Pyridine nucleotide cycle and trigonelline (N‐methylnicotinic acid) synthesis in developing leaves and fruits of Coffea arabica

Physiologia Plantarum - Tập 122 Số 4 - Trang 404-411 - 2004
Xin‐Qiang Zheng1, Chifumi Nagai2, Hiroshi Ashihara1,3
1Department of Advanced Biosciences, Graduate Division of Human Environmental Science, Graduate School of Humanities and Sciences, Ochanomizu University, Bunkyo-ku, Tokyo 112-8610, Japan
2Hawaii Agriculture Research Center, Aiea, Hawaii 96701-3911, USA
3Metabolic Biology Group, Department of Biology, Faculty of Science, Ochanomizu University, Bunkyo-ku, Tokyo 112-8610, Japan

Tóm tắt

We examined the biosynthesis of trigonelline in leaves and fruits of Arabica coffee (Coffea arabica) plants. [3H]Quinolinic acid, which is an intermediate of de novo pyridine nucleotide synthesis, and [14C]nicotinamide and [14C]nicotinic acid, which are degradation products of NAD, were converted to trigonelline and pyridine nucleotides. These tracer experiments suggest that the pyridine nucleotide cycle, nicotinamide → nicotinic acid → nicotinic acid mononucleotide (NaMN) → nicotinic acid adenine dinucleotide (NaAD) → NAD → nicotinamide mononucleotide (NMN) → nicotinamide, operates in coffee plants, and trigonelline is synthesized from nicotinic acid formed in the cycle. Trigonelline accumulated up to 18 µmol per leaf in developed young leaves, and then decreased with age. Although the biosynthetic activity of trigonelline from exogenously supplied [14C]nicotinamide was observed in aged leaves, the endogenous supply of nicotinamide may be limited, reducing the contents in these leaves. Trigonelline is synthesized and accumulated in fruits during development. The trigonelline synthesis in pericarps is much higher than that in seeds, but its content in seeds is higher than pericaps, so that some of the trigonelline synthesized in the pericarps may be transported to seeds. Trigonelline in seeds may be utilized during germination, as its content decreases. Trigonelline synthesis from [14C]nicotinamide was also found in Theobroma cacao plants, but instead of trigonelline, nicotinic acid‐glucoside was synthesized from [14C]nicotinamide in Camellia sinensis plants.

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Tài liệu tham khảo

10.1034/j.1399-3054.2000.108001025.x

10.1007/978-3-642-70717-9_18

10.1007/BF00386502

10.1007/978-1-4615-6657-1_5

10.1007/978-1-4615-6657-1_13

Frost GM, 1967, Nicotinamide adenine dinucleotide as a precursor of nicotine in Nicotiana rustica L, J Biol Chem, 242, 887, 10.1016/S0021-9258(18)96207-1

10.1038/212933a0

10.1002/cber.188501802144

10.1016/S0021-9258(18)64575-2

10.2741/1350

10.1104/pp.53.4.603

10.1016/0031-9422(91)83637-Z

Moat AG, 1987, Pyridine Nucleotide Coenzymes. Chemical, Biochemical, and Medical Aspects, Part B., 1

Poulton JE, 1981, The Biochemistry of Plants, 667

10.1055/s-2000-16645

10.1271/bbb1961.49.3467

10.1271/nogeikagaku1924.61.183

10.1016/0006-291X(83)91763-1

10.1016/0003-9861(88)90396-7

10.1007/BF00391419

10.1007/BF00392369

10.1007/BF00398100

Waller GR, 1966, The pyridine nucleotide cycle and its role in the biosynthesis of ricinine by Ricinus communis L, J Biol Chem, 241, 4411, 10.1016/S0021-9258(18)99736-X

10.1016/S0031-9422(00)90924-5

10.1016/j.plantsci.2003.11.024