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Nitrogen Sources Affect Streptolydigin Production and Related Secondary Metabolites Distribution of Streptomyces lydicus AS 4.2501 被引量:2
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作者 李良智 乔斌 元英进 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2007年第3期403-410,共8页
The effects of nitrogen sources on streptolydigin production and distribution of secondary metabolites were investigated for flask cultured S.lydicus AS 4.2501.When peptone,asparamide,and glutamic acid were ex- amined... The effects of nitrogen sources on streptolydigin production and distribution of secondary metabolites were investigated for flask cultured S.lydicus AS 4.2501.When peptone,asparamide,and glutamic acid were ex- amined as the nitrogen source,respectively,liquid chromatography-mass spectrometry(LC-MS)and photodiode array(PDA)analyses revealed the formation of two analogues of streptolydigin in the fermentation broth.When soybean meal was used as the source of nitrogen,three analogues of streptolydigin were detected.The use of am- monium sulfate as a source of nitrogen resulted in a lower pH value of the fermentation system,thus inhibiting streptolydigin biosynthesis and changing the metabolic profiling.Among the nitrogen sources that were made use of,glutamic acid was most favorable to the formation of streptolydigin.Simultaneously,this study also showed that the changing nitrogen sources resulted in altering the production and relative ratios of streptolydigin and its analogues. 展开更多
关键词 Streptomyces lydicus nitrogensource ANALOGUE secondary metabolite streptolydigin
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Effects of Propionate on Streptolydigin Production and Carbon Flux Distribution in Streptomyces lydicus AS 4.2501
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作者 李良智 郑卉 元英进 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2007年第2期143-149,共7页
To achieve higher antibiotic streptolydigin productivity through metabolic regulation, propionate was fed during the fermentation of Streptomyces lydicus AS 4.2501. The effects of propionate feeding on streptolydigin ... To achieve higher antibiotic streptolydigin productivity through metabolic regulation, propionate was fed during the fermentation of Streptomyces lydicus AS 4.2501. The effects of propionate feeding on streptolydigin production and intracellular fluxes were investigated. The highest streptolydigin production yield of 95.10mg·L-1 was obtained when 2mmol·L-1 of sodium propionate was added at 60h of cultivation into shake-flask culture. This yield is 23.06% higher when compared to that of a batch culture without propionate supplementation. It was also found that when propionate was added, much more organic acids were excreted. Metabolic flux analysis was per-formed and it demonstrated that the carbon fluxes of the pentose phosphate pathway and the anaplerotic reaction were significantly increased after propionate feeding. The carbon flux from pyruvate to acetyl-CoA was determined to be 24.7, which was 12.27% higher than that in the batch culture. This study indicated that the glu-cose-6-phosphate and pyruvate nodes were potential bottlenecks for increasing streptolydigin productivity. Potential targets and strategies that could be manipulated through genetic and process engineering to increase the production of streptolydigin were also suggested. 展开更多
关键词 streptolydigin PROPIONATE FEEDING metabolic flux Streptomyces lydicus antibiotic
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代谢物组分析利迪链菌素生物合成代谢转变
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作者 李良智 李小林 咸漠 《化学与生物工程》 CAS 2008年第11期39-43,共5页
为进一步明确利迪链菌素生物合成时从初级代谢到次级代谢的转变,运用ESI-MS和PCA分析,对利迪链霉菌AS 4.2501生产利迪链菌素不同发酵阶段的细胞内外代谢物进行代谢物组研究。结果表明,利用代谢物组学的方法能区分开不同发酵阶段的代谢产... 为进一步明确利迪链菌素生物合成时从初级代谢到次级代谢的转变,运用ESI-MS和PCA分析,对利迪链霉菌AS 4.2501生产利迪链菌素不同发酵阶段的细胞内外代谢物进行代谢物组研究。结果表明,利用代谢物组学的方法能区分开不同发酵阶段的代谢产物,特别是根据第三主成分(PC3)可明显将细胞进入次级代谢与初级代谢阶段区分开,结合文献和MS/MS分析,推断代谢转变过程的生物标志物主要源于磷脂和蛋白类化合物。 展开更多
关键词 代谢物组 利迪链菌素 代谢转变 生物标志物
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复合诱变和抗性筛选利迪链菌素高产菌株 被引量:6
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作者 郭卫寰 李小兵 元英进 《微生物学通报》 CAS CSCD 北大核心 2007年第5期831-835,共5页
为解决利迪链霉菌生产能力低的问题,以Streptomyces lydicus AS4.2501-P28为出发菌株,应用紫外和吖啶橙诱变,结合抗生素的抗性筛选,得到稳定高产的S.lydicus AS4.2501-L8,发酵水平达到177.0μg/mL,较出发菌株提高了96.2%。
关键词 利迪链霉菌 利迪链菌素 复合诱变 抗性筛选
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HIV蛋白酶抑制剂——利迪链菌素的分子对接研究
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作者 李金涛 李艳妮 元英进 《化学学报》 SCIE CAS CSCD 北大核心 2006年第24期2491-2495,共5页
用分子对接的方法,对利迪链菌素的抗HIV蛋白酶活性进行了研究.为了更准确地反映利迪链菌素分子与酶蛋白结合的情况,充分考虑受体活性部位的柔性,采用了FlexX(初步对接)和Flexidock(精确对接)分两步将配体与受体进行对接.在初步对接中,... 用分子对接的方法,对利迪链菌素的抗HIV蛋白酶活性进行了研究.为了更准确地反映利迪链菌素分子与酶蛋白结合的情况,充分考虑受体活性部位的柔性,采用了FlexX(初步对接)和Flexidock(精确对接)分两步将配体与受体进行对接.在初步对接中,设计了不同的受体活性部位来考察是否有结合水分子参与抑制剂与酶的结合.对一种作用方式已知的非肽类HIV蛋白酶抑制剂Aha006进行的对接研究显示,分子模拟的结果与实际情况吻合得较好,证明了本文所采用的方法的可靠性.利迪链菌素与蛋白酶活性部位的对接结果显示,配体分子与受体之间的结合没有结合水分子的参与,两者通过5对氢键作用结合成为稳定的复合物.利迪链菌素占据结合腔,覆盖了蛋白酶的活性三联体Asp25-Thr26-Gly27,从而起到抑制其生物活性的作用. 展开更多
关键词 HIV-1蛋白酶抑制剂 利迪链菌素 分子模拟 分子对接
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