40
S. Takaichi
Steinbrenner, J., & Linden, H. (2001). Regulation of two carotenoid biosynthesis genes coding for
phytoene synthase and carotenoid hydroxylase during stress-induced astaxanthin formation in
the green alga Haematococcus pluvialis. Plant Physiology, 125, 810–817.
Steinbrenner, J., & Linden, H. (2003). Light induction of carotenoid biosynthesis genes in the
green alga Haematococcus pluvialis: regulation by photosynthetic redox control. Plant Molecular
Biology, 52, 343–356.
Stickforth, P., Steiger, S., Hess, W. R., & Sandmann, G. (2003). A novel type of lycopene ε-cyclase
in the marine cyanobacterium Prochlorococcus marinus MED4. Archives of Microbiology, 179,
409–415.
Sugiyama, K., & Takaichi, S. (2020). Carotenogenesis in cyanobacteria: CruA/CruP-type and CrtLtype lycopene cyclases. The Journal of General and Applied Microbiology, 66, 53–58.
Sugiyama, K., Ebisawa, M., Yamada, M., Nagashima, Y., Suzuki, H., Maoka, T., et al. (2017).
Functional lycopene cyclase (CruA) in cyanobacterium, Arthrospira platensis NIES-39, and its
role in carotenoid synthesis. Plant and Cell Physiology, 58, 831–838.
Sugiyama, K., Takahashi, K., Nakazwa, K., Yamada, M., Kato, S., Shinomura, T., Nagashima, Y.,
Suzuki, H., Ara, T., Harada, J., & Takaichi, S. (2020). Oxygenic phototrophs need ζ-carotene
isomerase (Z-ISO) for carotene synthesis: functional analysis in Arthrospira and Euglena. Plant
and Cell Physiology, 61, 276–282.
Swift, I. E., & Milborrow, B. V. (1981). Stereochemistry of allene biosynthesis and the formation
of the acetylenic carotenoid diadinoxanthin and peridinin (C 37 ) from neoxanthin. Biochemical
Journal, 199, 69–74.
Swift, I. E., Milborrow, B. V., & Jeffrey, S. W. (1982). Formation of neoxanthin, diadinoxanthin and peridinin from [ 14 C]zeaxanthin by a cell-free system from Amphidinium carterae.
Phytochemistry, 21, 2859–2864.
Takaichi, S. (2000). Characterization of carotenes in a combination of a C18 HPLC column
with isocratic elution and absorption spectra with a photodiode-array detector. Photosynthesis
Research, 65, 93–99.
Takaichi, S. (2009). Distribution and biosynthesis of carotenoids. In C. N. Hunter, F. Daldal, M. C.
Thurnauer, & J. T. Beatty (Eds.), The purple phototrophic bacteria (pp. 97–117). Dordrecht, The
Netherlands: Springer.
Takaichi, S. (2011). Carotenoids in algae: distributions, biosynthesis and functions. Marine Drugs,
9, 1101–1118.
Takaichi, S. (2014). General methods for identification of carotenoids. Biotechnology Letters, 36,
1127–1128.
Takaichi, S., & Maoka, T. (2015). Identification and spectroscopic characterization of neurosporene.
Biotechnology Letters, 37, 2027–2031.
Takaichi, S., & Mimuro, M. (1998). Distribution and geometric isomerism of neoxanthin in oxygenic
phototrophs: 9 -cis, a sole molecular form. Plant and Cell Physiology, 39, 968–977.
Takaichi, S., & Mochimaru, M. (2007). Carotenoids and carotenogenesis in cyanobacteria: unique
ketocarotenoids and carotenoid glycosides. Cellular and Molecular Life Sciences, 64, 2607–2619.
Takaichi, S., & Shimada, K. (1992). Characterization of carotenoids in photosynthetic bacteria.
Methods in Enzymology, 213, 374–385.
Takaichi, S., Shimada, K., & Ishidsu, J. (1990). Carotenoids from the aerobic photosynthetic bacterium, Erythrobactor longus: β-carotene and its hydroxyl derivatives. Archives of
Miclobiology, 153, 118–122.
Takaichi, S., Maoka, T., & Masamoto, K. (2001). Myxoxanthophyll in Synechocystis sp. PCC 6803 is
myxol 2 -dimethyl-fucoside, (3R,2 S)-myxol 2 -(2,4-di-O-methyl-α-l-fucoside), not rhamnoside.
Plant and Cell Physiology, 42, 756–762.
Takaichi, S., Mochimaru, M., Uchida, H., Murakami, A., Hirose, E., Maoka, T., et al. (2012). Opposite chilarity of α-carotene in unusual cyanobacteria with unique chlorophylls, Acaryochloris and
Prochlorococcus. Plant and Cell Physiology, 53, 1881–1888.
Takaichi, S., Yokoyama, A., Mochimaru, M., Uchida, H., & Murakami, A. (2016). Carotenogenesis
diversification in pholygenetic lineages of Rhodophyta. Journal of Phycology, 52, 329–338.
S. Takaichi
Steinbrenner, J., & Linden, H. (2001). Regulation of two carotenoid biosynthesis genes coding for
phytoene synthase and carotenoid hydroxylase during stress-induced astaxanthin formation in
the green alga Haematococcus pluvialis. Plant Physiology, 125, 810–817.
Steinbrenner, J., & Linden, H. (2003). Light induction of carotenoid biosynthesis genes in the
green alga Haematococcus pluvialis: regulation by photosynthetic redox control. Plant Molecular
Biology, 52, 343–356.
Stickforth, P., Steiger, S., Hess, W. R., & Sandmann, G. (2003). A novel type of lycopene ε-cyclase
in the marine cyanobacterium Prochlorococcus marinus MED4. Archives of Microbiology, 179,
409–415.
Sugiyama, K., & Takaichi, S. (2020). Carotenogenesis in cyanobacteria: CruA/CruP-type and CrtLtype lycopene cyclases. The Journal of General and Applied Microbiology, 66, 53–58.
Sugiyama, K., Ebisawa, M., Yamada, M., Nagashima, Y., Suzuki, H., Maoka, T., et al. (2017).
Functional lycopene cyclase (CruA) in cyanobacterium, Arthrospira platensis NIES-39, and its
role in carotenoid synthesis. Plant and Cell Physiology, 58, 831–838.
Sugiyama, K., Takahashi, K., Nakazwa, K., Yamada, M., Kato, S., Shinomura, T., Nagashima, Y.,
Suzuki, H., Ara, T., Harada, J., & Takaichi, S. (2020). Oxygenic phototrophs need ζ-carotene
isomerase (Z-ISO) for carotene synthesis: functional analysis in Arthrospira and Euglena. Plant
and Cell Physiology, 61, 276–282.
Swift, I. E., & Milborrow, B. V. (1981). Stereochemistry of allene biosynthesis and the formation
of the acetylenic carotenoid diadinoxanthin and peridinin (C 37 ) from neoxanthin. Biochemical
Journal, 199, 69–74.
Swift, I. E., Milborrow, B. V., & Jeffrey, S. W. (1982). Formation of neoxanthin, diadinoxanthin and peridinin from [ 14 C]zeaxanthin by a cell-free system from Amphidinium carterae.
Phytochemistry, 21, 2859–2864.
Takaichi, S. (2000). Characterization of carotenes in a combination of a C18 HPLC column
with isocratic elution and absorption spectra with a photodiode-array detector. Photosynthesis
Research, 65, 93–99.
Takaichi, S. (2009). Distribution and biosynthesis of carotenoids. In C. N. Hunter, F. Daldal, M. C.
Thurnauer, & J. T. Beatty (Eds.), The purple phototrophic bacteria (pp. 97–117). Dordrecht, The
Netherlands: Springer.
Takaichi, S. (2011). Carotenoids in algae: distributions, biosynthesis and functions. Marine Drugs,
9, 1101–1118.
Takaichi, S. (2014). General methods for identification of carotenoids. Biotechnology Letters, 36,
1127–1128.
Takaichi, S., & Maoka, T. (2015). Identification and spectroscopic characterization of neurosporene.
Biotechnology Letters, 37, 2027–2031.
Takaichi, S., & Mimuro, M. (1998). Distribution and geometric isomerism of neoxanthin in oxygenic
phototrophs: 9 -cis, a sole molecular form. Plant and Cell Physiology, 39, 968–977.
Takaichi, S., & Mochimaru, M. (2007). Carotenoids and carotenogenesis in cyanobacteria: unique
ketocarotenoids and carotenoid glycosides. Cellular and Molecular Life Sciences, 64, 2607–2619.
Takaichi, S., & Shimada, K. (1992). Characterization of carotenoids in photosynthetic bacteria.
Methods in Enzymology, 213, 374–385.
Takaichi, S., Shimada, K., & Ishidsu, J. (1990). Carotenoids from the aerobic photosynthetic bacterium, Erythrobactor longus: β-carotene and its hydroxyl derivatives. Archives of
Miclobiology, 153, 118–122.
Takaichi, S., Maoka, T., & Masamoto, K. (2001). Myxoxanthophyll in Synechocystis sp. PCC 6803 is
myxol 2 -dimethyl-fucoside, (3R,2 S)-myxol 2 -(2,4-di-O-methyl-α-l-fucoside), not rhamnoside.
Plant and Cell Physiology, 42, 756–762.
Takaichi, S., Mochimaru, M., Uchida, H., Murakami, A., Hirose, E., Maoka, T., et al. (2012). Opposite chilarity of α-carotene in unusual cyanobacteria with unique chlorophylls, Acaryochloris and
Prochlorococcus. Plant and Cell Physiology, 53, 1881–1888.
Takaichi, S., Yokoyama, A., Mochimaru, M., Uchida, H., & Murakami, A. (2016). Carotenogenesis
diversification in pholygenetic lineages of Rhodophyta. Journal of Phycology, 52, 329–338.