血红素
大肠杆菌
生物化学
原卟啉IX
球形红杆菌
辅因子
生物
铁螯合酶
血红素蛋白
原卟啉原氧化酶
化学
酶
基因
有机化学
光合作用
光动力疗法
作者
Stephanie Pranawidjaja,Su-In Choi,Bibiana W. Lay,Pil Kim
出处
期刊:Journal of Microbiology and Biotechnology
[Springer Science+Business Media]
日期:2015-06-28
卷期号:25 (6): 880-886
被引量:26
标识
DOI:10.4014/jmb.1411.11050
摘要
Bacterial heme was produced from a genetic-engineered Escherichia coli via the porphyrin pathway and it was useful as an iron resource for animal feed.The amount of the E. colisynthesized heme, however, was only few milligrams in a culture broth and it was not enough for industrial applications.To analyze heme biosynthetic pathways, an engineered E. coli artificially overexpressing ALA synthase (hemA from Rhodobacter sphaeroides) and pantothenate kinase (coaA gene from self geneome) was constructed as a bacterial heme-producing strain, and both the transcription levels of pathway genes and the intermediates concentrations were determined from batch and continuous cultures.Transcription levels of the pathway genes were not significantly changed among the tested conditions.Intracellular intermediate concentrations indicated that aminolevulinic acid (ALA) and coenzyme A (CoA) were enhanced by the hemA-coaA co-expression.Intracellular coproporphyrinogen I and protoporphyrin IX accumulation suggested that the bottleneck steps in the heme biosynthetic pathway could be the spontaneous conversion of HMB to coproporphyrinogen I and the limited conversion of protoporphyrin IX to heme, respectively.A strategy to increase the conversion of ALA to heme is discussed based on the results.
科研通智能强力驱动
Strongly Powered by AbleSci AI