Acrolein, an α,β-Unsaturated Carbonyl, Inhibits Both Growth and PSII Activity in the Cyanobacterium Synechocystis sp PCC 6803

被引:18
作者
Shimakawa, Ginga [1 ]
Iwamoto, Tatsuya [1 ]
Mabuchi, Tomohito [1 ]
Saito, Ryota [1 ]
Yamamoto, Hiroshi [2 ]
Amako, Katsumi [3 ]
Sugimoto, Toshio [1 ]
Makino, Amane [4 ,5 ]
Miyake, Chikahiro [1 ,5 ]
机构
[1] Kobe Univ, Grad Sch Agr Sci, Fac Agr,Dept Biol & Environm Sci, Nada Ku, Kobe, Hyogo 6578501, Japan
[2] Kyoto Univ, Grad Sch Sci, Dept Bot, Sakyo Ku, Kyoto 6068502, Japan
[3] Kobe Gakuin Univ, Fac Nutr, Nishi Ku, Kobe, Hyogo 6512180, Japan
[4] Tohoku Univ, Grad Sch Agr Sci, Dept Agr, Aoba Ku, Sendai, Miyagi 9818555, Japan
[5] JST, CREST, Chiyoda Ku, Tokyo 1020076, Japan
基金
日本学术振兴会;
关键词
acrolein; NADPH-dependent acrolein reduction (NAR); photosynthesis; plant diabetes; reactive carbonyls (RCs); ALDO-KETO REDUCTASES; LIPID-PEROXIDATION; PHOTOSYSTEM-I; PROTEIN CARBONYLATION; ARABIDOPSIS-THALIANA; OXIDATIVE STRESS; DETOXIFICATION; METHYLGLYOXAL; IDENTIFICATION; DEHYDROGENASE;
D O I
10.1271/bbb.130186
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we sought to determine whether and how an alpha,beta-unsaturated carbonyl, acrolein, can inhibit the growth of the cyanobacterium Synechocystis sp. PCC6803 (S. 6803). Treatment of S. 6803 with 200 mu M acrolein for 3 d significantly and irreversibly inhibited its growth. To elucidate the inhibitory mechanism, we examined the effects of acrolein on photosynthesis. In contrast to dark conditions, the addition of acrolein to S. 6803 under conditions of illumination lowered the CO2-dependent O-2 evolution rate (photosynthetic activity). Furthermore, treatment with acrolein lowered the activity reducing dimethyl benzoquinone in photosystem II (PSII). Acrolein also suppressed the reduction rate for the oxidized form of the reaction center chlorophyll of photosystem I (PSI), P700. These results indicate that acrolein inhibited PSII activity in thylakoid membranes. The addition of 200 mu M acrolein to the illuminated S. 6803 cells gradually increased the steady-state level (Fs) of Chl fluorescence and decreased the quantum yield of PSII. These results suggested that acrolein damaged the acceptor side of PSII. On the other hand, acrolein did not inhibit respiration. From the above results, we gained insight into the metabolism of acrolein and its physiological effects in S. 6803.
引用
收藏
页码:1655 / 1660
页数:6
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