Properties of protease-treated maize starches

Commercially produced maize starches were treated with protease (Promod 25P) and their composition and properties were compared with untreated controls. It was found that, although protease treatment reduced the starch protein contents by 41%, 21% and 37% for the waxy, normal and amylomaize starches, respectively, it also caused some pits on the granule surfaces, which were evident by scanning electron microscopy (SEM), but no obvious decrease in granule dimensions (Coulter Counter Multisizer). The protein extraction was associated with decreases in starch lipid content by 42%, 40% and 45% (waxy, normal and amylomaize starches, respectively) and a decrease in total amylose content (30.7–26.0%) for the normal maize starch. The gelatinisation parameters of the starches by differential scanning calorimetry (DSC) in water, 0.001 M HCl or NaOH were less obviously affected by protease treatment in common with the swelling factors at 80 °C. The amount of α-glucan leached by the swollen (80 °C) granules was, however, increased by the protease treatment by factors of 3.8, 1.4, and 1.1, for the waxy, normal and amylomaize starches, respectively. Although proteases provide a useful tool for the purification of native starches, commercial protease preparations need to be controlled in terms of amylase content to prevent modifications to starch structure and properties during industrial processing.     

蛋白酶对不同羊毛品种减量性能的研究

蛋白酶对不同羊毛品种将表现出不同的减量能力。在未经氧化预处理的情况下,Ｍａｘ－ａｃａｌＬ蛋白酶对各羊毛品种均有较大的减量能力,而其它蛋白酶减量能力却相对较小。在氧化预处理的情况下,蛋白酶对山羊毛的减量能力明显高于对其它羊毛品种的减量能力;蛋白酶对粗绒毛和细绒毛的减量能力也有所差异,对粗绒毛的减量能力略小于细绒毛,对国产羊毛的减量能力略小于澳州羊毛。在实际工艺处理过程中,为了保证处理质量,工艺处理参     

酸性蛋白酶抽提大米渣中蛋白质的研究

本文研究了从大米制饴糖后的米渣中提取蛋白质的条件，采用５３７酶在ｐＨ４及５０℃的条件下可有效地抽提大米蛋白，加酶量及加水量对抽提率有显著的影响。     

Engineering proteolytically-degradable artificial extracellular matrices

Hydrogels are widely used as provisional matrices for tissue engineering and regenerative medicine, showing also great promise as platforms for 3D cell culture. Different bio-functionalization strategies have been proposed to enhance the biological performance of hydrogels, particularly when they lack intrinsic bioactivity. In this context, the design of artificial materials that mimic structural and functional features of the natural extracellular matrix (ECM) has been pursued. This review presents an overview on bioengineering approaches of integrating protease-sensitive motifs into hydrogels, for the creation of cell-responsive biomimetic scaffolding materials that degrade in response to their proteolytic microenvironment. The successful incorporation of protease-sensitive motifs in several synthetic and natural polymers, which has been achieved using various chemical routes, is described. In each case, the selected peptide sequences and their target proteases are highlighted, along with the main achievements of the study. A critical analysis of current limitations and recent advances is also provided, along with suggestions for further improvements.     

毛霉产蛋白酶特性及条件研究

研究了毛霉产蛋白酶属性 ,毛霉的最适发酵方式 ,并采用正交试验确定了毛霉的培养基和培养条件。研究结果表明 :毛霉产蛋白酶以中性为主 ,毛霉更适合固体发酵培养 ,2 5 0ml三角瓶装入麸皮 10g ,加入 11ml水 ,按 8%的量接种菌悬液 ,30℃培养可使酶活达最高。     

Role of an autochthonous starter culture and the protease EPg222 on the sensory and safety properties of a traditional Iberian dry-fermented sausage "salchichón"

The effect of the addition of an autochthonous starter culture and the protease EPg222 on the physico-chemical and sensory characteristics of dry-fermented sausage ‘‘salchichon” was investigated. Sausages were prepared with purified EPg222 and Pediococcus acidilactici MS200 and Staphylococcus vitulus RS34 as starter culture (P200S34), separately and together, ripened for 90 days, and compared with a control batch. Dry-fermented sausages ripened with EPg222 and starter culture showed higher amounts of AN and volatile compounds derived from amino acid catabolism than the control, especially in samples in which was added the association of enzyme and starter culture (P200S34 + EPg222). There were clear differences shown by the texture analysis, with the P200S34 + EPg222 batch being less hard. Especially important was the result found in biogenic amines, since the association P200S34 + EPg222 reduced their accumulation compared to the EPg222 batch. The use of EPg222 may be of great interest to improve the sensory characteristics of dry-fermented sausages, but its association with the selected starter culture with low decarboxylase activity is necessary to guarantee healthiness and homogeneity.     

Purification of antioxidative peptides prepared from enzymatic hydrolysates of tuna dark muscle by-product

To produce and identify bioactive peptides, two commercial enzymes, orientase (OR) and protease XXIII (PR) were used to hydrolyze tuna dark muscle by-product for up to 6 h, and the hydrolysates were evaluated for antioxidative properties. The results showed that, 60-min OR and 120-min PR hydrolysates possessed the highest antioxidative activity. Then, the protein hydrolysates were subjected to a Sephadex G-25 gel filtration chromatography, and the molecular weight of the peptide fractions which showed the highest antioxidative activity ranged from 390 to 1400 Da. The peptide fractions were further isolated using the two-step high-performance liquid chromatography (HPLC-1 and HPLC-2), and the amino acid sequences of the two antioxidative peptides from OR and PR hydrolysates were Leu–Pro–Thr–Ser–Glu–Ala–Ala–Lys–Tyr (978 Da) and Pro–Met–Asp–Tyr–Met–Val–Thr (756 Da), respectively. We thus conclude that antioxidative hydrolysates from tuna dark muscle by-product may be useful ingredients in food and nutraceutical applications.     

Naturally fermented black olives: Effect on cell wall polysaccharides and on enzyme activities of Taggiasca and Conservolea varieties

Black olives of Taggiasca (Ta) and Conservolea (Co) varieties were processed according to the Greek style method in order to investigate the effect of this type of table olive processing on cell wall composition. Naturally black processing involves the storage in brine of fully ripe olives for several months, allowing a spontaneous fermentation by a mixed flora followed by fermentation by the lactic acid bacteria and yeasts. The smaller fruits of Ta variety are richer in pectic polysaccharides, accounting for half of total cell wall polysaccharides (12 mg/fruit), whereas in Co they accounted for one third (23 mg/fruit). Fresh Co olives had higher proportion of glucuronoxylans and xyloglucans (33%), whereas these polysaccharides accounted for 22% in Ta. The processing did not cause significant variations in the cell wall polysaccharide composition of Ta fruits, although pectic polysaccharides became more soluble in aqueous solutions. Conversely, processed Co olives had slightly higher amounts of galacturonan-rich pectic polysaccharides than the unprocessed fruits, suggesting that the long stage in brine might have contributed to the stabilisation and/or the biosynthesis of new polysaccharides. The changes caused by processing on cell wall polysaccharides appear to be closely related to the activity and availability of cell wall degrading enzymes.