A fully enzymatic esterification/transesterification sequence for the preparation of symmetrical and unsymmetrical trehalose diacyl conjugates

TL;DR: The purpose of this chapter is to study the effectiveness of various biosurfactant-producing bacteria and their potent role in heavy metal remediation.

TL;DR: Trehalose fatty acid esters can find potential applications in pharmaceuticals, functional foods, and nutraceuticals, as well as against four bacterial, and two fungal species.

TL;DR: The hydrophile-lipophile balance (HLB) values, foaming properties and emulsifying properties of trehalose diesters were assessed, showing the potentials of these diesters as naturally derived surfactants for the food industry.

TL;DR: The LIT MSn approach to unveil the structures of a 2,3-diacyl trehalose (DAT) family isolated from the cell envelope of Mycobacterium tuberculosis, in which more than 30 molecular species, and each species consisting of up to six isomeric structures were found.

TL;DR: In this paper, a novel synthetic route to cyclopropanes by the reaction of olefins with dialkylzinc and methylene iodide is described, which is similar to that of the Simmons-Smith reaction.

TL;DR: The current knowledge of trehalolipid biosurfactant applications and the latest successful strategies employed to reduce the cost of their production are highlighted.

TL;DR: The observed kinetic behavior of all the esterification reactions is found to follow a ping-pong bi-bi mechanism with competitive inhibition by both substrates.