Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
Add more filters










Database
Language
Publication year range
1.
Sci Total Environ ; 625: 640-646, 2018 Jun 01.
Article in English | MEDLINE | ID: mdl-29304502

ABSTRACT

Nitrogen (N) availability affects litter decomposition and nutrient dynamics, especially in N-limited ecosystems. We investigated the response of litter decomposition to N additions in Eriophorum vaginatum and Vaccinium uliginosum peatlands. These two species dominate peatlands in Northeast China. In 2012, mesh bags containing senesced leaf litter of Eriophorum vaginatum and Vaccinium uliginosum were placed in N addition plots and sprayed monthly for two years with NH4NO3 solution at dose rates of 0, 6, 12, and 24gNm-2year-1 (CK, N1, N2 and N3, respectively). Mass loss, N and phosphorus (P) content, and enzymatic activity were measured over time as litter decomposed. In the control plots, V. uliginosum litter decomposed faster than E. vaginatum litter. N1, N2, and N3 treatments increased the mass losses of V. uliginosum litter by 6%, 9%, and 4% respectively, when compared with control. No significant influence of N additions was found on the decomposition of E. vaginatum litter. However, N and P content in E. vaginatum litter and V. uliginosum litter significantly increased with N additions. Moreover, N additions significantly promoted invertase and ß-glucosidase activity in E. vaginatum and V. uliginosum litter. However, only in V. uliginosum litter was polyphenol oxidase activity significantly enhanced. Our results showed that initial litter quality and polyphenol oxidase activity influence the response of plant litter to N additions in peatland ecosystems. Increased N availability may change peatland soil N and P cycling by enhancing N and P immobilization during litter decomposition.


Subject(s)
Cyperaceae/enzymology , Ecosystem , Nitrogen/chemistry , Soil/chemistry , Vaccinium/enzymology , China , Phosphorus/chemistry , Plant Leaves
2.
Pestic Biochem Physiol ; 135: 78-81, 2017 Jan.
Article in English | MEDLINE | ID: mdl-28043335

ABSTRACT

Cyperus difformis L. (CYPDI) and Schoenoplectus mucronatus (L.) Palla (SCHMU) are major weeds of California (CA) rice, where resistance to acetolactate synthase (ALS)-inhibitors was identified in several CYPDI and SCHMU populations that have also evolved resistance to photosystem II (PSII)-inhibiting herbicides. The mechanism of ALS resistance in these populations remains to be clarified but this information is crucial in a weed management program, especially in a scenario where resistance to multiple herbicides has been identified. ALS activity assays are commonly used to diagnose resistance to ALS-inhibitors, but protocols currently available are burdensome for the study of CYPDI and SCHMU, as they require large amounts of plant material from young seedlings and have low yields. Our objective was to investigate the ALS resistance mechanism in suspected ALS-resistant (R) CYPDI and SCHMU biotypes using a modified ALS activity assay that requires less plant material. ALS enzymes from suspected R biotypes were at least 10,000-fold less sensitive to bensulfuron-methyl than susceptible (S) cohorts, indicating ALS resistance that is likely due to an altered target-site. Protein concentration (mgg-1 tissue) did not differ between R and S biotypes within each species, suggesting that R biotypes do not over produce ALS enzymes. CYPDI biotypes had up to 4-fold more protein per mg of tissue than SCHMU biotypes, but up to 7-fold more acetoin per mg-1 protein was quantified in SCHMU, suggesting greater ALS catalytic ability in SCHMU biotypes, regardless of their herbicide resistance status. Our optimized protocol to measure ALS activity allowed for up to a 3-fold increase in the number of assays performed per g of leaf tissue. The modified assay may be useful for measuring ALS activity in other weed species that also produce small amount of foliage in early growth stages when protein in tissue is most abundant.


Subject(s)
Acetolactate Synthase/metabolism , Cyperaceae/drug effects , Herbicides/toxicity , Plant Proteins/metabolism , Seedlings/drug effects , Sulfonylurea Compounds/toxicity , Biological Assay , Cyperaceae/enzymology , Herbicide Resistance , Plant Weeds/drug effects , Plant Weeds/enzymology , Seedlings/enzymology
3.
Environ Pollut ; 158(10): 3157-63, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20674110

ABSTRACT

Here we investigate the response of soils and litter to 5 years of experimental additions of ammonium (NH4), nitrate (NO3), and ammonia (NH3) to an ombrotrophic peatland. We test the importance of direct (via soil) and indirect (via litter) effects on phosphatase activity and efflux of CO2. We also determined how species representing different functional types responded to the nitrogen treatments. Our results demonstrate that additions of NO3, NH4 and NH3 all stimulated phosphatase activity but the effects were dependent on species of litter and mechanism (direct or indirect). Deposition of NH3 had no effect on efflux of CO2 from Calluna vulgaris litter, despite it showing signs of stress in the field, whereas both NO3 and NH4 reduced CO2 fluxes. Our results show that the collective impacts on peatlands of the three principal forms of nitrogen in atmospheric deposition are a result of differential effects and mechanisms on individual components.


Subject(s)
Ammonia/chemistry , Carbon/analysis , Nitrates/chemistry , Nitrates/toxicity , Phosphoric Monoester Hydrolases/metabolism , Quaternary Ammonium Compounds/chemistry , Ammonia/metabolism , Ammonia/toxicity , Calluna/drug effects , Calluna/enzymology , Calluna/metabolism , Carbon/chemistry , Carbon/metabolism , Carbon Cycle , Cyperaceae/drug effects , Cyperaceae/enzymology , Cyperaceae/metabolism , Ecosystem , Environmental Monitoring , Nitrates/metabolism , Phosphoric Monoester Hydrolases/chemistry , Quaternary Ammonium Compounds/metabolism , Quaternary Ammonium Compounds/toxicity , Soil Pollutants/chemistry , Soil Pollutants/metabolism , Soil Pollutants/toxicity , Sphagnopsida/drug effects , Sphagnopsida/metabolism
4.
Mol Biol Evol ; 26(8): 1909-19, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19461115

ABSTRACT

C(4) photosynthesis is an adaptive trait conferring an advantage in warm and open habitats. It originated multiple times and is currently reported in 18 plant families. It has been recently shown that phosphoenolpyruvate carboxylase (PEPC), a key enzyme of the C(4) pathway, evolved through numerous independent but convergent genetic changes in grasses (Poaceae). To compare the genetics of multiple C(4) origins on a broader scale, we reconstructed the evolutionary history of the C(4) pathway in sedges (Cyperaceae), the second most species-rich C(4) family. A sedge phylogeny based on two plastome genes (rbcL and ndhF) has previously identified six fully C(4) clades. Here, a relaxed molecular clock was used to calibrate this tree and showed that the first C(4) acquisition occurred in this family between 19.6 and 10.1 Ma. According to analyses of PEPC-encoding genes (ppc), at least five distinct C(4) origins are present in sedges. Two C(4) Eleocharis species, which were unrelated in the plastid phylogeny, acquired their C(4)-specific PEPC genes from a single source, probably through reticulate evolution or a horizontal transfer event. Acquisitions of C(4) PEPC in sedges have been driven by positive selection on at least 16 codons (3.5% of the studied gene segment). These sites underwent parallel genetic changes across the five sedge C(4) origins. Five of these sites underwent identical changes also in grass and eudicot C(4) lineages, indicating that genetic convergence is most important within families but that identical genetic changes occurred even among distantly related taxa. These lines of evidence give new insights into the constraints that govern molecular evolution.


Subject(s)
Biological Evolution , Cyperaceae/genetics , Photosynthesis , Cyperaceae/enzymology , Cyperaceae/physiology , Phosphoenolpyruvate Carboxylase/genetics , Phylogeny , Selection, Genetic
5.
J Agric Food Chem ; 57(10): 4273-8, 2009 May 27.
Article in English | MEDLINE | ID: mdl-19385656

ABSTRACT

Two biotypes of Scirpus mucronatus not controlled with the herbicide bensulfuron-methyl in rice fields were characterized by using field, greenhouse, and laboratory techniques. Seeds were collected in two rice areas [Parral (R1) and Linares (R2)], where bensulfuron-methyl at 150 g ha(-1) did not control S. mucronatus. A third seed sample of S. mucronatus susceptible (S) to bensulfuron-methyl was collected in an area from Chile. The dose-response studies confirmed resistance to bensulfuron-methyl in R1 and R2 S. mucronatus biotypes; ratios (R/S) of the ED(50) values of resistant to susceptible plants were 1719 and 1627 for R1 and R2, respectively. The biotype R1 also showed strong cross-resistance (ratios ranging from 1719 to 43) to sulfonylureas (bensulfuron-methyl, cyclosulfamuron, ethoxysulfuron, imazosulfuron, and pyrazosulfuron-ethyl) and imidazolinone (imazamox) and a weak cross-resistance (ratio of 1.705) to pyrimidinyloxybenzoates (bispyribac-sodium), all ALS inhibiting herbicides used in rice. Absorption, translocation, and metabolism results did not explain the differences in susceptibility among biotypes. The in vitro assays confirmed cross-resistance to all ALS inhibitors tested and the level of cross resistance was bensulfuron-methyl > imazosulfuron ≫ cyclosulfamuron ≫ pyrazosulfuron-ethyl ≫ ethoxysulfuron > imazamox ≫ bispiribac-sodium. Molecular studies demonstrated that the Pro197His amino acid substitution on the ALS enzyme could explain the loss of affinity for the ALS-inhibiting herbicides.


Subject(s)
Cyperaceae/drug effects , Herbicide Resistance , Oryza/growth & development , Sulfonylurea Compounds/pharmacology , Acetolactate Synthase/antagonists & inhibitors , Acetolactate Synthase/chemistry , Amino Acid Sequence , Chile , Cyperaceae/enzymology , Cyperaceae/genetics , Enzyme Inhibitors/pharmacology , Seeds/drug effects
6.
Mol Biol Evol ; 25(11): 2361-8, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18695049

ABSTRACT

Rubisco is responsible for the fixation of CO2 into organic compounds through photosynthesis and thus has a great agronomic importance. It is well established that this enzyme suffers from a slow catalysis, and its low specificity results into photorespiration, which is considered as an energy waste for the plant. However, natural variations exist, and some Rubisco lineages, such as in C4 plants, exhibit higher catalytic efficiencies coupled to lower specificities. These C4 kinetics could have evolved as an adaptation to the higher CO2 concentration present in C4 photosynthetic cells. In this study, using phylogenetic analyses on a large data set of C3 and C4 monocots, we showed that the rbcL gene, which encodes the large subunit of Rubisco, evolved under positive selection in independent C4 lineages. This confirms that selective pressures on Rubisco have been switched in C4 plants by the high CO2 environment prevailing in their photosynthetic cells. Eight rbcL codons evolving under positive selection in C4 clades were involved in parallel changes among the 23 independent monocot C4 lineages included in this study. These amino acids are potentially responsible for the C4 kinetics, and their identification opens new roads for human-directed Rubisco engineering. The introgression of C4-like high-efficiency Rubisco would strongly enhance C3 crop yields in the future CO2-enriched atmosphere.


Subject(s)
Cyperaceae/genetics , Photosynthesis/genetics , Plant Proteins/genetics , Poaceae/genetics , Ribulose-Bisphosphate Carboxylase/genetics , Adaptation, Biological , Biotechnology , Carbon Dioxide/metabolism , Codon , Crops, Agricultural/enzymology , Crops, Agricultural/genetics , Cyperaceae/classification , Cyperaceae/enzymology , Evolution, Molecular , Phylogeny , Poaceae/classification , Poaceae/enzymology , Selection, Genetic
7.
Chembiochem ; 9(13): 2096-103, 2008 Sep 01.
Article in English | MEDLINE | ID: mdl-18666307

ABSTRACT

Drug discovery often begins with the screening of large compound libraries to identify lead compounds. Recently, the enzymes that are involved in the biosynthesis of natural products have been investigated for their potential to generate new, diverse compound libraries. There have been several approaches toward this end, including altering the substrate specificities of the enzymes involved in natural product biosynthesis and engineering functional communication between enzymes from different biosynthetic pathways. While there exist assays to assess the substrate specificity of enzymes involved in these pathways, there is no simple method for determining whether enzymes from different synthases will function cooperatively to generate the desired product(s). Herein we report a method that provides insight into both substrate specificity and compatibility of protein-protein interactions between the acyl carrier protein (ACP) and ketosynthase (KS) domains involved in fatty acid and polyketide biosynthesis. Our technique uses a one-pot chemoenzymatic method to generate post-translationally modified ACPs that are capable of covalently interacting with KS domains from different biosynthetic systems. The extent of interaction between ACPs and KSs from different systems is easily detected and quantified by a gel-based method. Our results are consistent with previous studies of substrate specificity and ACP-KS binding interactions and provide new insight into unnatural substrate and protein interactions.


Subject(s)
Cyperaceae/enzymology , Escherichia coli/enzymology , Fatty Acid Synthase, Type II/chemistry , Fatty Acid Synthase, Type II/metabolism , Polyketide Synthases/chemistry , Polyketide Synthases/metabolism , Amino Acid Sequence , Cross-Linking Reagents/chemical synthesis , Cross-Linking Reagents/chemistry , Cross-Linking Reagents/pharmacology , Drug Design , Molecular Sequence Data , Pantetheine/analogs & derivatives , Pantetheine/chemical synthesis , Pantetheine/chemistry , Pantetheine/pharmacology , Protein Binding , Protein Structure, Tertiary , Substrate Specificity
8.
New Phytol ; 170(3): 491-500, 2006.
Article in English | MEDLINE | ID: mdl-16626471

ABSTRACT

Caustis blakei produces an intriguing morphological adaptation by inducing dauciform roots in response to phosphorus (P) deficiency. We tested the hypothesis that these hairy, swollen lateral roots play a similar role to cluster roots in the exudation of organic chelators and ectoenzymes known to aid the chemical mobilization of sparingly available soil nutrients, such as P. Dauciform-root development and exudate composition (carboxylates and acid phosphatase activity) were analysed in C. blakei plants grown in nutrient solution under P-starved conditions. The distribution of dauciform roots in the field was determined in relation to soil profile depth and matrix. The percentage of dauciform roots of the entire root mass was greatest at the lowest P concentration ([P]) in solution, and was suppressed with increasing solution [P], while in the field dauciform roots were predominantely located in the upper soil horizons, and decreased with increasing soil depth. Citrate was the major carboxylate released in an exudative burst from mature dauciform roots, which also produced elevated levels of acid phosphatase activity. Malonate was the dominant internal carboxylate present, with the highest concentration in young dauciform roots. The high concentration of carboxylates and phosphatases released from dauciform roots, combined with their prolific distribution in the organic surface layer of nutrient-impoverished soils, provides an ecophysiological advantage for enhancing nutrient acquisition.


Subject(s)
Acid Phosphatase/metabolism , Carboxylic Acids/metabolism , Cyperaceae/growth & development , Cyperaceae/metabolism , Phosphorus/physiology , Plant Roots/growth & development , Plant Roots/metabolism , Cyperaceae/enzymology , Phosphorus/deficiency , Plant Roots/anatomy & histology , Soil/analysis
SELECTION OF CITATIONS
SEARCH DETAIL
...