The mechanistic basis for differential sensitivities to chilling‐induced photoinhibition among two rice (Oryza sativa L.) cultivars (an Indica and a Japonica type) and one barley cultivar (Hordeum vulgare L. cv. Albori) was examined. When leaf segments were exposed to moderate illumination at 4°C, a sustained decrease in the photochemical efficiency of photosystem (PS) II measured as the ratio of variable to maximal fluorescence (Fv/Fm) was observed for several hours. An analysis of fluorescence quenching revealed a sudden drop in PSII‐driven electron transport rate (ETR) and a rapid rise in the reduction state of the primary electron acceptor QA upon exposure to chilling in moderate light. There was no appreciable difference in the level of non‐photochemical quenching (NPQ) nor in the xanthophyll cycle activity between Japonica rice and barley. However, barley was capable of sustaining a higher ETR, thereby keeping a lower reduction state of QA throughout the chilling for 6 h. The Indica rice was characterized by the lowest ability to develop the xanthophyll cycle‐associated NPQ, particularly the fast relaxing NPQ component (qf), accompanied by the highest reduction state of QA and photoinhibitory quenching (qI). It is concluded that the lower susceptibility of barley to chilling‐induced photoinhibition than Japonica rice is attributable to its higher potential to dissipate excess light energy via a photochemical mechanism, whereas Indica rice is more sensitive to photoinhibition at a chilling temperature than Japonica rice, due primarily to its lower capacity to develop an efficient NPQ pathway.
This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Tomato was considered as one of the most widely cultivated vegetable crops in the world. Tomato plant has high antioxidant capacity which can be attributed to the high levels of carotenoids, phenols, vitamins C and E. However, most of tomato plants have been discarded as waste after fruit harvesting. In order to identify genetic resources with high antioxidant level for use in food or as feed additives, we investigated the ABTS, DPPH antioxidant activity and polyphenol content in tomato leaves and stems. A total of 112 tomato accessions were classified into three groups by latitude of their collected countries: 30°~60° North (50 accessions), 0°~30° North (40 accessions), and 0°~30° South (22 accessions). Stem and leaf extracts showed wide variation in ABTS antioxidant activity ranging from 1.6 ± 1.0 to 48.4 ± 6.1 μg Trolox mg -1 dw. The antioxidant activity of DPPH was in the range of 6.3 ± 0.2 to 40.0 ± 0.3 μg ASC mg -1 dw. Total polyphenol content ranged from 6.1 ± 0.2 to 38.9 ± 0.7 μg GAE mg -1 dw. ABTS, DPPH antioxidant activities and polyphenol content in accessions from 30°~60°N latitude were significantly higher (P<0.05) than those from 0°~30°N latitude. ABTS values showed a significant positive correlation (r = 0.700**) with DPPH activity. IT100506 (KOR) and 702959 (UKR) were recommended as potential sources of natural antioxidants due to their highest antioxidant activity among accessions. This study will provide valuable information for tomato breeders in developing and producing functional food or feed additives resources.
Taxonomic position of 46 Korean isolates of Rhizoctonia solani which were classified into nine intraspecific groups by anastomosis and cultural characteristics was analyzed by randomly amplified polymorphic DNA (RAPD) and sequence analyses of the internal transcribed spacer (ITS) regions of ribosomal DNA. All the isolates within each group showed highly similar band patterns in RAPD. The ITS regions of the isolates within the same groups showed a high level of sequence similarity above 96.0% whereas similarities among different groups were below 94.4%. When compared with several reference strains of R. solani from foreign countries, all the Korean isolates were clustered with the foreign isolates belonging to the same groups in the phylogenetic tree. All six Korean strains of AG-4 were identified as HG-1 out of 3 subgroup of AG-4. We discussed taxonomic position of Korean isolates of R. solani and showed that sequence analysis with ITS regions could be a rapid and useful method for identification of intraspecific group of R. solani.
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