A biosynthetic pathway using pivalic acid as a starter unit was found in three bacterial species, Alicyclobacillus acidoterrestris, Rhodococcus erythropolis and Streptomyces avermitilis. When deuterium-labelled pivalic acid was added to A. acidoterrestris and R. erythropolis nutrient media it was incorporated into fatty acids to give rise to tert-butyl fatty acids (t-FAs). In addition, in R. erythropolis, pivalic acid was transformed into two starter units, i.e. isobutyric and 2-methylbutyric acid, which served as precursors of corresponding iso-even FAs and anteiso-FAs. In S. avermitilis the biosynthesis also yielded all three branched FAs; apart from this pathway, both pivalic and 2-methylbutyric acids were incorporated into the antibiotic avermectin.

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1462-2920.2011.02465.xDOI Listing

Publication Analysis

Top Keywords

pivalic acid
16
starter unit
8
biosynthetic pathway
8
pathway pivalic
8
fatty acids
8
pivalic
5
acid
5
acid acts
4
acts starter
4
unit fatty
4

Similar Publications

Article Synopsis
  • Researchers created tetranuclear clusters of lanthanide (Ln) elements by combining specific salts with a unique phosphinic acid and pivalic acid.* -
  • X-ray studies confirmed the structure of these complexes, which included erbium (Er), dysprosium (Dy), and terbium (Tb), showing distinct magnetic properties.* -
  • Direct-current studies indicated ferromagnetic interactions between Dy and Tb, while Er exhibited antiferromagnetic behavior; both exhibited characteristics of single-molecule magnets.*
View Article and Find Full Text PDF

Fe(II) carboxylates react with dioxygen and carboxylic acid to form Fe(μ-OH)(μ-O)(μ-X)(HX) (X = acetate or pivalate), which is an active oxidant for Rh-catalyzed arene alkenylation. Heating (150-200 °C) the catalyst precursor [(η-CH)Rh(μ-OAc)] with ethylene, benzene, Fe(II) carboxylate, and dioxygen yields styrene >30-fold faster than the reaction with dioxygen in the absence of the Fe(II) carboxylate additive. It is also demonstrated that Fe(μ-OH)(μ-O)(μ-X)(HX) is an active oxidant under anaerobic conditions, and the reduced material can be reoxidized to Fe(μ-OH)(μ-O)(μ-X)(HX) by dioxygen.

View Article and Find Full Text PDF

Rhodium-Catalyzed Oxidative Alkenylation of Anisole: Control of Regioselectivity.

Organometallics

June 2024

Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904, United States.

We report the conversion of anisoles and olefins to alkenyl anisoles via a transition-metal-catalyzed arene C-H activation and olefin insertion mechanism. The catalyst precursor, [(η-CH)Rh(μ-OAc)], and the in situ oxidant Cu(OPiv) (OPiv = pivalate) convert anisoles and olefins (ethylene or propylene) to alkenyl anisoles. When ethylene is used as the olefin, the // ratio varies between approximately 1:3:1 (selective for 3-methoxystyrene) and 1:5:10 (selective for 4-methoxystyrene).

View Article and Find Full Text PDF

East Africa ( spp.), notably , "Matooke" a staple and economically important food in the region. Here, 12 selected .

View Article and Find Full Text PDF

Interaction of the pre-organized complex of iron(II) trimethylacetate and 1,10-phenanthroline (phen) [Fe(piv)(phen)] () (piv = (Me)CCO)) with 1,6-diaminohexane (dahx) in anhydrous acetonitrile yielded a 1D coordination polymer [FeO(piv)(dahx)] () and an organic salt of pivalic acid (Hdahx)(piv) (). The structure of the obtained compounds was determined by single-crystal X-ray diffraction analysis. The phase purity of the complexes was determined by powder X-ray diffraction analysis.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!