𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cypridina bioluminescence—VII : The bioluminescence of Cypridina luciferin analogs

✍ Scribed by T. Goto; M. Isobe; D.A. Coviello; Y. Kishi; S. Inoue


Publisher
Elsevier Science
Year
1973
Tongue
French
Weight
487 KB
Volume
29
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Cypridina bioluminescence I Sructure of
✍ Toshito Kishi; Toshio Goto; Yoshimasa Hirata; Osamu Shimomura; Frank H. Johnson 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 421 KB

BIOLlEilNlSCENCE of Cypridina hilgendorfii (Japenese name:umi-hotaru) has been studied extensively since 1917, when Harvey (1) observed the luciferin-luciferase reaction with extracts of this animal. The luminescent system of Cypridina is one of the simplest among luminous animals and plantc 60 far

Cypridina bioluminescence III total synt
✍ Yoshito Kishi; Toshio Goto; Shoji Inoue; Sumi Sugiura; Hisako Kishimoto 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 213 KB

CYPRIDINA luciferin (I) has been shoosn to have the structure represented by Ia (1). We wish to report in this oommunioation a total.

Cypridina bioluminescence VI a new route
✍ S. Inoue; S. Sugiura; H. Kakoi; T. Goto 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 106 KB

A total synthesis of Cypridina luciferin (I), a bioluminescent substance obtained from Cypridina hilgendorfii (l), was achieved in 1966 (2) by reductive condensation of an appropriate 2-aminopyrazine derivative and a-keto acid, but the yield was too low to use th!s route for preparative purposes. Tw

Cypridina bioluminescence VII. chemilumi
✍ Toshio Goto; Hiroshi Fukatsu 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 232 KB

Cypridina bioluminescence is produced in aqueous solution by oxidation of Cypridina luciferin (substrate) with molecular oxygen in the presence of Cypridina luciferase (enzyme), which may be classified as one of the dioxygenases (1). Luciferin also chemiluminesces strongly in aprotic solvents such a

Cypridina bioluminescence II structural
✍ Yoshito Kishi; Toshio Goto; Shoji Eguchi; Yoshimasa Hirata; Eiji Watanabe; Tetsu 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 270 KB

STRCCTlJR.R of Cypridina luciferin (I) 'RLE elucidated as described in the preceding oonnaunication (1). During this investigation, snalysis of the high-resolution mass spectra of some derivatives of luciferin greatly contributed for determination not only of the molecular formula of luciferin but