A method for producing a debittered soybean protein concentrate

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  机译： 用转基因大豆生产改良大豆浓缩蛋白的方法

• 4. SOYBEAN PROTEIN CONCENTRATE WITH HIGH GEL STRENGTH AND METHOD FOR PRODUCING THE SAME [P] . 日本专利： JP2005287483A . 2005-10-20

  机译： 具有高凝胶强度的大豆浓缩蛋白及其制备方法

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  机译： 一种基于食品的浓缩物的制造方法，该浓缩物由植物蛋白，大豆，小麦，玉米，植物油和Inter Esterified配制而成，可选：与动物源蛋白混合

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• 1. Conformational and Functional Properties of Soybean Proteins Produced by Extrusion-Hydrolysis Approach [J] . Ma Wenjun ,Qi Baokun ,Rokayya Sami . 大豆科技 . 2019,第S01期
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• 4. BACKGROUND： Vibrio vulnifi cus inside the body could activate the NF-!B signaling pathwayand initiate the inflammatory cascade. The lung is one of the earliest organs affected by sepsisassociated with acute lung injury. High mobility group protein B1 （HMGB1） is an important late-actingpro-infl ammatory cytokine involving in the pathophysiology of sepsis. It is also involved in the injuryprocess in the lung, liver and intestine. There has been no report on the involvement of HMGB1 inVibrio vulnifi cus sepsis-induced lung injury.METHODS： Sixty rats were randomly divided into a normal control group （group A, n=10） anda Vibrio vulnificus sepsis group （group B, n=50）. Sepsis was induced in the rats by subcutaneousinjection of Vibrio vulnificus （concentration 6×108 cfu/mL, volume 0.1 mL/100g）） into the left lowerlimbs. The rats in group B were sacrifi ced separately 1, 6, 12, 24, and 48 hours after the infection.Their lungs were stored as specimens, lung water content was measured, and lung pathology wasobserved under a light microscope. The expressions of the HMGB1 gene and protein in the lungswere detected by RT-PCR and Western blot. Data were analyzed with one-way analysis of variance（ANOVA） and the LSD method for pair-wise comparison between the two groups. P〈0.05 wasconsidered statistically signifi cant.RESULTS： Compared to group A （0.652±0.177）, HMGB1 mRNA expression in the lungs ofgroup B was signifi cantly higher at 0 hour （1.161±0.358, P=0.013）, 24 hours （1.679±0.235, P=0.000）,and 48 hours （1.258±0.274, P=0.004） （P〈0.05）, and peaked at 24 hours. Compared to group A（0.594±0.190）, HMGB1 protein expression at 6 hours （1.408±0.567, P=0.026） after infection wassignificantly increased （P〈0. 05）, and peaked at 24 hours （2.415±1.064, P=0.000） after infection.Compared to group A （0.699±0.054）, lung water content was significantly increased at 6 hours（0.759±0.030, P=0.001）,12 hours （0.767±0.023, P=0.000）, 24 hours （0.771±0.043, P=0.000） and 48hours （0.789±0.137, P=0.000） after infection （P〈0.05）. Compared to group A, pathological changesat 12 hours in group B indicate marked pulmonary vascular congestion, interstitial edema andinfl ammatory infi ltration. Alveolar cavity collapse and boundaries of the alveolar septum could not beclearly identifi ed.CONCLUSION： Vibrio vulnifi cus sepsis can lead to injury in rat lungs, and increased HMGB1expression in lung tissue may be one of the mechanisms for injury from Vibrio vulnifi cus sepsis. [J] . Qiao-meng Qiu ,Zhong-wang Li ,Lu-ming Tang . 世界急诊医学杂志(英文) . 2011,第4期
• 5. 一种纯毛针织高捻单纱的生产方法 [C] . 周彩琴 ,陈娅琳 ,邹琛 . 全国织造新产品开发学术研讨会暨2017年织造年会 . 2017
• 6. 大豆蛋白的凝胶性与EDTAD改性大豆蛋白凝胶的制备与性能的研究 [A] . 王飞镝 . 2006