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This study was undertaken to find the optimum conditions of a new enzymatic process to remove plant residues from wool. Commercial enzymatic preparations of Celluclast 1.5 L and Pectinex Ultra SP-L were selected in order to hydrolyze the polysaccharides in primary plant cell walls and middle lamella, resulting into more fragile residues easier to be removed. Since it was intended to define the optimal conditions for enzyme application, a four-factor central composite design was selected to study the effects of pH, temperature, enzyme concentration and wetting agent concentration, on the two selected responses, i.e., soluble reducing sugars (RS) and alkali solubility (AS) of wool to detect plant degradation and to evaluate wool quality, respectively. Results demonstrated that enzyme concentration was the most significant effect in plant residues degradation. A total enzyme concentration loading of 20 mL of both diluted enzymatic preparations in equal parts per 1 L of incubation solution (42.970 U/L of Celluclast preparation and PG 29.3 nkat/L + PME 2.537 nkat/L of Pectinex preparation), yielded an equivalent amount of 240.127 mg of glucose per 1.0 g of plant residue, at the optimal conditions: 40.56 °C, pH 4.0 and 1 mL Plurafac/L. SEM analysis has indicated an identical and important degradation of the plant residues, when compared to the conventional carbonization process, and wool quality has been preserved.  相似文献   
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STIM1 is a MT-plus-end-tracking protein involved in remodeling of the ER   总被引:7,自引:0,他引:7  
Stromal interaction molecule 1 (STIM1) is a transmembrane protein that is essential for store-operated Ca(2+) entry, a process of extracellular Ca(2+) influx in response to the depletion of Ca(2+) stores in the endoplasmic reticulum (ER) (reviewed in [1-4]). STIM1 localizes predominantly to the ER; upon Ca(2+) release from the ER, STIM1 translocates to the ER-plasma membrane junctions and activates Ca(2+) channels (reviewed in [1-4]). Here, we show that STIM1 directly binds to the microtubule-plus-end-tracking protein EB1 and forms EB1-dependent comet-like accumulations at the sites where polymerizing microtubule ends come in contact with the ER network. Therefore, the previously observed tubulovesicular motility of GFP-STIM1 [5] is not a motor-based movement but a traveling wave of diffusion-dependent STIM1 concentration in the ER membrane. STIM1 overexpression strongly stimulates ER extension occurring through the microtubule "tip attachment complex" (TAC) mechanism [6, 7], a process whereby an ER tubule attaches to and elongates together with the EB1-positive end of a growing microtubule. Depletion of STIM1 and EB1 decreases TAC-dependent ER protrusion, indicating that microtubule growth-dependent concentration of STIM1 in the ER membrane plays a role in ER remodeling.  相似文献   
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The aim of our study was to assess the intraspecific variation of a range of leaf attributes and carbon isotope discrimination (Δ), in Quercus suber, along an 800 mm rainfall gradient in Portugal. We measured specific leaf area (SLA), leaf thickness (LT) and density, and used leaf carbon isotope content as an integrated record of water use efficiency. The values of SLA of Q. suber were strongly, positively correlated with rainfall, decreasing as rainfall decreased. This reduction was mainly driven by LT, which was tightly correlated with SLA (= −0.80, P < 0.001), and steadily increased with declining rainfall. The significant increase in carbon isotope discrimination towards the wetter end of the gradient, with a difference of 4.2‰ in Δ between the two extremes, suggests a strong adjustment of leaf gas exchange to water availability. Leaf changes associated with precipitation in Q. suber thus seem to influence water economy, since reduction of SLA with the increase of LT with aridity improves water use efficiency. These data suggest that this evergreen tree species relies on its foliage plasticity and physiology to overcome water shortage.  相似文献   
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