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Augmented biosynthesis of cadmium sulfide nanoparticles by genetically engineered Escherichia coli
Biotechnology progress, 2009-09, Vol.25 (5), p.1260-1266
Chen, Yen-Lin
Tuan, Hsing-Yu
Tien, Chun-Wen
Lo, Wen-Hsin
Liang, Huang-Chien
Hu, Yu-Chen
2009
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Chen, Yen-Lin
Tuan, Hsing-Yu
Tien, Chun-Wen
Lo, Wen-Hsin
Liang, Huang-Chien
Hu, Yu-Chen
Titel
Augmented biosynthesis of cadmium sulfide nanoparticles by genetically engineered Escherichia coli
Ist Teil von
Biotechnology progress, 2009-09, Vol.25 (5), p.1260-1266
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2009
Quelle
Access via Wiley Online Library
Beschreibungen/Notizen
Microorganisms can complex and sequester heavy metals, rendering them promising living factories for nanoparticle production. Glutathione (GSH) is pivotal in cadmium sulfide (CdS) nanoparticle formation in yeasts and its synthesis necessitates two enzymes: γ‐glutamylcysteine synthetase (γ‐GCS) and glutathione synthetase (GS). Hereby, we constructed two recombinant E. coli ABLE C strains to over‐express either γ‐GCS or GS and found that γ‐GCS over‐expression resulted in inclusion body formation and impaired cell physiology, whereas GS over‐expression yielded abundant soluble proteins and barely impeded cell growth. Upon exposure of the recombinant cells to cadmium chloride and sodium sulfide, GS over‐expression augmented GSH synthesis and ameliorated CdS nanoparticles formation. The resultant CdS nanoparticles resembled those from the wild‐type cells in size (2–5 nm) and wurtzite structures, yet differed in dispersibility and elemental composition. The maximum particle yield attained in the recombinant E. coli was ≈2.5 times that attained in the wild‐type cells and considerably exceeded that achieved in yeasts. These data implicated the potential of genetic engineering approach to enhancing CdS nanoparticle biosynthesis in bacteria. Additionally, E. coli‐based biosynthesis offers a more energy‐efficient and eco‐friendly method as opposed to chemical processes requiring high temperature and toxic solvents. © 2009 American Institute of Chemical Engineers Biotechnol. Prog., 2009
Sprache
Englisch
Identifikatoren
ISSN: 8756-7938, 1520-6033
eISSN: 1520-6033
DOI: 10.1002/btpr.199
Titel-ID: cdi_proquest_miscellaneous_888109053
Format
–
Schlagworte
Biological and medical sciences
,
Biotechnology
,
Cadmium Chloride - metabolism
,
Cadmium Compounds - chemistry
,
Cadmium Compounds - metabolism
,
cadmium sulfide (CdS)
,
Cell Proliferation
,
Cloning, Molecular - methods
,
Escherichia coli
,
Escherichia coli - genetics
,
Escherichia coli - metabolism
,
Fundamental and applied biological sciences. Psychology
,
Fungal Proteins - genetics
,
Fungal Proteins - metabolism
,
genetic engineering
,
Glutamate-Cysteine Ligase - genetics
,
Glutamate-Cysteine Ligase - metabolism
,
glutathione
,
Glutathione Synthase - genetics
,
Glutathione Synthase - metabolism
,
glutathione synthetase
,
glutathione, glutathione synthetase
,
Metal Nanoparticles - chemistry
,
Microscopy, Electron, Transmission
,
nanoparticles
,
Spectrometry, X-Ray Emission
,
Sulfides - chemistry
,
Sulfides - metabolism
,
Yeasts - enzymology
,
Yeasts - genetics
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