Atomistic details of effect of disulfide bond reduction on active site of Phytase B from Aspergillus niger: A MD Study

The molecular integrity of the active site of phytases from fungi is critical for maintaining phytase function as efficient catalytic machines. In this study, the molecular dynamics (MD) of two monomers of phytase B from Aspergillus niger, the disulfide intact monomer (NAP) and a monomer with broken disulfide bonds (RAP), were simulated to explore the conformational basis of the loss of catalytic activity when disulfide bonds are broken. The simulations indicated that the overall secondary and tertiary structures of the two monomers were nearly identical but differed in some crucial secondary–structural elements in the vicinity of the disulfide bonds and catalytic site. Disulfide bonds stabilize the β-sheet that contains residue Arg66 of the active site and destabilize the α-helix that contains the catalytic residue Asp319. This stabilization and destabilization lead to changes in the shape of the active–site pocket. Functionally important hydrogen bonds and atomic fluctuations in the catalytic pocket change during the RAP simulation. None of the disulfide bonds are in or near the catalytic pocket but are most likely essential for maintaining the native conformation of the catalytic site.

Abbreviations

PhyB - 2.5 pH acid phophatese from Aspergillus niger, NAP - disulphide intact monomer of Phytase B, RAP - disulphide reduced monomer of Phytase B, Rg - radius of gyration, RMSD - root mean square deviation, MD - molecular dynamics.     

Enhancement of nitrogen release properties of urea–kaolinite fertilizer with chitosan binder

The use of controlled release fertilizer (CRF) has become a new trend to minimize environmental pollution. In this study, urea–kaolinite containing 20 wt% urea after one hour dry grinding was mixed with different concentrations of chitosan as a binder to prepare nitrogen-based CRF. Fourier transform infrared spectroscopy confirmed the hydrogen bonding between urea and kaolinite. Covalent interaction between urea–kaolinite and chitosan make the granules stronger. The nitrogen release was measured in 5 days interval using a diacetylmonoxime calorimetric method at a wavelength of 527 nm. The results illustrated that by increasing the chitosan concentration from 3 to 7.5%, nitrogen release decreased from 41.23 to 25.25% after one day and from 77.31 to 59.27% after 30 days incubation in water. Compressive stress at break tests confirmed that granules with chitosan 6% had the highest resistance and were chosen for ammonia volatilization tests. Ammonia volatilization was carried out using the forced-draft technique for a period of 10 weeks. The results showed that the total amount of ammonia loss for conventional urea fertilizer and urea–kaolinite–chitosan granules was 68.63 and 56.75%, respectively. This controlled release product could be applied in agricultural crop production purpose due to its controlled solubility in the soil, high nutrient use efficiency and potential economic benefits.     

厌氧氨氧化体的组成、结构与功能

厌氧氨氧化(Anammox)是微生物和环境领域的研究热点之一。厌氧氨氧化菌(AnAOB)是Anammox的功能载体。不同于大部分原核微生物,AnAOB具有独特的细胞器——厌氧氨氧化体,它是进行Anammox代谢的场所。研究厌氧氨氧化体有助于探明厌氧氨氧化菌的代谢特性。本文综述了厌氧氨氧化体的组成、结构与功能,以期为从事Anammox研究的同行提供参考。     

UV-B辐射对鲜土贝母中主要成分和抗氧化活性的影响

为探讨UV-B辐射对鲜土贝母有效成分和抗氧化活性的影响,对土贝母(Bolbostemma paniculatum)新鲜块茎的有效成分含量和抗氧化活性进行了研究。结果表明,100 k J m–2的高剂量UV-B辐射使鲜土贝母的还原糖含量升高60.17%,大黄素含量升高209.60%。辐射后还原能力及清除DPPH·自由基能力均显著高于对照(P0.01)。这说明UV-B辐射可显著提高土贝母鲜品的有效成分含量和抗氧化活性,因此鲜土贝母加工前进行UV-B辐射可望提高药材质量。     

Oxygen consumption and ammonia excretion of juvenile pink shrimp (Farfantepenaeus paulensis) in culture: temperature effects

We evaluated oxygen consumption and ammonia excretion by juveniles of the pink shrimp Farfantepenaeus paulensis at three different temperatures (15, 20 and 25 °C). The shrimp were collected in the coastal region of Cananéia, São Paulo State, Brazil. The selected temperatures are the limits recorded in aquaculture tanks in the coastal region of Cananéia. We measured oxygen consumption and ammonia excretion as proxies for metabolic activity. Oxygen consumption and ammonia excretion increased with increasing temperature, but no change was observed at 15 and 20 °C. It is possible that within this temperature range, there is thermal independence in juvenile F. paulensis do not need to allocate additional energy to compensate for temperature changes because they are physiologically adapted for this range.     

Global ammonia emissions from synthetic nitrogen fertilizer applications in agricultural systems: Empirical and process‐based estimates and uncertainty

Excessive ammonia (NH₃) emitted from nitrogen (N) fertilizer applications in global croplands plays an important role in atmospheric aerosol production, resulting in visibility reduction and regional haze. However, large uncertainty exists in the estimates of NH₃ emissions from global and regional croplands, which utilize different data and methods. In this study, we have coupled a process‐based Dynamic Land Ecosystem Model (DLEM) with the bidirectional NH₃ exchange module in the Community Multiscale Air‐Quality (CMAQ) model (DLEM‐Bi‐NH₃) to quantify NH₃ emissions at the global and regional scale, and crop‐specific NH₃ emissions globally at a spatial resolution of 0.5° × 0.5° during 1961–2010. Results indicate that global NH₃ emissions from N fertilizer use have increased from 1.9 ± 0.03 to 16.7 ± 0.5 Tg N/year between 1961 and 2010. The annual increase of NH₃ emissions shows large spatial variations across the global land surface. Southern Asia, including China and India, has accounted for more than 50% of total global NH₃ emissions since the 1980s, followed by North America and Europe. Rice cultivation has been the largest contributor to total global NH₃ emissions since the 1990s, followed by corn and wheat. In addition, results show that empirical methods without considering environmental factors (constant emission factor in the IPCC Tier 1 guideline) could underestimate NH₃ emissions in context of climate change, with the highest difference (i.e., 6.9 Tg N/year) occurring in 2010. This study provides a robust estimate on global and regional NH₃ emissions over the past 50 years, which offers a reference for assessing air quality consequences of future nitrogen enrichment as well as nitrogen use efficiency improvement.