Biosynthesis of isoprenoids (carotenoids, sterols, prenyl side-chains of chlorophylls and plastoquinone) via a novel pyruvate/glyceraldehyde 3-phosphate non-mevalonate pathway in the green alga Scenedesmus obliquus

Algal Physiology and Biochemistry.

Baalen, C. V., & Stewart, W. P. D. (1975) · Bulletin of the Torrey Botanical Club · doi:10.2307/2484419 · Cited by 1,453

Isoprenoid biosynthesis in bacteria: a novel pathway for the early steps leading to isopentenyl diphosphate

Rohmer, M., Knani, M., Simonin, P., Sutter, B., & Sahm, H. (1993) · Biochemical Journal · doi:10.1042/bj2950517 · Cited by 1,200

The Biochemistry of the Carotenoids

Goodwin, T. W. (1984) · Springer eBooks · doi:10.1007/978-94-009-5542-4 · Cited by 1,010

Terpenoid Metabolism

McGarvey, D. J., & Croteau, R. (1995) · The Plant Cell · doi:10.1105/tpc.7.7.1015 · Cited by 722

The Biochemistry of the Carotenoids

Goodwin, T. W. (1980) · Springer eBooks · doi:10.1007/978-94-009-5860-9 · Cited by 613

Biosynthesis of isoprenoid compounds

(1982) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(82)90284-5 · Cited by 557

Carbon-13nmr spectroscopy

Moore, G. R. (1989) · Spectrochimica Acta Part A Molecular Spectroscopy · doi:10.1016/0584-8539(89)80139-4 · Cited by 401

Biosynthesis of isoprenoid compounds

(1982) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(82)90032-5 · Cited by 372

Some new aspects of isoprenoid biosynthesis in plants—A review

Bach, T. J. (1995) · Lipids · doi:10.1007/bf02537822 · Cited by 301

Prokaryotic hopanoids: the biosynthesis of the bacteriohopane skeleton: Formation of isoprenic units from two distinct acetate pools and a novel type of carbon/carbon linkage between a triterpene and d‐ribose

FLESCH, G., & ROHMER, M. (1988) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1988.tb14210.x · Cited by 233

De NovoTranscriptome Sequencing of the Orange-Fleshed Sweet Potato and Analysis of Differentially Expressed Genes Related to Carotenoid Biosynthesis

Li, R., Zhai, H., Chen, K., Liu, D., He, S., & Liu, Q. (2015) · International Journal of Genomics · doi:10.1155/2015/843802 · Cited by 33

Metabolite Transporters in the Control of Plant Primary Metabolism

Tegeder, M., & Weber, A. P. M. (2007) · Blackwell Publishing Ltd eBooks · doi:10.1002/9780470988640.ch4 · Cited by 31

Biosynthesis of Phytol in the Cyanobacterium Synechocystis sp. UTEX 2470: Utilization of the Non-Mevalonate Pathway

Proteau, P. (1998) · Journal of Natural Products · doi:10.1021/np980006q · Cited by 32

Designer labels for plant metabolism: statistical design of isotope labeling experiments for improved quantification of flux in complex plant metabolic networks

Nargund, S., & Sriram, G. (2012) · Molecular BioSystems · doi:10.1039/c2mb25253h · Cited by 31

Differential gene expression for carotenoid biosynthesis in a green alga Ulva prolifera based on transcriptome analysis

He, Y., Ma, Y., Du, Y., & Shen, S. (2018) · BMC Genomics · doi:10.1186/s12864-018-5337-y · Cited by 31

Biosynthesis of Isoprene Units in the C34 Botryococcene Molecule Produced by Botryococcus Braunii Strain Bot-22

Ishimatsu, A., Matsuura, H., Sano, T., Kaya, K., & Watanabe, M. M. (2012) · Procedia Environmental Sciences · doi:10.1016/j.proenv.2012.05.010 · Cited by 31

Methylerythritol Phosphate Pathway

Rohmer, M. (2010) · Elsevier eBooks · doi:10.1016/b978-008045382-8.00702-4 · Cited by 29

Biosynthesis of the dimethylallyl moiety of novobiocin via a non-mevalonate pathway

Li, S.-M., Hennig, S., & Heide, L. E. (1998) · Tetrahedron Letters · doi:10.1016/s0040-4039(98)00386-4 · Cited by 29

Effects of fosmidomycin on plant photosynthesis as measured by gas exchange and chlorophyll fluorescence

Possell, M., Ryan, A. C., Vickers, C. E., Mullineaux, P. M., & HEWITT, C. N. (2009) · Photosynthesis Research · doi:10.1007/s11120-009-9504-5 · Cited by 28

Genotypic abundance of carotenoids and polyphenolics in the hull of field pea (Pisum sativum L.)

Marles, M. A. S., Warkentin, T. D., & Bett, K. E. (2012) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.5782 · Cited by 28

Origin of two isoprenoid units in a lavandulyl moiety of sophoraflavanone G from Sophora flavescens cultured cells

Yamamoto, H. (2002) · Phytochemistry · doi:10.1016/s0031-9422(02)00111-5 · Cited by 28

Chapter 7 The Non-mevalonate DOXP/MEP (Deoxyxylulose 5-Phosphate/Methylerythritol 4-Phosphate) Pathway of Chloroplast Isoprenoid and Pigment Biosynthesis

Lichtenthaler, H. K. (2010) · Advances in photosynthesis and respiration · doi:10.1007/978-90-481-8531-3_7 · Cited by 27

Cofactor Biosynthesis: A Mechanistic Perspective

Begley, T. P., Kinsland, C. L., Taylor, S. V., Tandon, M., Nicewonger, R., Wu, M., Chiu, H., Kelleher, N. L., Campobasso, N., & Zhang, Y. (1998) · Topics in current chemistry · doi:10.1007/3-540-69542-7_3 · Cited by 26

Identification of an allele of CLA1 associated with variegation in Arabidopsis thaliana

Crowell, D. N., Packard, C. E., Pierson, C. A., Giner, J., Downes, B. P., & Chary, S. N. (2003) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2003.00063.x · Cited by 26

Ishigoside, a new glyceroglycolipid isolated from the brown alga Ishige okamurae

Zou, Y., Li, Y., Kim, M., Lee, S., & Kim, S. (2009) · Biotechnology and Bioprocess Engineering · doi:10.1007/s12257-008-0131-3 · Cited by 25

Structure of 2C-methyl- D -erythritol-2,4-cyclodiphosphate synthase fromShewanella oneidensisat 1.6 Å: identification of farnesyl pyrophosphate trapped in a hydrophobic cavity

Ni, S., Robinson, H. H., Marsing, G. C., Bussiere, D. E., & Kennedy, M. A. (2004) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444904021791 · Cited by 25

Biosynthesis of abietane diterpenoids in cultured cells of Torreya nucifera var. radicans: biosynthetic inequality of the FPP part and the terminal IPP

Yang, J., & Orihara, Y. (2002) · Tetrahedron · doi:10.1016/s0040-4020(01)01232-7 · Cited by 24

Synthesis of 1-Deoxy- d -xylulose and 1-Deoxy- d -xylulose-5-phosphate

Blagg, B. S. J., & Poulter, C. D. (1999) · The Journal of Organic Chemistry · doi:10.1021/jo981966k · Cited by 25

13C/12C Signatures in Plants and Algae

Chikaraishi, Y. (2013) · Elsevier eBooks · doi:10.1016/b978-0-08-095975-7.01008-1 · Cited by 23

Molecular Biosignatures

Summons, R. E., Albrecht, P., McDonald, G. D., & Moldowan, J. M. (2008) · Space sciences series of ISSI · doi:10.1007/978-0-387-77516-6_11 · Cited by 30

Highly Efficient and Versatile Synthesis of Isotopically Labelled 1-Deoxy-D-xylulose

Piel, J., & Boland, W. (1997) · Tetrahedron Letters · doi:10.1016/s0040-4039(97)01448-2 · Cited by 24

Biosynthetic origins of the isoprene units of gaudichaudianic acid in Piper gaudichaudianum (Piperaceae)

Lopes, A. A., Baldoqui, D. C., López, S. N., Kato, M. J., Bolzani, V. D. S., & Furlan, M. (2007) · Phytochemistry · doi:10.1016/j.phytochem.2007.04.025 · Cited by 23

Biosynthesis of unusual monocyclic alkenes by the diatom Rhizosolenia setigera (Brightwell)

Massé, G. (2004) · Phytochemistry · doi:10.1016/j.phytochem.2004.02.019 · Cited by 23

Multigram Synthesis of Mevalonolactone-d9 and Its Application to Stereochemical Analysis by 1H NMR of the Saturation Reaction in the Biosynthesis of the 2,3-Di-O-phytanyl-sn-glycerol Core of the Archaeal Membrane Lipid

Eguchi, T., Morita, M., & Kakinuma, S. (1998) · Journal of the American Chemical Society · doi:10.1021/ja974387q · Cited by 23

Regulation of gibberellin biosynthesis

Hedden, P. (1999) · New comprehensive biochemistry · doi:10.1016/s0167-7306(08)60487-1 · Cited by 23

A Novel Lactobacillus casei LP1 Producing 1,4-Dihydroxy-2-Naphthoic Acid, a Bifidogenic Growth Stimulator

Kang, J.-E., Kim, T., & Moon, G. (2015) · Preventive Nutrition and Food Science · doi:10.3746/pnf.2015.20.1.78 · Cited by 22

Microbial Production of Isoprenoids

Wong, J., Rios‐Solis, L., & Keasling, J. D. (2017) · Springer eBooks · doi:10.1007/978-3-319-50436-0_219 · Cited by 21

Carbon isotope-labelling experiments indicate that ladderane lipids of anammox bacteria are synthesized by a previously undescribed, novel pathway

Rattray, J. E., Geenevasen, J. A. J., van Niftrik, L., Rijpstra, W. I. C., Hopmans, E. C., Strous, M., Stefan Schouten, A., Jetten, M. S. M., & Damsté, J. S. S. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2008.01483.x · Cited by 22

Biosynthetic Pathway for the C45 Polyprenol, Solanesol, in Tobacco

Fukusaki, E., Takeno, S., Bamba, T., Okumoto, H., Katto, H., Kajiyama, S.-I., & Kobayashi, A. (2004) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.68.1988 · Cited by 22

Synthesis, Export and Partitioning of the End Products of Photosynthesis

Weber, A. P. M. (2007) · Advances in photosynthesis and respiration · doi:10.1007/978-1-4020-4061-0_14 · Cited by 22

Crystal structure of 1-deoxy-d-xylulose 5-phosphate reductoisomerase from the hyperthermophile Thermotoga maritima for insights into the coordination of conformational changes and an inhibitor binding

Takenoya, M., Ohtaki, A., Noguchi, K., Endo, K., Sasaki, Y., Ohsawa, K., Yajima, S., & Yohda, M. (2010) · Journal of Structural Biology · doi:10.1016/j.jsb.2010.03.015 · Cited by 21

Biosynthesis of plaunotol in Croton stellatopilosus proceeds via the deoxyxylulose phosphate pathway

Wungsintaweekul, J., & De‐Eknamkul, W. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.01.122 · Cited by 21

Stereochemistry of hydrogen introduction at C-25 in ergosterol synthesized by the mevalonate-independent pathway

Zhou, W., & Nes, W. D. (2000) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)00265-3 · Cited by 21

Biosynthesis of isoprenic units via different pathways: Occurrence and future prospects

Knöß, W., & Reuter, B. (1998) · Pharmaceutica Acta Helvetiae · doi:10.1016/s0031-6865(97)00046-0 · Cited by 21

Analysis of plant secondary metabolism using stable isotope‐labelled precursors

Arroo, R., Bhambra, A. S., Hano, C., Renda, G., Ruparelia, K. C., & Wang, M. F. (2020) · Phytochemical Analysis · doi:10.1002/pca.2955 · Cited by 20

Climate Change: Challenges to Reduce Global Warming and Role of Biofuels

Kumar, A. (2020) · Springer eBooks · doi:10.1007/978-981-15-5228-1_2 · Cited by 21

A Structure-Based Approach to Ligand Discovery for 2C-Methyl- d -erythritol-2,4-cyclodiphosphate Synthase: A Target for Antimicrobial Therapy

Ramsden, N. L., Buetow, L., Dawson, A., Kemp, L. E., Ulaganathan, V., Brenk, R., Klebe, G., & Hunter, W. N. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm801475n · Cited by 20

The use of genome-scale metabolic network reconstruction to predict fluxes and equilibrium composition of N-fixing versus C-fixing cells in a diazotrophic cyanobacterium, Trichodesmium erythraeum

Gardner, J. J., & Boyle, N. R. (2017) · BMC Systems Biology · doi:10.1186/s12918-016-0383-z · Cited by 19

Molecular Engineering of Monoterpene Production

Haudenschild, C. D., & Croteau, R. (1998) · Springer eBooks · doi:10.1007/978-1-4899-1739-3_14 · Cited by 19

Metabolic flux analysis of the two astaxanthin‐producing microorganisms Haematococcus pluvialis and Phaffia rhodozyma in the pure and mixed cultures

Dong, Q., Zhao, X., Ma, H., Xing, X., & Sun, N. (2006) · Biotechnology Journal · doi:10.1002/biot.200600060 · Cited by 19

Biosynthetic Pathway of β-Thujaplicin in the Cupressus lusitanica Cell Culture

Fujita, K., Yamaguchi, T., Itose, R., & Sakai, K. (2000) · Journal of Plant Physiology · doi:10.1016/s0176-1617(00)80160-1 · Cited by 18

Biosynthesis of Chloroplastidic and Extrachloroplastidic Terpenoids in Liverwort Cultured Cells: 13C Serine as a Probe of Terpene Biosynthesis via Mevalonate and Non-mevalonate Pathways

Itoh, D., Kawano, K., & Nabeta, K. (2003) · Journal of Natural Products · doi:10.1021/np0204141 · Cited by 18

Comparative Protein Modeling of 1-Deoxy- d -xylulose-5-phosphate Reductoisomerase Enzyme from Plasmodium falciparum: A Potential Target for Antimalarial Drug Discovery

Singh, N., Chevé, G., Avery, M. A., & McCurdy, C. R. (2006) · Journal of Chemical Information and Modeling · doi:10.1021/ci050523w · Cited by 18

YGL3 Encoding an IPP and DMAPP Synthase Interacts with OsPIL11 to Regulate Chloroplast Development in Rice

Chen, W., Tang, L., Li, Q., Cai, Y., Ahmad, S., Wang, Y., Tang, S., Guo, N., Wei, X., Tang, S., et al. (2024) · Rice · doi:10.1186/s12284-024-00687-y · Cited by 18

Phytohormones and Pheromones in the Phycology Literature: Benchmarking of Data-Set and Developing Critical Tools of Biotechnological Implications for Commercial Aquaculture Industry

Rathod, S. G., Bhushan, S., & Mantri, V. A. (2023) · Phycology · doi:10.3390/phycology4010001 · Cited by 20

A convenient synthesis of 2-C-methyl-d-erythritol 4-phosphate and isotopomers of its precursor

Koumbis, A. E., Kotoulas, S. S., & Gallos, J. K. (2006) · Tetrahedron · doi:10.1016/j.tet.2006.12.078 · Cited by 17

Enzymatic synthesis of 1-deoxysugar-phosphates using E. coli 1-deoxy-d-xylulose 5-phosphate synthase

Querol‐Audí, J., Grosdemange‐Billiard, C., Rohmer, M., Boronat, A., & Imperial, S. (2002) · Tetrahedron Letters · doi:10.1016/s0040-4039(02)02018-x · Cited by 17

Nitrogen and Carbon Metabolism in Plastids: Evolution, Integration, and Coordination with Reactions in the Cytosol

Tobin, A. K., & Bowsher, C. (2005) · Advances in botanical research · doi:10.1016/s0065-2296(05)42004-2 · Cited by 17

Recognition of n-alkyl and isoprenoid algaenans in marine sediments by stable carbon isotopic analysis of pyrolysis products of kerogens

Höld, I. M., Stefan Schouten, A., Kaam-Peters, H. M. E. V., & Damsté, J. S. S. (1998) · Organic Geochemistry · doi:10.1016/s0146-6380(97)00130-7 · Cited by 17

Biomarkers (Organic, Compound-Specific Isotopes)

Grice, K., & Brocks, J. J. (2011) · Encyclopedia of earth sciences series/Encyclopedia of earth sciences · doi:10.1007/978-1-4020-9212-1_29 · Cited by 17

Genetic Adaptation of a Mevalonate Pathway Deficient Mutant in Staphylococcus aureus

Reichert, S., Ebner, P., Bonetti, E.-J., Luqman, A., Nega, M., Schrenzel, J., Spröer, C., Bunk, B., Overmann, J., Saß, P., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01539 · Cited by 15

Isotope tracer investigations of natural products biosynthesis: the discovery of novel metabolic pathways

Mahmud, T. (2007) · Journal of Labelled Compounds and Radiopharmaceuticals · doi:10.1002/jlcr.1391 · Cited by 16

Terpenes

Humphrey, A. J., & Beale, M. H. (2006) · doi:10.1002/9780470988558.ch3 · Cited by 16

Biosynthesis, Localization and Concentration of Carotenoids in Plants and Algae

Lichtenthaler, H. K. (2011) · Advances in photosynthesis and respiration · doi:10.1007/978-94-007-1579-0_4 · Cited by 15

Biosynthesis of the gymnomitrane-type sesquiterpenes in liverworts

Warmers, U., & König, W. Α. (2000) · Phytochemistry · doi:10.1016/s0031-9422(99)00587-7 · Cited by 15

Induction Mechanism of 3-Hydroxy-3-methylglutaryl-CoA Reductase in Potato Tuber and Sweet Potato Root Tissues

KONDO, K., Uritani, I., & Ôba, K. (2003) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.67.1007 · Cited by 15

Enhancement of 1,4-Dihydroxy-2-Naphthoic Acid Production by Propionibacterium freudenreichii ET-3 Fed-Batch Culture

Furuichi, K., Katakura, Y., Ninomiya, K., & Shioya, S. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01307-06 · Cited by 15

The synthesis of 1-fluoro- and 1,1-difluoro- analogues of 1-deoxy-d-xylulose

Bouvet, D. R., & O’Hagan, D. (1999) · Tetrahedron · doi:10.1016/s0040-4020(99)00572-4 · Cited by 15

Biosynthesis of a hopane triterpene and three diterpenes in the liverwort Fossombronia alaskana

Hertewich, U. M., Zapp, J., Becker, H., & Adam, K. P. (2001) · Phytochemistry · doi:10.1016/s0031-9422(01)00359-4 · Cited by 16

Genomics and transcriptomics reveal β-carotene synthesis mechanism in Dunaliella salina

Chen, D., Li, Z., Shi, J., Suen, H., Zheng, X., Zhang, C., Chen, Y., & Xue, T. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1389224 · Cited by 14

The Discovery of Terpenes

Croteau, R. (1998) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789812817563_0020 · Cited by 14

Volatile organic compounds from microalgae

Vieira, K. R., Pinheiro, P. N., & Zepka, L. Q. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818536-0.00024-5 · Cited by 15

Fifty-Five Years of Research on Photosynthesis, Chloroplasts, and Stress Physiology of Plants: 1958–2013

Lichtenthaler, H. K. (2014) · Progress in botany · doi:10.1007/978-3-319-08807-5_1 · Cited by 13

Exploring Biodiversity to Enhance Bioactivity in the Genus Tanacetum through Protoplast Fusion

Keskitalo, M. K. (1999) · Työväentutkimus Vuosikirja · Cited by 12

Plant Hormones

Murofushi, N., Yamane, H., Sakagami, Y., Imaseki, H., Kamiya, Y., Iwamura, H., Hirai, N., Tsuji, H., Yokota, T., & Ueda, J. (1999) · Elsevier eBooks · doi:10.1016/b978-0-08-091283-7.00050-3 · Cited by 12

Antisense expression of hmg1 from Arabidopsis thaliana encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase, reduces isoprenoid production in transgenic tobacco plants

Godoy-Hernández, G. D. C., Chappell, J., Devarenne, T. P., García‐Pineda, E., Guevara-García, Á. A., & Lozoya‐Gloria, E. (1998) · Journal of Plant Physiology · doi:10.1016/s0176-1617(98)80169-7 · Cited by 12

Synthesis of tritium labelled 2-C-methyl-d-erythritol, a useful substrate for the elucidation of the methylerythritol phosphate pathway for isoprenoid biosynthesis

Hoeffler, J., Grosdemange‐Billiard, C., & Rohmer, M. (2000) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)00726-7 · Cited by 12

Taxon-specific hydrogen isotope signals in cultures and mesocosms facilitate ecosystem and hydroclimate reconstruction

Ladd, S. N., Nelson, D. B., Matthews, B., Dyer, S. M., Limberger, R., Klatt, A., Narwani, A., Dubois, N., & Schubert, C. J. (2024) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2024.12.002 · Cited by 11

Synthesis of Abscisic Acid in Neopyropia yezoensis and Its Regulation of Antioxidase Genes Expressions Under Hypersaline Stress

Yang, J., Gu, W., Feng, Z., Yu, B., Niu, J., & Wang, G. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.775710 · Cited by 11

Plant terpene biosynthesis. The biosynthesis of linalyl acetate in Mentha citrata

Fowler, D. J., Hamilton, J. T. G., Humphrey, A. J., & O’Hagan, D. (1999) · Tetrahedron Letters · doi:10.1016/s0040-4039(99)00532-8 · Cited by 11

Pneumocystis carinii f. sp. carinii Synthesizes De Novo Four Homologs of Ubiquinone

Sul, D., & Kaneshiro, E. S. (2001) · Journal of Eukaryotic Microbiology · doi:10.1111/j.1550-7408.2001.tb00301.x · Cited by 11

Engineering Nannochloropsis oceanica for the production of diterpenoid compounds

Du, Z., Bhat, W. W., Poliner, E., Johnson, S. R., Bertucci, C., Farré, E. M., & Hamberger, B. (2023) · mLife · doi:10.1002/mlf2.12097 · Cited by 9

Cloning and functional characterization of an enzyme from Helicobacter pylori that catalyzes two steps of the methylerythritol phosphate pathway for isoprenoid biosynthesis

Pérez-Gil, J., Bergua, M., Boronat, A., & Imperial, S. (2010) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2010.06.008 · Cited by 10

Photoproduction of Aviation Fuel β‐Caryophyllene From the Eukaryotic Green Microalga Chlamydomonas reinhardtii

Dou, X., Li, M., Ge, Y., Yin, G., Wang, X., Xue, S., Jia, B., Zi, L., Wan, H., Xi, Y., et al. (2024) · Biotechnology and Bioengineering · doi:10.1002/bit.28898 · Cited by 9

Practical Synthesis of [3-(2H3)Methyl]mevalonolactone and Incorporation Experiment of [3-(2H3)Methyl]mevalonolactone and [13C]Labeled Acetate in the Biosynthesis of Isoprenoidal Diether Lipids of Halophilic Archaea

Yamauchi, N., Natsubori, Y., & Murae, T. (2000) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.73.2513 · Cited by 9

Trennung eines racemischen Gemisches zweidimensionaler molekularer Cluster mit dem Rastertunnelmikroskop

Böhringer, M., Morgenstern, K., Schneider, W., & Berndt, R. L. (1999) · Angewandte Chemie · doi:10.1002/(sici)1521-3757(19990315)111:6 · Cited by 43

Carotenoid Overproduction in Microalgae: Biochemical and Genetic Engineering

Scarsini, M., Marchand, J., & Schoefs, B. (2020) · Springer eBooks · doi:10.1007/978-3-030-50971-2_5 · Cited by 9

Strepyrrolins A–E, five pyrrole–sesquiterpene hybrids from Streptomyces sp. KIB 015, revealing a new formation logic of pyrroles by isotope labeling

Wang, L., Zhou, Z., Huang, J., Zhang, L., Tuo, X., Yu, Z., Huang, S., Liu, Y., & Yang, J. (2022) · Organic Chemistry Frontiers · doi:10.1039/d2qo01767a · Cited by 8

Microbial Production of Isoprenoids

Wong, J., Rios‐Solis, L., & Keasling, J. D. (2017) · Springer eBooks · doi:10.1007/978-3-319-31421-1_219-2 · Cited by 7

1-DEOXY- D -XYLULOSE SYNTHESIZED FROM THE (S)-CYANOHYDRIN OF ACROLEIN

Fechter, M. H., Gaisberger, R., & Griengl, H. (2001) · Journal of Carbohydrate Chemistry · doi:10.1081/car-100108660 · Cited by 8

Toward Mycobacterium tuberculosis DXR inhibitor design: homology modeling and molecular dynamics simulations

Singh, N., Avery, M. A., & McCurdy, C. R. (2007) · Journal of Computer-Aided Molecular Design · doi:10.1007/s10822-007-9132-0 · Cited by 8

Leaf-level metabolic changes in response to drought affect daytime CO2 emission and isoprenoid synthesis pathways

Ladd, S. N., Daber, L. E., Bamberger, I., Kübert, A., Kreuzwieser, J., Purser, G., Ingrisch, J., Deleeuw, J., van Haren, J. L. M., Meredith, L., et al. (2023) · Tree Physiology · doi:10.1093/treephys/tpad094 · Cited by 7

Microbial Production of Isoprenoids

Keasling, J. D. (2009) · Springer eBooks · doi:10.1007/978-3-540-77587-4_219 · Cited by 7

Transcriptomic Insight into Aroma Pathway Genes and Effect of Ripening Difference on Expression of Aroma Genes in Different Mango Cultivars

Pathak, G., Dudhagi, S. S., Raizada, S., & Sane, V. A. (2022) · Plant Molecular Biology Reporter · doi:10.1007/s11105-022-01355-5 · Cited by 7

Molecular Characterization of cDNAs Encoding 3-Hydroxy-3-methylglutaryl Coenzyme A Reductase in Marigold (Tagetes erecta)

Villar‐Martínez, A. A. D., Ma, R., & Paredes‐López, O. (1999) · Journal of Plant Physiology · doi:10.1016/s0176-1617(99)80008-x · Cited by 7

Heterologous fermentation of a diterpene fromAlternaria brassisicola

Arens, J., Bergs, D., Mewes, M., Merz, J., Schembecker, G., & Schulz, F. (2014) · Mycology: An International Journal on Fungal Biology · doi:10.1080/21501203.2014.917735 · Cited by 7

Synthesis of [5,5-2H2]-1-Deoxy-D-xylulose-5-phosphate

Thiel, R., & Adam, K. (1999) · Tetrahedron Letters · doi:10.1016/s0040-4039(99)01039-4 · Cited by 7

Genetics of Capsular Polysaccharides and Cell Envelope (Glyco)lipids

Daffé, M., Crick, D. C., & Jackson, M. (2015) · ASM Press eBooks · doi:10.1128/9781555818845.ch28 · Cited by 7

Biosynthesis and Emission of Isoprene, Methylbutanol and Other Volatile Plant Isoprenoids

Lichtenthaler, H. K. (2010) · Wiley eBooks · doi:10.1002/9780470669532.ch2 · Cited by 7

Isoprenoids in eukaryotic phytoplankton: Metabolic diversity, eco-physiology, and biotechnological opportunities

Pruckner, F., Morelli, L., & Fabris, M. (2025) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiaf314 · Cited by 6

Considerations and Criteria for the Incorporation of Mechanistic Sublethal Endpoints into Environmental Risk Assessment for Biologically Active Compounds

Brain, R. A., & Brooks, B. W. (2012) · Emerging topics in ecotoxicology · doi:10.1007/978-1-4614-3473-3_7 · Cited by 6

Marrubium vulgare (White Horehound): In Vitro Culture, and the Production of Diterpene Marrubiin and Other Secondary Metabolites

Knöß, W. (1999) · Biotechnology in agriculture and forestry · doi:10.1007/978-3-662-08614-8_16 · Cited by 6

Chapter 11 Transport Processes: Connecting the Reactions of C4 Photosynthesis

Bräutigam, A., & Weber, A. P. M. (2010) · Advances in photosynthesis and respiration · doi:10.1007/978-90-481-9407-0_11 · Cited by 6

Metalloenzymes involved in carotenoid biosynthesis in plants

Davis, I., Geng, J., & Liu, A. (2022) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2022.01.012 · Cited by 6

Mathematical Modeling of Isotope Labeling Experiments for Metabolic Flux Analysis

Nargund, S., & Sriram, G. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-661-0_8 · Cited by 6

δ13C as an Indicator of Palaeoenvironments

Grice, K. (2001) · Current plant science and biotechnology in agriculture · doi:10.1007/978-94-015-9841-5_12 · Cited by 6

Prenyltransferase

Kurokawa, H., & Koyama, T. (2010) · Elsevier eBooks · doi:10.1016/b978-008045382-8.00002-2 · Cited by 6

De Novo Synthesis of Monosaccharides

Vogel, P. (2001) · Springer eBooks · doi:10.1007/978-3-662-11893-1_4 · Cited by 6

A Novel Mevalonate-Independent Pathway for the Biosynthesis of Carotenoids, Phytol and Prenyl Chain of Plastoquinone-9 in Green Algae and Higher Plants

Lichtenthaler, H. K., Rohmer, M., Schwender, J., Disch, A., & Seemann, M. (1997) · Springer eBooks · doi:10.1007/978-94-017-2662-7_56 · Cited by 6

Evolutionary Integration of Chloroplast Metabolism with the Metabolic Networks of the Cells

Linka, M., & Weber, A. P. M. (2011) · Advances in photosynthesis and respiration · doi:10.1007/978-94-007-1533-2_8 · Cited by 5

A new alternative non-mevalonate pathway for isoprenoid biosynthesis in eubacteria and plants.

Paseshnichenko, V. A. (1998) · PubMed · Cited by 27

Distribution of the mevalonate and glyceraldehyde phosphate/pyruvate pathways for isoprenoid biosynthesis in unicellular algae and the cyanobacterium Synechocystis PCC 6714

Disch, A., Schwender, J., Müller, C. R., Lichtenthaler, H. K., & Rohmer, M. (1998) · Biochemical Journal · doi:10.1042/bj3330381 · Cited by 217

Investigations on the isoprenoid biosynthesis in the green alga Scenedesmus obliquus by using the "1"3C-labelling technique

Schwender, J. (1995) · OpenGrey (Institut de l'Information Scientifique et Technique)

The non-mevalonate isoprenoid biosynthesis and its distribution in plants

Schwender, J. (1999) · OpenGrey (Institut de l'Information Scientifique et Technique)

Two independent biochemical pathways for isopentenyl diphosphate and isoprenoid biosynthesis in higher plants

Lichtenthaler, H. K., Rohmer, M., & Schwender, J. (1997) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1997.tb01049.x · Cited by 473