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1.
Environ Monit Assess ; 196(8): 717, 2024 Jul 09.
Article in English | MEDLINE | ID: mdl-38980472

ABSTRACT

Traditional ecological knowledge (TEK) possessed by indigenous communities offers a vital source of information regarding the status and threats faced by species. Anaphalis javanica (DC.) Sch.Bip. commonly known as Javanese edelweiss is a culturally significant species in Indonesia's mountainous regions, yet conservation efforts for it remain limited. We utilized TEK to assess the status and threats to the Javanese edelweiss in Bromo Tengger Semeru National Park, Indonesia. The research aims to assess the distribution, abundance, population trends, and threats faced by Javanese edelweiss using TEK. We interviewed 641 individuals from seven Tengger villages near the park to gather data on the distribution, status, and threats facing the Javanese edelweiss, contributing to conservation efforts. Data were analyzed using generalized linear mixed models and ordinal logistic regression. TEK regarding the Javanese edelweiss was extensive, as 96.3% of respondents recognized the plant. A majority (73.2%) had observed Javanese edelweiss in the wild, yet a significant portion (85%) perceived it as "very rare" or "rare." Furthermore, 50% of respondents reported a decline in its population. Variations in sighting frequency, perceived abundance, and population trends across different locations provide crucial insights for identifying priority areas and shaping community-based conservation strategies for Javanese edelweiss. This research underscores the importance of integrating TEK into conservation planning, emphasizing community involvement for effective and sustainable biodiversity conservation.


Subject(s)
Conservation of Natural Resources , Parks, Recreational , Indonesia , Humans , Asteraceae , Environmental Monitoring/methods , Knowledge , Ecology
2.
Vet World ; 14(1): 11-22, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33642781

ABSTRACT

BACKGROUND AND AIM: Flushing with the manipulation of fatty acids, particularly polyunsaturated fatty acids, like linoleic and α-linolenic acids in the ration, is a strategy to raise the nutritional status of the female mammals to improve ovarian function and follicle development. This study was designed to investigate the effectiveness of flushing supplementation with different types of polyunsaturated and saturated fatty acids in stimulating follicle growth and development during estrus in Ettawa Grade does with a low initial body condition score (BCS ≤2). MATERIALS AND METHODS: Eighteen Ettawa Grade does in the second parity, with an average body weight of 32.11±2.19 kg, were divided into three groups according to the fatty acid supplemented to their ration: (i) About 2.8% lauric acid flushing (group); (ii) 2.8% linoleic acid flushing (LA group); and (iii) 2.8% α-linolenic acid flushing (ALA group). The ration was formulated to be isocaloric (total digestible nutrient = 77%) and isonitrogenous (crude protein = 15%). The experiment was conducted for 35 days; that is, 14 days for acclimatization and synchronization of the estrous cycle and 21 days for fatty acid flushing until the appearance of the next estrus. A completely randomized design was applied. RESULTS: According to the results, none of the different fatty acids in the ration affected the nutrient intakes, BCSs, average daily gains, and plasma glucose, cholesterol, and progesterone concentrations of the three groups of does. However, the BCSs (by 0.8-0.9) and the plasma cholesterol concentrations were higher after fatty acid flushing for 21 days than before the flushing period. The ALA group had the highest number of large-sized preovulatory follicles, whereas the LAURIC group had the highest plasma estradiol concentration during estrus. All three groups had similar plasma progesterone concentrations during estrus after fatty acid flushing. CONCLUSION: Flushing supplementation with 2.8% ALA from flaxseed oil gave the best results in terms of stimulating the highest number of large-sized preovulatory follicles in Ettawa Grade does.

3.
Anal Bioanal Chem ; 405(7): 2371-7, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23307126

ABSTRACT

It is estimated that up to 50% of the adult population take antioxidant products on a daily basis to promote their health status. Strangely, despite the well-recognized importance of antioxidants, currently there is no international standard index for labeling owing to the lack of standardized methods for antioxidant measurement in complex products. Here, an online high-performance liquid chromatography (HPLC)-based method to detect and measure the total antioxidant capacity of antioxidant samples is presented. In this approach, complex samples containing antioxidants are separated by the HPLC system, which is further coupled to an antioxidant measuring system consisting of an optical oxygen sensor, laccase, and tetramethoxy azobismethylene quinone (TMAMQ). The antioxidants, separated via HPLC, reduce TMAMQ to syringaldazine, which is then reoxidized by laccase while simultaneously consuming O(2). The amount of consumed oxygen is directly proportional to the concentration of antioxidants and is measured by the optical oxygen sensor. The sensor is fabricated by coating a glass capillary with an oxygen-sensitive thin layer made of platinum(II) meso-tetra(4-fluorophenyl)tetrabenzoporphyrin and polystyrene, which makes real-time analysis possible (t(90) = 1.1 s in solution). Four selected antioxidants (3 mM), namely, catechin, ferulic acid, naringenin (used as a control), and Trolox, representing flavonol, hydrocinnamic acid, flavanone, and vitamin E, respectively, were injected into the online antioxidant monitoring system, separated, and then mixed with the TMAMQ/laccase solution, which resulted in oxygen consumption. This study shows that, with the use of such a system, the antioxidant activity of individual antioxidant molecules in a sample and their contribution to the total antioxidant activity of the sample can be correctly assigned.


Subject(s)
Antioxidants/analysis , Biosensing Techniques/methods , Chromatography, High Pressure Liquid/methods , Fungal Proteins/chemistry , Laccase/chemistry , Oxygen/chemistry , Trametes/enzymology , Biosensing Techniques/instrumentation , Oxidation-Reduction , Trametes/chemistry
4.
Adv Biochem Eng Biotechnol ; 125: 47-68, 2011.
Article in English | MEDLINE | ID: mdl-21089004

ABSTRACT

Enzymatic polymer functionalisation has entered its most fascinating period with development in this field largely at the basic research level and pilot scale applications. Development of enzymatic processes for the development of lignocellulose-based functional polymers has not been spared, ranging from textile fibres with novel properties (antimicrobials properties, hydrophobic properties, attractive shed colours, etc.) to fibreboards. Enzymatic processes are also being actively pursued aimed at developing functional polymers from lignin (a major by product of the pulp and process).


Subject(s)
Biological Products/chemistry , Laccase/chemistry , Lignin/chemical synthesis , Peroxidase/chemistry , Wood/chemistry , Enzyme Activation , Enzyme Stability , Substrate Specificity
5.
Bioresour Technol ; 101(14): 5054-62, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20176477

ABSTRACT

The ability of laccases from Trametes villosa (TvL), Myceliophthora thermophila (MtL), Trametes hirsuta (ThL) and Bacillus subtilis (BsL) to improve the dispersion properties of calcium lignosulfonates 398 in the presence of HBT as a mediator was investigated. Size exclusion chromatography showed an extensive increase in molecular weight of the samples incubated with TvL and ThL by 107% and 572% from 28400 Da after 17h of incubation, respectively. Interestingly, FTIR spectroscopy, (13)C NMR and Py-GC/MS analysis of the treated samples suggested no substantial changes in the aromatic signal of the lignosulfonates, a good indication of the ability of TvL/ThL-HBT systems to limit their effect on functional groups without degrading the lignin backbone. Further, the enzymatic treatments led to a general increase in the dispersion properties, indeed a welcome development for its application in polymer blends.


Subject(s)
Biodegradation, Environmental , Laccase/chemistry , Lignin/analogs & derivatives , Triazoles/chemistry , Water Purification/methods , Bacillus subtilis/metabolism , Gas Chromatography-Mass Spectrometry/methods , Lignin/chemistry , Magnetic Resonance Spectroscopy , Molecular Weight , Photons , Polymers/chemistry , Spectroscopy, Fourier Transform Infrared/methods , Sulfones/chemistry , Time Factors
6.
Anal Bioanal Chem ; 393(2): 679-87, 2009 Jan.
Article in English | MEDLINE | ID: mdl-18958446

ABSTRACT

A novel antioxidant activity assay was developed using laccase-oxidized phenolics. In a three-step approach, phenolic compounds were first oxidized by laccase. Laccase was then inhibited using 80% (v/v) methanol which also stabilized the oxidized phenolics which were then used to measure antioxidant activities of ascorbic acid and Trolox. From a number of laccase-oxidized phenolics screened for potential use in the measurement of antioxidant activities, syringaldazine emerged the best, giving results comparable to the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical, which is currently used in conventional methods. Like DPPH radicals, two moles of stoichiometric oxidized syringaldazine were reduced by one mole of either ascorbic acid or Trolox. For the first time we show that antioxidant activity can be correlated to oxygen consumption by laccase. Reduction of one molecule of oxygen corresponded to oxidation of four molecules of syringaldazine which in turn is reduced by two molecules of Trolox or ascorbic acid. This study therefore demonstrates the great potential of using laccase-oxidized syringaldazine for the measurement of antioxidant activity.


Subject(s)
Antioxidants/analysis , Ascorbic Acid/analysis , Biological Assay/methods , Chromans/analysis , Laccase/metabolism , Picrates/metabolism , Antioxidants/metabolism , Ascorbic Acid/metabolism , Biphenyl Compounds , Chromans/metabolism , Free Radicals/chemistry , Free Radicals/metabolism , Laccase/antagonists & inhibitors , Methanol/pharmacology , Oxidation-Reduction , Oxygen/chemistry , Oxygen/metabolism , Phenols/chemistry , Phenols/metabolism , Picrates/chemistry , Spectrophotometry, Ultraviolet , Time Factors
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