Role of Phosphatase Enzymes in Soil
By P. Nannipieri, L. Giagnoni, L. Landi, G. Renella. 2011
878 citations recorded by the source corpus.
Subfields: Plant Science, Pollution, Soil Science
View Paper: https://www.semanticscholar.org/paper/8e603d0e481ade3debe100145cf394a1f91f3b39
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Citations in the corpus
- Distribution of phosphatase activity and various bacterial phyla in the rhizosphere of Hordeum vulgare L. depending on P availability (2015, background): “…92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 both acid and alkaline phosphatases, plants only can produce acid phosphatases (Dick et al., 1983; Juma and Tabatabai, 1988; Nannipieri et al., 2011).”
- Soil bacterial phoD gene abundance and expression in response to applied phosphorus and long-term management (2015, background): “This lack of response may be explained bymeasurement of activity in the assay beyond that induced under P starvation, such as activity from phosphatases stabilized on soil particles or constitutively released by microbial cells (Nannipieri et al., 2011).”
- Rhizosphere priming: a nutrient perspective (2013, background): “The P in these bonds can be released by hydrolysis with the help of phosphatase enzymes (without causing CO2 production, Nannipieri et al., 2011), rather than through oxidation of organic matter (causing CO2 production).”
- Distribution of microbial- and root-derived phosphatase activities in the rhizosphere depending on P availability and C allocation – Coupling soil zymography with 14C imaging (2013, background): “While microbes are capable of producing both acid and alkaline phosphatases, plants only can produce acid phosphatases (Dick et al., 1983; Juma and Tabatabai, 1988; Nannipieri et al., 2011).”
- Long-term fertilisation regimes affect the composition of the alkaline phosphomonoesterase encoding microbial community of a vertisol and its derivative soil fractions (2017, background): “Soil ALP activity was significantly affected by the different long-term fertilisation regimes, being increased by the addition of organic matter as already reported (Saha et al. 2008; Sakurai et al. 2008; Nannipieri et al. 2011; Zhang et al. 2014a), but decreased by the addition of mineral P (Saha e”
- Stability and dynamics of enzyme activity patterns in the rice rhizosphere: Effects of plant growth and temperature (2017, background): “Such an increase is mainly connected to the production of this common enzyme by both plants and microorganisms (Blagodatskaya and Kuzyakov, 2008; Dick and Tabatabai, 1984; Nannipieri et al., 2011).”
- Tricalcium phosphate is inappropriate as a universal selection factor for isolating and testing phosphate-solubilizing bacteria that enhance plant growth: a proposal for an alternative procedure (2013, background): “Enzymatically driven dissolution of phosphate may be an essential process in organic phosphorus-rich soils, involving phosphatase-driven hydrolysis of poorly soluble organic phosphate esters, which release inorganic phosphate (Rodriguez et al. 2006; Nannipieri et al. 2011).”
- Stoichiometric responses of soil microflora to nutrient additions for two temperate forest soils (2017, background): “Nannipieri et al. (2011, 2012) reported that application of inorganic P could repress AP synthesis in soils.”
- Decreased soil organic P fraction associated with ectomycorrhizal fungal activity to meet increased P demand under N application in a subtropical forest ecosystem (2017, background): “Generally, ACP activity was higher at low inorganic P content of soil than at high content (Nannipieri et al. 2011), which might be because increased inorganic P can repress the synthesis of phosphomonoesterases in soil because it inhibits the expression of PHO genes (Oshima et al. 1996).”
- Phosphate solubilizing microbes: sustainable approach for managing phosphorus deficiency in agricultural soils (2013, background): “Among the variety of phosphatase enzyme classes released by PSM, phosphomonoesterases (often just called phosphatases) are the most abundant and best studied (Nannipieri et al. 2011).”
- Quantification of bacterial non-specific acid (phoC) and alkaline (phoD) phosphatase genes in bulk and rhizosphere soil from organically managed soybean fields (2017, background): “, 2015; Tarafdar and Claassen,1998) has been well documented, production of ALK has been primarily reported from soil bacteria and some fungi (Nannipieri et al., 2011).”