISSN   0003-0147. PMID   10523491. S2CID   4384243.
  4. Allison, S.D.; et al. (2007). "Soil enzymes: linking proteomics and ecological processes". In Hurst, CJ.; Crawford, RL.; Garland, JL.; Lipson DA.; Mills, AL; Stetzenbach, LD (eds.). Manual of environmental microbiology (3rd ed.). Washington, DC: ASM. pp. 704–711. ISBN   978-1-55581-379-6.
  5. Gessner, Mark O.; Swan, Christopher M.; Dang, Christian K.; McKie, Brendan G.; Bardgett, Richard D.; Wall, Diana H.; Hättenschwiler, Stephan (2010). "Diversity meets decomposition". Trends in Ecology & Evolution. 25 (6): 372–380. doi:10.1016/j.tree.2010.01.010. ISSN   0169-5347. PMID   20189677.
  6. Krause, Denis O; Denman, Stuart E; Mackie, Roderick I; Morrison, Mark; Rae, Ann L; Attwood, Graeme T; McSweeney, Christopher S (2003). "Opportunities to improve fiber degradation in the rumen: microbiology, ecology, and genomics". FEMS Microbiology Reviews. 27 (5): 663–693. doi: 10.1016/S0168-6445(03)00072-X . ISSN   0168-6445. PMID   14638418.
  7. Warnecke, F; et al. (2007). "Metagenomic and functional analysis of hindgut microbiota of a wood-feeding higher termite" (PDF). Nature. 450 (7169): 560–565. Bibcode:2007Natur.450..560W. doi:10.1038/nature06269. PMID   18033299. S2CID   4420494.
  8. Ragauskas, A. J. (2006). "The Path Forward for Biofuels and Biomaterials". Science. 311 (5760): 484–489. Bibcode:2006Sci...311..484R. doi:10.1126/science.1114736. ISSN   0036-8075. PMID   16439654. S2CID   9213544.
  9. Shackle, V.; Freeman, C.; Reynolds, B. (2006). "Exogenous enzyme supplements to promote treatment efficiency in constructed wetlands". Science of the Total Environment. 361 (1–3): 18–24. Bibcode:2006ScTEn.361...18S. doi:10.1016/j.scitotenv.2005.09.032. ISSN   0048-9697. PMID   16213577.
  10. 1 2 Crecchio, Carmine; Curci, Magda; Pizzigallo, Maria D.R.; Ricciuti, Patrizia; Ruggiero, Pacifico (2004). "Effects of municipal solid waste compost amendments on soil enzyme activities and bacterial genetic diversity". Soil Biology and Biochemistry. 36 (10): 1595–1605. doi:10.1016/j.soilbio.2004.07.016. ISSN   0038-0717.
  11. Wackett, Lawrence P (2008). "Biomass to fuels via microbial transformations". Current Opinion in Chemical Biology. 12 (2): 187–193. doi:10.1016/j.cbpa.2008.01.025. ISSN   1367-5931. PMID   18275861.
  12. 1 2 Allison, Steven D.; LeBauer, David S.; Ofrecio, M. Rosario; Reyes, Randy; Ta, Anh-Minh; Tran, Tri M. (2009). "Low levels of nitrogen addition stimulate decomposition by boreal forest fungi". Soil Biology and Biochemistry. 41 (2): 293–302. doi:10.1016/j.soilbio.2008.10.032. ISSN   0038-0717.
  13. Klonowska, Agnieszka; Gaudin, Christian; Fournel, André; Asso, Marcel; Le Petit, Jean; Giorgi, Michel; Tron, Thierry (2002). "Characterization of a low redox potential laccase from the basidiomycete C30". European Journal of Biochemistry. 269 (24): 6119–6125. doi: 10.1046/j.1432-1033.2002.03324.x . ISSN   0014-2956. PMID   12473107.
  14. Schimel, J (2003). "The implications of exoenzyme activity on microbial carbon and nitrogen limitation in soil: a theoretical model". Soil Biology and Biochemistry. 35 (4): 549–563. doi:10.1016/S0038-0717(03)00015-4. ISSN   0038-0717.
  15. Allison, Steven D.; Weintraub, Michael N.; Gartner, Tracy B.; Waldrop, Mark P. (2010). "Evolutionary-Economic Principles as Regulators of Soil Enzyme Production and Ecosystem Function". Soil Enzymology. Soil Biology. Vol. 22. pp. 229–243. CiteSeerX   10.1.1.689.2292 . doi:10.1007/978-3-642-14225-3_12. ISBN   978-3-642-14224-6. ISSN   1613-3382.
  16. Baldrian, Petr; Kolařík, Miroslav; Štursová, Martina; Kopecký, Jan; Valášková, Vendula; Větrovský, Tomáš; Žifčáková, Lucia; Šnajdr, Jaroslav; Rídl, Jakub; Vlček, Čestmír; Voříšková, Jana (2011). "Active and total microbial communities in forest soil are largely different and highly stratified during decomposition". The ISME Journal. 6 (2): 248–258. doi:10.1038/ismej.2011.95. ISSN   1751-7362. PMC   3260513 . PMID   21776033.
  17. Hanif, A (2004). "Induction, production, repression, and de-repression of exoglucanase synthesis in Aspergillus niger". Bioresource Technology. 94 (3): 311–319. doi:10.1016/j.biortech.2003.12.013. ISSN   0960-8524. PMID   15182839.
  18. DeForest, Jared L.; Smemo, Kurt A.; Burke, David J.; Elliott, Homer L.; Becker, Jane C. (2011). "Soil microbial responses to elevated phosphorus and pH in acidic temperate deciduous forests". Biogeochemistry. 109 (1–3): 189–202. doi:10.1007/s10533-011-9619-6. ISSN   0168-2563. S2CID   97965526.
  19. Wallenstein, Matthew D.; Haddix, Michelle L.; Lee, Daniel D.; Conant, Richard T.; Paul, Eldor A. (2012). "A litter-slurry technique elucidates the key role of enzyme production and microbial dynamics in temperature sensitivity of organic matter decomposition". Soil Biology and Biochemistry. 47: 18–26. doi:10.1016/j.soilbio.2011.12.009. ISSN   0038-0717.
  20. Fioretto, A.; Papa, S.; Curcio, E.; Sorrentino, G.; Fuggi, A. (2000). "Enzyme dynamics on decomposing leaf litter of Cistus incanus and Myrtus communis in a Mediterranean ecosystem". Soil Biology and Biochemistry. 32 (13): 1847–1855. doi:10.1016/S0038-0717(00)00158-9. ISSN   0038-0717.
  21. Waldrop, Mark P.; Zak, Donald R. (2006). "Response of Oxidative Enzyme Activities to Nitrogen Deposition Affects Soil Concentrations of Dissolved Organic Carbon". Ecosystems. 9 (6): 921–933. doi:10.1007/s10021-004-0149-0. ISSN   1432-9840. S2CID   10919578.
  22. Finzi, Adrien C; Austin, Amy T; Cleland, Elsa E; Frey, Serita D; Houlton, Benjamin Z; Wallenstein, Matthew D (2011). "Responses and feedbacks of coupled biogeochemical cycles to climate change: examples from terrestrial ecosystems". Frontiers in Ecology and the Environment. 9 (1): 61–67. doi:10.1890/100001. hdl: 11336/84335 . ISSN   1540-9295. S2CID   2862965.
  23. Poll, C.; Thiede, A.; Wermbter, N.; Sessitsch, A.; Kandeler, E. (2003). "Micro-scale distribution of microorganisms and microbial enzyme activities in a soil with long-term organic amendment". European Journal of Soil Science. 54 (4): 715–724. doi:10.1046/j.1351-0754.2003.0569.x. ISSN   1351-0754. S2CID   97005809.
  24. Fierer, N; Schimel, JP (2003). "A proposed mechanism for the pulse of carbon dioxide production commonly observed following the rapid rewetting of a dry soil". Soil Science Society of America Journal. 67 (3): 798–805. Bibcode:2003SSASJ..67..798F. doi:10.2136/sssaj2003.0798. S2CID   2815843.
  25. Boer, Wietse de; Folman, Larissa B.; Summerbell, Richard C.; Boddy, Lynne (2005). "Living in a fungal world: impact of fungi on soil bacterial niche development". FEMS Microbiology Reviews. 29 (4): 795–811. doi: 10.1016/j.femsre.2004.11.005 . ISSN   0168-6445. PMID   16102603.
  26. Hättenschwiler, Stephan; Tiunov, Alexei V.; Scheu, Stefan (2005). "Biodiversity and Litter Decomposition in Terrestrial Ecosystems". Annual Review of Ecology, Evolution, and Systematics. 36 (1): 191–218. doi:10.1146/annurev.ecolsys.36.112904.151932. ISSN   1543-592X.
  27. Baldrian, P (2009). "Microbial enzyme-catalyzed processes in soils and their analysis". Plant, Soil and Environment. 55 (9): 370–378. doi: 10.17221/134/2009-PSE .
  28. Berg, Björn (2000). "Litter decomposition and organic matter turnover in northern forest soils". Forest Ecology and Management. 133 (1–2): 13–22. doi:10.1016/S0378-1127(99)00294-7. ISSN   0378-1127.
  29. Ridley, Brent L; O'Neill, Malcolm A; Mohnen, Debra (2001). "Pectins: structure, biosynthesis, and oligogalacturonide-related signaling". Phytochemistry. 57 (6): 929–967. Bibcode:2001PChem..57..929R. doi:10.1016/S0031-9422(01)00113-3. ISSN   0031-9422. PMID   11423142.
  30. Lagaert, Stijn; Beliën, Tim; Volckaert, Guido (2009). "Plant cell walls: Protecting the barrier from degradation by microbial enzymes". Seminars in Cell & Developmental Biology. 20 (9): 1064–1073. doi:10.1016/j.semcdb.2009.05.008. ISSN   1084-9521. PMID   19497379.
  31. Courty, P. E.; Hoegger, P. J.; Kilaru, S.; Kohler, A.; Buée, M.; Garbaye, J.; Martin, F.; Kües, U. (2009). "Phylogenetic analysis, genomic organization, and expression analysis of multi-copper oxidases in the ectomycorrhizal basidiomyceteLaccaria bicolor". New Phytologist. 182 (3): 736–750. doi:10.1111/j.1469-8137.2009.02774.x. ISSN   0028-646X. PMID   19243515. S2CID   23324645.
  32. Martinez, AT; et al. (2005). "Biodegradation of lignocellulosics: microbial, chemical, and enzymatic aspects of the fungal attack of lignin". International Microbiology. 8 (3): 195–204. PMID   16200498.
  33. 1 2 3 Baldrian, Petr; Valášková, Vendula (2008). "Degradation of cellulose by basidiomycetous fungi". FEMS Microbiology Reviews. 32 (3): 501–521. doi: 10.1111/j.1574-6976.2008.00106.x . ISSN   0168-6445. PMID   18371173.
  34. Kusuda, Mizuho; Ueda, Mitsuhiro; Konishi, Yasuhito; Araki, Yoshihito; Yamanaka, Katsuji; Nakazawa, Masami; Miyatake, Kazutaka; Terashita, Takao (2006). "Detection of β-glucosidase as saprotrophic ability from an ectomycorrhizal mushroom, Tricholoma matsutake". Mycoscience. 47 (4): 184–189. doi:10.1007/s10267-005-0289-x. ISSN   1340-3540. S2CID   84906200.
  35. Valaskova, V.; Baldrian, P. (2006). "Degradation of cellulose and hemicelluloses by the brown rot fungus Piptoporus betulinus - production of extracellular enzymes and characterization of the major cellulases". Microbiology. 152 (12): 3613–3622. doi: 10.1099/mic.0.29149-0 . ISSN   1350-0872. PMID   17159214.
  36. Li D, Alic M, Brown JA, Gold MH (January 1995). "Regulation of manganese peroxidase gene transcription by hydrogen peroxide, chemical stress, and molecular oxygen". Appl. Environ. Microbiol. 61 (1): 341–5. Bibcode:1995ApEnM..61..341L. doi:10.1128/AEM.61.1.341-345.1995. PMC   167287 . PMID   7887613.
  37. Leonowicz, A; et al. (2001). "Fungal laccases: properties and activity on lignin". Journal of Basic Microbiology. 41 (3–4): 185–227. doi:10.1002/1521-4028(200107)41:3/4<185::aid-jobm185>3.0.co;2-t. PMID   11512451. S2CID   23523898.
  38. 1 2 Hofrichter, Martin (2002). "Review: lignin conversion by manganese peroxidase (MnP)". Enzyme and Microbial Technology. 30 (4): 454–466. doi:10.1016/S0141-0229(01)00528-2. ISSN   0141-0229.
  39. 1 2 Baldrian, Petr (2006). "Fungal laccases – occurrence and properties". FEMS Microbiology Reviews. 30 (2): 215–242. doi: 10.1111/j.1574-4976.2005.00010.x . ISSN   0168-6445. PMID   16472305.
  40. Hammel, Kenneth E.; Kapich, Alexander N.; Jensen, Kenneth A.; Ryan, Zachary C. (2002). "Reactive oxygen species as agents of wood decay by fungi". Enzyme and Microbial Technology. 30 (4): 445–453. doi:10.1016/S0141-0229(02)00011-X. ISSN   0141-0229. S2CID   96847091.
  41. Kumar, Raj; Singh, Sompal; Singh, Om V. (2008). "Bioconversion of lignocellulosic biomass: biochemical and molecular perspectives". Journal of Industrial Microbiology & Biotechnology. 35 (5): 377–391. doi: 10.1007/s10295-008-0327-8 . ISSN   1367-5435. PMID   18338189. S2CID   4830678.
  42. Tamayo-Ramos, Juan Antonio; van Berkel, Willem JH; de Graaff, Leo H (2012). "Biocatalytic potential of laccase-like multicopper oxidases from Aspergillus niger". Microbial Cell Factories. 11 (1): 165. doi: 10.1186/1475-2859-11-165 . ISSN   1475-2859. PMC   3548707 . PMID   23270588.
  43. Junghanns, C. (2005). "Degradation of the xenoestrogen nonylphenol by aquatic fungi and their laccases". Microbiology. 151 (1): 45–57. doi: 10.1099/mic.0.27431-0 . ISSN   1350-0872. PMID   15632424.
  44. German, Donovan P.; Weintraub, Michael N.; Grandy, A. Stuart; Lauber, Christian L.; Rinkes, Zachary L.; Allison, Steven D. (2011). "Optimization of hydrolytic and oxidative enzyme methods for ecosystem studies". Soil Biology and Biochemistry. 43 (7): 1387–1397. doi:10.1016/j.soilbio.2011.03.017. ISSN   0038-0717.
  45. Sinsabaugh, Robert L.; Linkins, Arthur E. (1990). "Enzymic and chemical analysis of particulate organic matter from a boreal river". Freshwater Biology. 23 (2): 301–309. doi:10.1111/j.1365-2427.1990.tb00273.x. ISSN   0046-5070.
  46. Marx, M.-C; Wood, M; Jarvis, S.C (2001). "A microplate fluorimetric assay for the study of enzyme diversity in soils". Soil Biology and Biochemistry. 33 (12–13): 1633–1640. doi:10.1016/S0038-0717(01)00079-7. ISSN   0038-0717.
  47. Sinsabaugh, Robert L. (2010). "Phenol oxidase, peroxidase and organic matter dynamics of soil". Soil Biology and Biochemistry. 42 (3): 391–404. doi:10.1016/j.soilbio.2009.10.014. ISSN   0038-0717.
  48. DeForest, Jared L. (2009). "The influence of time, storage temperature, and substrate age on potential soil enzyme activity in acidic forest soils using MUB-linked substrates and l-DOPA". Soil Biology and Biochemistry. 41 (6): 1180–1186. doi:10.1016/j.soilbio.2009.02.029. ISSN   0038-0717.
  49. Arnosti, C.; Bell, C.; Moorhead, D. L.; Sinsabaugh, R. L.; Steen, A. D.; Stromberger, M.; Wallenstein, M.; Weintraub, M. N. (January 2014). "Extracellular enzymes in terrestrial, freshwater, and marine environments: perspectives on system variability and common research needs". Biogeochemistry. 117 (1): 5–21. doi:10.1007/s10533-013-9906-5. ISSN   0168-2563. S2CID   83660222.
  50. Arnosti, Carol (2011-01-15). "Microbial Extracellular Enzymes and the Marine Carbon Cycle". Annual Review of Marine Science. 3 (1): 401–425. Bibcode:2011ARMS....3..401A. doi:10.1146/annurev-marine-120709-142731. ISSN   1941-1405. PMID   21329211.
  51. Obayashi, Y; Suzuki, S (2008-03-26). "Occurrence of exo- and endopeptidases in dissolved and particulate fractions of coastal seawater". Aquatic Microbial Ecology. 50: 231–237. doi: 10.3354/ame01169 . ISSN   0948-3055.
  52. Hassett, John E.; Zak, Donald R.; Blackwood, Christopher B.; Pregitzer, Kurt S. (2008). "Are Basidiomycete Laccase Gene Abundance and Composition Related to Reduced Lignolytic Activity Under Elevated Atmospheric NO3 − Deposition in a Northern Hardwood Forest?". Microbial Ecology. 57 (4): 728–739. doi:10.1007/s00248-008-9440-5. ISSN   0095-3628. PMID   18791762. S2CID   39272773.
  53. Lauber, Christian L.; Sinsabaugh, Robert L.; Zak, Donald R. (2008). "Laccase Gene Composition and Relative Abundance in Oak Forest Soil is not Affected by Short-Term Nitrogen Fertilization". Microbial Ecology. 57 (1): 50–57. doi:10.1007/s00248-008-9437-0. ISSN   0095-3628. PMID   18758844. S2CID   15755901.
  54. Morozova, Olena; Hirst, Martin; Marra, Marco A. (2009). "Applications of New Sequencing Technologies for Transcriptome Analysis". Annual Review of Genomics and Human Genetics. 10 (1): 135–151. doi:10.1146/annurev-genom-082908-145957. ISSN   1527-8204. PMID   19715439. S2CID   26713396.
  55. Wallenstein, Matthew D.; Weintraub, Michael N. (2008). "Emerging tools for measuring and modeling the in situ activity of soil extracellular enzymes". Soil Biology and Biochemistry. 40 (9): 2098–2106. doi:10.1016/j.soilbio.2008.01.024. ISSN   0038-0717.
  56. Lynd, L. R.; Weimer, P. J.; van Zyl, W. H.; Pretorius, I. S. (2002). "Microbial Cellulose Utilization: Fundamentals and Biotechnology". Microbiology and Molecular Biology Reviews. 66 (3): 506–577. doi:10.1128/MMBR.66.3.506-577.2002. ISSN   1092-2172. PMC   120791 . PMID   12209002.
  57. Collins, Tony; Gerday, Charles; Feller, Georges (2005). "Xylanases, xylanase families and extremophilic xylanases". FEMS Microbiology Reviews. 29 (1): 3–23. doi: 10.1016/j.femsre.2004.06.005 . ISSN   0168-6445. PMID   15652973.
  58. Biely, Peter; Puchart, Vladimír (2006). "Recent progress in the assays of xylanolytic enzymes". Journal of the Science of Food and Agriculture. 86 (11): 1636–1647. Bibcode:2006JSFA...86.1636B. doi:10.1002/jsfa.2519. ISSN   0022-5142.
  59. Seidl, Verena (2008). "Chitinases of filamentous fungi: a large group of diverse proteins with multiple physiological functions". Fungal Biology Reviews. 22 (1): 36–42. doi:10.1016/j.fbr.2008.03.002. ISSN   1749-4613.
  60. Ravalason, Holy; Jan, Gwénaël; Mollé, Daniel; Pasco, Maryvonne; Coutinho, Pedro M.; Lapierre, Catherine; Pollet, Brigitte; Bertaud, Frédérique; Petit-Conil, Michel; Grisel, Sacha; Sigoillot, Jean-Claude; Asther, Marcel; Herpoël-Gimbert, Isabelle (2008). "Secretome analysis of Phanerochaete chrysosporium strain CIRM-BRFM41 grown on softwood". Applied Microbiology and Biotechnology. 80 (4): 719–733. doi:10.1007/s00253-008-1596-x. ISSN   0175-7598. PMID   18654772. S2CID   24813930.
  61. Witayakran, Suteera; Ragauskas, Arthur J. (2009). "Modification of high-lignin softwood kraft pulp with laccase and amino acids". Enzyme and Microbial Technology. 44 (3): 176–181. doi:10.1016/j.enzmictec.2008.10.011. ISSN   0141-0229.
  62. Wilson, David B (2009). "Cellulases and biofuels". Current Opinion in Biotechnology. 20 (3): 295–299. doi:10.1016/j.copbio.2009.05.007. ISSN   0958-1669. PMID   19502046.
  63. Lalor, Eoin; Goode, Declan (2009). Brewing with Enzymes. pp. 163–194. doi:10.1002/9781444309935.ch8. ISBN   9781444309935.{{cite book}}: |journal= ignored (help)
  64. Martin, C.; Corvini, P. F. X.; Vinken, R.; Junghanns, C.; Krauss, G.; Schlosser, D. (2009). "Quantification of the Influence of Extracellular Laccase and Intracellular Reactions on the Isomer-Specific Biotransformation of the Xenoestrogen Technical Nonylphenol by the Aquatic Hyphomycete Clavariopsis aquatica". Applied and Environmental Microbiology. 75 (13): 4398–4409. Bibcode:2009ApEnM..75.4398M. doi:10.1128/AEM.00139-09. ISSN   0099-2240. PMC   2704831 . PMID   19429559.
  65. Strong, P. J.; Claus, H. (2011). "Laccase: A Review of Its Past and Its Future in Bioremediation". Critical Reviews in Environmental Science and Technology. 41 (4): 373–434. Bibcode:2011CREST..41..373S. doi:10.1080/10643380902945706. ISSN   1064-3389. S2CID   96397441.
  66. Durán, Nelson; Esposito, Elisa (2000). "Potential applications of oxidative enzymes and phenoloxidase-like compounds in wastewater and soil treatment: a review". Applied Catalysis B: Environmental. 28 (2): 83–99. doi:10.1016/S0926-3373(00)00168-5. ISSN   0926-3373.
  67. M., Kissi; M., Mountadar; O., Assobhei; E., Gargiulo; G., Palmieri; P., Giardina; G., Sannia (2001). "Roles of two white-rot basidiomycete fungi in decolorisation and detoxification of olive mill waste water". Applied Microbiology and Biotechnology. 57 (1–2): 221–226. doi:10.1007/s002530100712. ISSN   0175-7598. PMID   11693925. S2CID   1662318.
  68. Whiteley, C.G.; Burgess, J.E.; Melamane, X.; Pletschke, B.; Rose, P.D. (2003). "The enzymology of sludge solubilisation utilising sulphate-reducing systems: the properties of lipases". Water Research. 37 (2): 289–296. Bibcode:2003WatRe..37..289W. doi:10.1016/S0043-1354(02)00281-6. ISSN   0043-1354. PMID   12502058.
  69. Kikot, G.E.; et al. (2009). "Contributions of cell wall degrading enzymes to pathogenesis of Fusarium graminearum: a review". Journal of Basic Microbiology. 49 (3): 231–241. doi:10.1002/jobm.200800231. PMID   19025875. S2CID   45168988.
  70. Udawatta, Ranjith P.; Kremer, Robert J.; Garrett, Harold E.; Anderson, Stephen H. (2009). "Soil enzyme activities and physical properties in a watershed managed under agroforestry and row-crop systems". Agriculture, Ecosystems & Environment. 131 (1–2): 98–104. doi:10.1016/j.agee.2008.06.001. ISSN   0167-8809.
  71. 1 2 Powlson, D.S.; Gregory, P.J.; Whalley, W.R.; Quinton, J.N.; Hopkins, D.W.; Whitmore, A.P.; Hirsch, P.R.; Goulding, K.W.T. (2011). "Soil management in relation to sustainable agriculture and ecosystem services". Food Policy. 36: S72–S87. doi:10.1016/j.foodpol.2010.11.025. ISSN   0306-9192.
  72. Trasar-Cepeda, C.; Leirós, M.C.; Gil-Sotres, F. (2008). "Hydrolytic enzyme activities in agricultural and forest soils. Some implications for their use as indicators of soil quality". Soil Biology and Biochemistry. 40 (9): 2146–2155. doi:10.1016/j.soilbio.2008.03.015. hdl: 10261/49118 . ISSN   0038-0717.
  73. Jones, Chris D.; Cox, Peter; Huntingford, Chris (2003). "Uncertainty in climate-carbon-cycle projections associated with the sensitivity of soil respiration to temperature". Tellus B. 55 (2): 642–648. Bibcode:2003TellB..55..642J. doi:10.1034/j.1600-0889.2003.01440.x. ISSN   0280-6509.
  74. Kirschbaum, Miko U. F. (2004). "Soil respiration under prolonged soil warming: are rate reductions caused by acclimation or substrate loss?". Global Change Biology. 10 (11): 1870–1877. Bibcode:2004GCBio..10.1870K. doi:10.1111/j.1365-2486.2004.00852.x. ISSN   1354-1013. S2CID   86293310.
  75. Gillabel, Jeroen; Cebrian-Lopez, Beatriz; Six, Johan; Merckx, Roel (2010). "Experimental evidence for the attenuating effect of SOM protection on temperature sensitivity of SOM decomposition". Global Change Biology. 16 (10): 2789–2798. Bibcode:2010GCBio..16.2789G. doi:10.1111/j.1365-2486.2009.02132.x. ISSN   1354-1013. S2CID   86672269.
  76. Macías, Felipe; Camps Arbestain, Marta (2010). "Soil carbon sequestration in a changing global environment". Mitigation and Adaptation Strategies for Global Change. 15 (6): 511–529. doi:10.1007/s11027-010-9231-4. ISSN   1381-2386. S2CID   153406514.
  77. Zak, Donald R.; Pregitzer, Kurt S.; Burton, Andrew J.; Edwards, Ivan P.; Kellner, Harald (2011). "Microbial responses to a changing environment: implications for the future functioning of terrestrial ecosystems". Fungal Ecology. 4 (6): 386–395. doi:10.1016/j.funeco.2011.04.001. ISSN   1754-5048.

Further reading