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1.
Appl Microbiol Biotechnol ; 100(22): 9423-9437, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27654657

ABSTRACT

The fermentation process of l-lactic acid is well known. Little importance was attached to d-lactic acid, but in the past 10 years, d-lactic acid gained significantly in importance. d-Lactic acid is an interesting precursor for manufacturing heat-resistant polylactic acid (PLA) bioplastics which can be widely used, for example as packaging material, coatings, for textiles or in the automotive industry.This review provides a comprehensive overview of the most recent developments, including a spectrum of studied microorganisms and their capabilities for the production of d-lactic acid. Additionally, the technological achievements in biotechnological d-lactic acid production including fermentation techniques like fed batch, simultaneous saccharification, and fermentation and continuous techniques are presented. Attention is also turned to suitable alternative substrates and their applicability in fermentation processes. Furthermore, advantages and disadvantages of product recovery and purification are discussed. Economic aspects of PLA are pointed out, and the present industrial producers of lactic acid are briefly introduced.


Subject(s)
Biotechnology/methods , Lactic Acid/isolation & purification , Lactic Acid/metabolism , Biotechnology/trends , Fermentation
2.
Chembiochem ; 15(2): 213-6, 2014 Jan 24.
Article in English | MEDLINE | ID: mdl-24399794

ABSTRACT

The biosynthesis of terpenes is catalysed by class I and II terpene cyclases. Here we present structural data from a class I hedycaryol synthase in complex with nerolidol, serving as a surrogate for the reaction intermediate nerolidyl diphosphate. This prefolded ligand allows mapping of the active site and hence the identification of a key carbonyl oxygen of Val179, a highly conserved helix break (G1/2) and its corresponding helix dipole. Stabilising the carbocation at the substrate's C1 position, these elements act in concert to catalyse the 1,10 ring closure, thereby exclusively generating the anti-Markovnikov product. The delineation of a general mechanistic scaffold was confirmed by site-specific mutations. This work serves as a basis for understanding carbocation chemistry in enzymatic reactions and should contribute to future application of these enzymes in organic synthesis.


Subject(s)
Ligases/metabolism , Sesquiterpenes/metabolism , Terpenes/metabolism , Crystallography, X-Ray , Hydrogen-Ion Concentration , Ligases/chemistry , Ligases/genetics , Models, Molecular , Mutagenesis , Mutation , Protein Binding , Protein Structure, Secondary , Streptomycetaceae/enzymology
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