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冬虫夏草原生质体制备与再生条件的研究 被引量:12
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作者 郭成金 赵润 《食品科学》 EI CAS CSCD 北大核心 2009年第5期166-170,共5页
采用正交分析方法,对影响冬虫夏草菌株原生质体制备与再生的主要因素进行研究。结果表明,最佳条件组合为培养3d的菌丝体,在2.0%溶壁酶+1.0%蜗牛酶的酶液中,0.6mol/L的KCl作为原生质体制备的渗稳剂,0.6mol/L的甘露醇作为再生培养基的渗稳... 采用正交分析方法,对影响冬虫夏草菌株原生质体制备与再生的主要因素进行研究。结果表明,最佳条件组合为培养3d的菌丝体,在2.0%溶壁酶+1.0%蜗牛酶的酶液中,0.6mol/L的KCl作为原生质体制备的渗稳剂,0.6mol/L的甘露醇作为再生培养基的渗稳剂,32℃酶解2h。在此条件下,原生质体得率可达到2.98×108/ml,再生率可达到42.09×10-2。 展开更多
关键词 冬虫夏草 正交分析 原生质体制备 再生
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番茄匍柄霉原生质体的制备与再生体系构建 被引量:1
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作者 龚伟杰 刘洪 +2 位作者 黄萍 王慧 周倩 《浙江农业学报》 CSCD 北大核心 2022年第2期337-342,共6页
以番茄匍柄霉(Stemphylium lycopersici)CS12菌株为研究对象,从菌龄、酶种类与浓度、酶组合、酶解温度与时间、不同渗透压稳定剂等方面对番茄匍柄霉原生质体制备条件进行了优化,并筛选了最适再生培养基,成功建立番茄匍柄霉原生质体制备... 以番茄匍柄霉(Stemphylium lycopersici)CS12菌株为研究对象,从菌龄、酶种类与浓度、酶组合、酶解温度与时间、不同渗透压稳定剂等方面对番茄匍柄霉原生质体制备条件进行了优化,并筛选了最适再生培养基,成功建立番茄匍柄霉原生质体制备与再生体系。番茄匍柄霉CS12在菌龄为36 h,稳渗剂为0.7 mol·L^(-1) NaCl溶液,酶解液为10 mg·mL^(-1) Kitalase裂解酶,28℃酶解3.5 h的条件下制备的原生质体效果好,在YEPS再生培养基上再生效率最高。番茄匍柄霉原生质体制备与再生体系的建立,为进一步研究番茄匍柄霉致病机理与功能基因组学奠定了基础。 展开更多
关键词 番茄匍柄霉 原生质体 再生 稳渗剂 菌龄
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The Effect of pH on the Permeation of Lidocaine Hydrochloride Across Excised Rat Skin
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作者 贾士聪 丁平田 +2 位作者 郑俊民 吴翠栓 华士元 《Journal of Chinese Pharmaceutical Sciences》 CAS 2001年第3期133-135,共3页
The effect of pH on the permeation of Lidocaine hydrochloride (LH) across excised rat skin was studied, the steady state flux (JSS) at different pH being determined using improved Valia-Chien diffusion cells. JSS incr... The effect of pH on the permeation of Lidocaine hydrochloride (LH) across excised rat skin was studied, the steady state flux (JSS) at different pH being determined using improved Valia-Chien diffusion cells. JSS increased substantially when pH was close to the pKa of LH. The profile of JSS versus pH showed an 慡?shaped curve. JSS of Lidocaine free base (LFB) was fourteen times that of LH. The pH of vehicle influences the permeation of LH significantly and should be considered as an important factor when a formulation is developed. 展开更多
关键词 PH PKA LIDOCAINE PERMEATION
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Optimization the Cell Wall Degrading Enzymes and Technique for Isolation of Protoplasts in Potato
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作者 Le Minh Phuong Hana Vodickova +1 位作者 Brigitazamecnikova Jaromir Lachman 《Journal of Pharmacy and Pharmacology》 2016年第4期179-182,共4页
Plasma membrane of plant cells is surrounded by cellulose wall and adjacent cells are joined together by a thick pectin rich matrix. Separation of plant cells and removal of the cell wall experimentally, by either a m... Plasma membrane of plant cells is surrounded by cellulose wall and adjacent cells are joined together by a thick pectin rich matrix. Separation of plant cells and removal of the cell wall experimentally, by either a mechanical or an enzymatic process, results in the production ofprotoplast. Protoplasts are useful tools to study the uptake and transport ofmacromolecules and production of somatic hybrids. Protoplasts can be obtained from all types of actively growing young and healthy tissues. The most convenient and widely used source of plant protoplasts is leaf. Juvenile seedling tissues, cotyledons are other alternative tissues most frequently used for protoplasts isolation. All the environmental and genotypic factors, which affect the cell wall thickenings and compactness indirectly, influence the number of protoplasts recovered. Protoplasts are isolated by two methods, mechanical and enzymatic. The enzyme mixture solution of celluiose/macerozyme is used to digest the cell wall. The critical factors affecting the obtaning ofprotoplasts are the kinds of cell wall degrading enzymes, the physiological state of plant leaves, the type of osmotic stabilizers and the composition of reaction solution. With the improvement of technique and enzyme combination rate, the yield of collected protoplasts will be increased higher. 展开更多
关键词 Plasma membrane PROTOPLAST enzyme cell wall potato plant.
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