TY - CHAP
T1 - Analysing intracellular isoprenoid metabolites in diverse prokaryotic and eukaryotic microbes
AU - Plan, Manuel
AU - Bongers, Mareike
AU - Bydder, Sarah
AU - Fabris, Michele
AU - Hodson, Mark P.
AU - Kelly, Erin
AU - Krömer, Jens
AU - Perez-Gil, Jordi
AU - Peng, Bingyin
AU - Satta, Alessandro
AU - Schrübbers, Lars C.
AU - Vickers, Claudia E.
PY - 2022
Y1 - 2022
N2 - Isoprenoids, also known as terpenes or terpenoids, are a very large and diverse group of natural compounds. These compounds fulfil a myriad of critical roles in biology as well as having a wide range of industrial uses. Isoprenoids are produced via two chemically distinct metabolic pathways, the mevalonate (MVA) pathway and the methylerythritol phosphate (MEP) pathway. Downstream of these two pathways is the shared prenyl phosphate pathway. Because of their importance in both basic physiology and industrial biotechnology, extraction, identification, and quantification of isoprenoid pathway intermediates is an important protocol. Here we describe methods for extraction and analysis of intracellular metabolites from the MVA, MEP, and prenyl phosphate pathways for five key model microbes: the yeast Saccharomyces cerevisiae, the bacterium Escherichia coli, the diatom Phaeodactylum tricornutum, the green algae Chlamydomonas reinhardtii, and the cyanobacterium Synechocystis sp. PCC 6803. These methods also detect several central carbon intermediates. These protocols will likely work effectively, or be readily adaptable, to a variety of related microorganisms and metabolic pathways.
AB - Isoprenoids, also known as terpenes or terpenoids, are a very large and diverse group of natural compounds. These compounds fulfil a myriad of critical roles in biology as well as having a wide range of industrial uses. Isoprenoids are produced via two chemically distinct metabolic pathways, the mevalonate (MVA) pathway and the methylerythritol phosphate (MEP) pathway. Downstream of these two pathways is the shared prenyl phosphate pathway. Because of their importance in both basic physiology and industrial biotechnology, extraction, identification, and quantification of isoprenoid pathway intermediates is an important protocol. Here we describe methods for extraction and analysis of intracellular metabolites from the MVA, MEP, and prenyl phosphate pathways for five key model microbes: the yeast Saccharomyces cerevisiae, the bacterium Escherichia coli, the diatom Phaeodactylum tricornutum, the green algae Chlamydomonas reinhardtii, and the cyanobacterium Synechocystis sp. PCC 6803. These methods also detect several central carbon intermediates. These protocols will likely work effectively, or be readily adaptable, to a variety of related microorganisms and metabolic pathways.
KW - Chlamydomonas reinhardtii
KW - Escherichia coli
KW - Intracellular metabolites
KW - Isoprenoids
KW - Methylerythritol phosphate pathway
KW - Mevalonate pathway
KW - Phaeodactylum tricornutum
KW - Prenyl phosphate metabolism
KW - Saccharomyces cerevisiae
KW - Synechocystis sp. PCC 6803
KW - Terpenoids
UR - http://www.scopus.com/inward/record.url?scp=85128677722&partnerID=8YFLogxK
U2 - 10.1016/bs.mie.2022.03.018
DO - 10.1016/bs.mie.2022.03.018
M3 - Chapter
C2 - 35871838
SN - 9780323999755
T3 - Methods in Enzymology
SP - 235
EP - 284
BT - Carotenoids
A2 - Wurtzel, Eleanore T.
PB - Elsevier
CY - Cambridge, MA
ER -