油脂脱臭馏出物富集VE的预处理研究概述

对脱臭馏出物的性状、组成及开发前景进行了介绍,重点对脱臭馏出物的甲酯化预处理特别是酶法预处理进行了阐述,最后列举了VE提取的实例。     

甲状腺素T4免疫传感器的研究

报道以甲基丙烯酸羟乙酯与甲基丙烯酸甲酯的共聚物为载体膜材料，研制成非酶标记的Ｔ４免疫传感器，并对载体膜材料的共聚方法及共聚物共聚比与传感器灵敏度的关系进行了探讨。     

氯丁橡胶的溶液接枝反应研究

本文研究了引发剂过氧化苯甲酰的用量对ＣＲ接技ＭＭＡ－ＡＡ反应的单体转化率、接枝率及接枝胶的粘度、剥离强度等的影响，并用红外光谱和元素和元素分析对反应产物进行了表征．结果表明，体系中存在接枝、降解、交联三种反应，在不同的配方和工艺条件下，三种反应的反应程度不同．     

Improvement of Coffee Aroma by Removal of Pungent Volatiles Using A-Type Zeolite

Experimental studies were conducted using molecular sieve zeolites to remove pungent smell components from a coffee aroma-containing gas evolved from roasted and ground coffee packed in a percolation vessel. The components such as methyl mercaptan or acetaldehyde were selectively adsorbed from coffee volatiles, and a decrease of pungent odor was recognized on sensory evaluation. The adsorption selectivity was based on pore sizes of adsorbents and molecular sizes of adsorbates. Zeolite 5Å was preferable to 4Å for separation efficiency of methyl mercaptan and recovery yield of residual volatile compounds.     

How Non-native Species in Lake Erie Influence Trophic Transfer of Mercury and Lead to Top Predators

Lake Erie's food web has been dramatically modified by exotic species. Both exotic dreissenid mussels and the round goby Neogobius melanastomus have shifted the food web from a pelagicbased to a benthic-based one, potentially creating a new pathway for contaminant transfer to top predators. Before the invasion of round gobies, few predators of dreissenids occurred in Lake Erie, allowing contaminants to be confined to these benthic organisms. The invasion of the round goby has produced a new pathway through which these contaminants can enter the food web. To characterize heavy-metal transfer through this new food web and to assess risk to humans, water, surficial sediment, dreissenid, round goby, and smallmouth bass Micropterus dolomieui samples were collected at three sites during summers, 2002 and 2003, and analyzed for total lead (Pb), total mercury (Hg), and methyl mercury (MeHg). In addition, we compared smallmouth bass Pb and Hg concentrations to those measured in 1993/1994, before round gobies were prevalent. Pb biodiminished and MeHg biomagnified through the food web to smallmouth bass; patterns were similar among our three sites. Total Pb concentrations in smallmouth bass were higher before the incorporation of round gobies into their diet. We attributed this decline to changes in food web structure, changes in contaminant burdens in prey, or declines in sediment Pb concentrations in Lake Erie. By comparison, Hg concentrations in smallmouth bass changed little, before and after the round goby invasion, possibly due to a shift in diet that increased growth. Despite a decline in sediment Hg concentrations in Lake Erie, smallmouth bass continued to accumulate Hg at historical rates possibly because of their high consumption rates of benthivorous round gobies. As smallmouth bass continue to consume round gobies during their lives, their Hg concentrations may well continue to increase, potentially increasing the risk of Hg contamination to humans.     

MCS接枝共聚物的结构和形态

将甲基丙烯酸甲酯（ＭＭＡ）、苯乙烯（Ｓ）在氯化聚乙烯（ＣＰＥ）存在下进行悬浮接枝共聚，获得ＭＣＳ树脂。本文着重考察了ＭＣＳ树脂的化学结构及胶粒形态。结果表明，确实发生了接枝共聚。ＣＰＥ用量、ＲＳＨ含量、引发剂浓度、反应温度、溶胀时间及聚合转化率对ＭＣＳ树脂的接枝率、接枝效率均有影响。ＭＣＳ树脂是接枝共聚物、ＭＭＡ／Ｓ共聚物与ＭＭＡ均聚物的混合物，橡胶相ＣＰＥ在ＭＣＳ树脂中的分散情况为“海岛结构”，     

Mn/Ti-Zr复合氧化物催化苯甲酸甲酯选择性加氢

以硝酸锆和钛酸四丁酯为原料,采用共沉淀法制备Ti-Zr-O氧化物载体,采用浸渍法制备了Mn/Ti-Zr催化剂;采用XRD、N2物理吸附、H2-TPR、NH3-TPD和TG-DTA对Mn/Ti-Zr催化剂进行了表征,并考察了催化剂组成、结构和反应条件对苯甲酸甲酯（MB）加氢性能的影响,以及催化剂的长周期稳定性、失活和再生行为。结果表明：TiO2含量和Mn负载量分别为12% 和8% （二者均以Ti-Zr-O氧化物的质量为基准,下同）时制备的Mn/Ti-Zr催化剂性能最优,该催化剂在θ = 390 ℃, p = 1.0 MPa,n(H2)∶n(MB) = 9∶1和重时空速（WHSV）= 0.5 h-1的优化条件能够实现98.0% 的苯甲酸甲酯转化率和89.7%的苯甲醛和苯甲醇选择性;苯甲酸甲酯加氢反应的活性和选择性分别与Mn/Ti-Zr表面MnOx物种的氧化还原性和催化剂的酸性密切相关。此外,Mn/Ti-Zr催化剂具有良好的结构稳定性,在反应1000 h后仅因积碳而丧失11% 的活性,且轻微失活的催化剂可以通过焙烧恢复其初始活性和选择性。     

An Engineered Biliverdin-Compatible Cyanobacteriochrome Enables a Unique Ultrafast Reversible Photoswitching Pathway

Cyanobacteriochromes (CBCRs) are promising optogenetic tools for their diverse absorption properties with a single compact cofactor-binding domain. We previously uncovered the ultrafast reversible photoswitching dynamics of a red/green photoreceptor AnPixJg2, which binds phycocyanobilin (PCB) that is unavailable in mammalian cells. Biliverdin (BV) is a mammalian cofactor with a similar structure to PCB but exhibits redder absorption. To improve the AnPixJg2 feasibility in mammalian applications, AnPixJg2_BV4 with only four mutations has been engineered to incorporate BV. Herein, we implemented femtosecond transient absorption (fs-TA) and ground state femtosecond stimulated Raman spectroscopy (GS-FSRS) to uncover transient electronic dynamics on molecular time scales and key structural motions responsible for the photoconversion of AnPixJg2_BV4 with PCB (Bpcb) and BV (Bbv) cofactors in comparison with the parent AnPixJg2 (Apcb). Bpcb adopts the same photoconversion scheme as Apcb, while BV4 mutations create a less bulky environment around the cofactor D ring that promotes a faster twist. The engineered Bbv employs a reversible clockwise/counterclockwise photoswitching that requires a two-step twist on ~5 and 35 picosecond (ps) time scales. The primary forward P_fr → P_o transition displays equal amplitude weights between the two processes before reaching a conical intersection. In contrast, the primary reverse P_o → P_fr transition shows a 2:1 weight ratio of the ~35 ps over 5 ps component, implying notable changes to the D-ring-twisting pathway. Moreover, we performed pre-resonance GS-FSRS and quantum calculations to identify the Bbv vibrational marker bands at ~659,797, and 1225 cm⁻¹. These modes reveal a stronger H-bonding network around the BV cofactor A ring with BV4 mutations, corroborating the D-ring-dominant reversible photoswitching pathway in the excited state. Implementation of BV4 mutations in other PCB-binding GAF domains like AnPixJg4, AM1_1870g3, and NpF2164g5 could promote similar efficient reversible photoswitching for more directional bioimaging and optogenetic applications, and inspire other bioengineering advances.     

A Methionine Chemical Shift Based Order Parameter Characterizing Global Protein Dynamics

Coupling of side chain dynamics over long distances is an important component of allostery. Methionine side chains show the largest intrinsic flexibility among methyl-containing residues but the actual degree of conformational averaging depends on the proximity and mobility of neighboring residues. The ¹³C NMR chemical shifts of the methyl groups of methionine residues located at long distances in the same protein show a similar scaling with respect to the values predicted from the static X-ray structure by quantum methods. This results in a good linear correlation between calculated and observed chemical shifts. The slope is protein dependent and ranges from zero for the highly flexible calmodulin to 0.7 for the much more rigid calcineurin catalytic domain. The linear correlation is indicative of a similar level of side-chain conformational averaging over long distances, and the slope of the correlation line can be interpreted as an order parameter of the global side-chain flexibility.