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Helga Ertesvåg

Researcher at Norwegian University of Science and Technology

Publications -  63
Citations -  2763

Helga Ertesvåg is an academic researcher from Norwegian University of Science and Technology. The author has contributed to research in topics: Azotobacter vinelandii & Pseudomonas fluorescens. The author has an hindex of 26, co-authored 57 publications receiving 2366 citations.

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Genome Sequence of Azotobacter vinelandii, an Obligate Aerobe Specialized To Support Diverse Anaerobic Metabolic Processes

TL;DR: The complete genome sequence of A. vinelandii DJ is reported, which identified the chromosomal locations of the genes coding for the three known oxygen-sensitive nitrogenases, as well as genes codes for other oxygen- sensitive enzymes, such as carbon monoxide dehydrogenase and formate dehydrogen enzyme.
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Biosynthesis and applications of alginates

TL;DR: Alginates may become useful in applications where reproducible and specific physical properties are required and be used to modify alginates in vitro to obtain polysaccharides with the desired content and distribution pattern of G.
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The Pseudomonas fluorescens AlgG Protein, but Not Its Mannuronan C-5-Epimerase Activity, Is Needed for Alginate Polymer Formation

TL;DR: The isolation of four different epimerization-defective point mutants of the periplasmic Pseudomonas fluorescens mannuronan C-5-epimerase AlgG is reported, showing the formation of two distinct classes of polymers in a genetically pure cell line.
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A family of modular type mannuronan c-5-epimerase genes controls alginate structure in azotobacter vinelandii

TL;DR: It is shown that the Azotobacter vinelandii organism encodes at least four other ME genes originating from a common ancestor gene by a complex rearrangement process, which may explain the origin of the structural variability found in alginates isolated both from prokaryotic and eukaryotic organisms.
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Thraustochytrids as Production Organisms for Docosahexaenoic Acid (DHA), Squalene, and Carotenoids

TL;DR: The present review extracts main findings from the high number of reports on process optimization for DHA production and interpret these in the light of the current knowledge of DHA synthesis in thraustochytrids and lipid accumulation in oleaginous microorganisms in general.