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Cloning of the Pseudomonas aeruginosa gene encoding CDP-diglyceride synthetase
Affiliation:1. King Abdullah University of Science and Technology (KAUST), BESE Division, 23955-6900 Thuwal, Saudi Arabia;2. Faculty of Agriculture, Cairo University, 12613, Giza, Egypt;3. Department of Plant Sciences and Plant Pathology, Montana State University, Bozeman, MT 59717, USA;1. Max Planck Institute for Medical Research, Department of Cellular Biophysics, Jahnstraße 29, D 69120, Heidelberg, Germany;2. Department of Biophysical Chemistry, University of Heidelberg, Im Neuenheimer Feld 253, D 69120 Heidelberg, Germany;1. Renewable Energy Resources Lab (RERL), Department of Mechanical and Aerospace Engineering, The University of California, Irvine, CA, 92697-3975, USA;2. State Key Lab of Power Systems, International Joint Laboratory on Low Carbon Clean Energy, Innovation, Department of Energy and Power Engineering, Tsinghua University, Beijing, 100084, China;1. Department of Nutrition and Dietetics, Institute of Health Sciences, Istanbul Medipol University, Kavacik South Campus, Beykoz, 34810 Istanbul, Turkey;2. Department of Nutrition and Dietetics, Faculty of Health Sciences, Istanbul Medeniyet University, Kartal Cevizli Campus, Kartal, 34862 Istanbul, Turkey
Abstract:The CDP-diglyceride synthetase (CDS)-encoding gene (cds) from Pseudomonas aeruginosa PAO1 was cloned and sequenced. The gene possessed an open reading frame of 813 bp capable of encoding a putative polypeptide of 271 amino acids (aa) (28 699 Da). The deduced aa sequence of CDS revealed a 67% similarity (45% identity) to Escherichia coli CDS.
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