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1.
Plant Dis ; 100(5): 996-1006, 2016 May.
Article in English | MEDLINE | ID: mdl-30686149

ABSTRACT

Anthracnose caused by Colletotrichum spp. is a serious disease of strawberry. The etiology of anthracnose of strawberry is complex, and several Colletotrichum spp. have been regarded as causal agents. In the present study, multilocus (actin, ß-tubulin, calmodulin, glyceraldehyde-3-phosphate dehydrogenase, and chitin synthase) phylogenetic analysis revealed that 100 isolates of Colletotrichum associated with anthracnose of strawberry in central China belong to five species. In total, 97 isolates were identified belonging to the Colletotrichum gloeosporioides species complex, with C. murrayae, C. gloeosporioides, C. fructicola, and C. aenigma accounting for 81, 8, 4, and 4% of the total isolates, respectively. Three isolates belonging to the C. acutatum complex were identified as C. nymphaeae. On inoculated strawberry plants, isolates of C. fructicola and C. murrayae species showed strong pathogenicity to both leaves and petioles of strawberry, with plant mortality 30 days after inoculation of 77.8 and 55.6%, respectively. C. gloeosporioides, C. aenigma, and C. nymphaeae showed strong pathogenicity to leaves but weak pathogenicity to petioles, with plant mortality 30 days after inoculation of 5.6, 16.7, and 11.1%, respectively. The five species were divided into four classes based on their maximum growth temperatures. Isolates of C. murrayae and C. gloeosporioides were more tolerant to high temperature (>34°C) than isolates of other species, followed by C. fructicola and C. aenigma. Isolates of C. nymphaeae, which are only distributed in areas of higher altitude (1,100 m), were highly sensitive to higher temperature. These results indicate that pathogenicity and adaptation to temperature are important factors in the distribution of Colletotrichum spp. on strawberry plants. This research may increase our understanding of how Colletotrichum spp. emerge and spread to geographical regions with different latitudes or elevations.

2.
Asian-Australas J Anim Sci ; 25(12): 1734-41, 2012 Dec.
Article in English | MEDLINE | ID: mdl-25049539

ABSTRACT

This trial was performed to study the effects of replacing soybean meal (SBM) with fermented rapeseed meal (RSM) on growth performance, serum biochemistry variable and intestinal morphology of broilers. A total of 640 d-old Arbor Acres broiler chicks were randomly allocated to 4 dietary treatments, 4 pens per treatment and 40 birds per pen for a 6-wk feeding trial. In the four treatment groups, fermented RSM replaced soybean meal at 0, 5, 10, and 15%, respectively. On 21 d and 42 d, two birds from each pen were randomly selected and slaughtered. Blood samples and sections of duodenum, jejunum, and ileum were collected for measurement of serum biochemical variables and intestinal morphology, respectively. Results showed that body weight gain (BWG) and feed conversion (FC) were significantly (p<0.01) poorer for birds fed the 15% fermented RSM diet than those fed with 0, 5 and 10% fermented RSM diets during all periods. Compared with 0 and 5% fermented RSM groups, IgG content in the serum of birds in 10 and 15% fermented RSM groups was improved (p<0.01) urea nitrogen content of serum was reduced (p<0.01) during both growing and finishing periods. However, IgM, phosphorus and calcium levels increased (p<0.05) only during the growing period. Increased (p<0.05) villus height was observed in the duodenum and jejunum of broilers fed the diet with 10% fermented RSM. In addition, villus height to crypt depth ratio in the jejunum was significantly higher (p<0.01) for birds fed the diet with 10% fermented RSM than for those fed diets with 0, 5 and 15% fermented RSM. The present results suggest that RSM fermented with Lactobacillus fermentum and Bacillus subtilis is a promising alternative protein source and that it could be safely used replace up to 10% SBM in broiler diets.

3.
Biochim Biophys Acta ; 1545(1-2): 6-12, 2001 Feb 09.
Article in English | MEDLINE | ID: mdl-11342026

ABSTRACT

The Tsou method was used to study the kinetic course of inactivation of green crab alkaline phosphatase by zinc ions. The results show that the enzyme was inactivated by a complexing scheme which has not been previously identified. The enzyme first reversibly and quickly binds Zn(2+) and then undergoes a slow reversible course to inactivation and slow conformational change. The inactivation reaction is a single molecule reaction and the apparent inactivation rate constant is for a saturated reaction being independent of Zn(2+) concentration if the concentration is sufficiently high. The microscopic rate constants of inactivation and the association constant were determined from the measurements.


Subject(s)
Alkaline Phosphatase/antagonists & inhibitors , Brachyura/enzymology , Enzyme Inhibitors/pharmacology , Zinc Acetate/pharmacology , Alkaline Phosphatase/chemistry , Aniline Compounds/pharmacology , Animals , Dose-Response Relationship, Drug , Kinetics , Organophosphorus Compounds/pharmacology , Protein Conformation/drug effects
4.
Hua Xi Yi Ke Da Xue Xue Bao ; 20(1): 96-8, 1989 Mar.
Article in Chinese | MEDLINE | ID: mdl-2793154

ABSTRACT

In this paper, the early passage diploid Syrian hamster embryo (SHE) cells were used as the source of target. Four chemicals were appraised in SHE transformation test to determine whether they were carcinogens or not. They were (1) 2-benzoyl-hydrazono-1,3-diethiolane(BHD) (technical product); (2) isoprothiolane (pure product); (3) isoprothiolane (technical product); (4) benzene-abstracts from coal smoke of coke oven (benzene-abstracts). The results showed that morphological transformation was not observed when cells were not treated or treated with dimethyl sulfoxide, BHD, pure isoprothiolane and the technical product of isoprothiolane. The highest concentration had considerable cytotoxicity. In the groups of positive control (1.0 microgram/ml 3-methyl-cholanthrene, 10.0 micrograms/ml benzo (a) pyrene) and benzene-abstracts, we could observe colonies with random or criss-cross orientation and dense piling-up of cells. According to well known positive criteria, the benzene-abstracts can induce SHE cells morphological transformation. The other three chemicals can not induce SHE cells transformation.


Subject(s)
Benzene/toxicity , Cell Transformation, Neoplastic/drug effects , Fungicides, Industrial/toxicity , Hydrazones/toxicity , Smoke/analysis , Thiophenes/toxicity , Animals , Cells, Cultured , Coal , Cricetinae , Embryo, Mammalian , Mesocricetus
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