scholarly journals First report on the swim bladder index, proximate composition, and fatty acid analysis of swim bladder from cultured Totoaba macdonaldi fed compound aquafeeds

2021 ◽  
Vol 21 ◽  
pp. 100901
Author(s):  
Mayra L. González-Félix ◽  
Martin Perez-Velazquez ◽  
Miguel Castellanos-Rico ◽  
Adam M. Sachs ◽  
Laura D. Gray ◽  
...  
Plant Disease ◽  
2008 ◽  
Vol 92 (2) ◽  
pp. 315-315 ◽  
Author(s):  
K. A. Wise ◽  
Y. F. Zhao ◽  
C. A. Bradley

In 2006, a seed lot of dry pea cv. DS Admiral obtained from Bowman County, North Dakota contained seed with bright-to-pale pink discoloration on the seed coat. Five discolored seeds and five seeds with normal appearance were surface disinfected in a 0.5% NaOCl solution for 1 min and rinsed with sterilized distilled water for 1 min. Seeds were placed onto potato dextrose agar (PDA) and incubated at 22°C. Three days later, the discolored seeds produced pink bacterial colonies and a pink pigment that diffused throughout the PDA. The pink bacterial colonies were tentatively identified as Erwinia rhapontici on the basis of colony and pigment color (2,3). No fungi or bacteria grew from the seed with normal appearance. A pink bacterial colony growing from one of the discolored seeds was streaked onto PDA and a single colony was obtained. A streaked plate incubated at 37°C showed no growth, which distinguishes E. rhapontici from Brenneria rubrifaciens (formerly E. rubrifaciens) (1–3). To confirm the identity, the isolate was sent to the Bacterial Identification and Fatty Acid Analysis Laboratory at the University of Florida, Gainesville. Fatty acid analysis indicated a similarity index of 0.515 for E. rhapontici. For an additional confirmation of identity, the 16S ribosomal DNA (rDNA) gene was amplified from the E. rhapontici isolate with universal primers fD1 and rP1 (4). The PCR product was cloned into pGEM-T easy vector (Promega, Madison, WI) and sequenced with primers SP6 and T7 at the Keck Biotechnology Center at the University of Illinois, Urbana. The resulting nucleotide sequence was compared with 16S rDNA sequences deposited in the ribosomal database ( http://rdp.cme.msu.edu/seqmatch/seqmatch_intro.jsp ) and showed highest identity to sequences of E. rhapontici or E. persicinus strains. To confirm pathogenicity, the basal ends of five pods on each of six pea plants (cv. Carneval) were syringe injected with 0.1 ml of suspension containing the obtained E. rhapontici isolate in the greenhouse by the methods as previously described (2). As a control, five pods on each of two plants were injected with 0.1 ml of sterile distilled water. Twenty-eight of the 51 seeds obtained from the bacteria-inoculated pods had pink seed symptoms, while seeds from the control pods appeared normal. Isolations from symptomatic and asymptomatic seed were performed as described above, and E. rhapontici was obtained from symptomatic seed. To our knowledge, this is the first report of pink seed of pea caused by E. rhapontici in North Dakota. The first report of this disease on pea in the United States was from Montana (3). References: (1) L. Hauben et al. Syst. Appl. Microbiol. 21:384, 1998. (2) H. C. Huang et al. Can. J. Plant Pathol. 12:445, 1990. (3) B. K. Schroeder et al. Plant Dis. 86:188, 2002. (4) W. G. Weisburg et al. J. Bacteriol. 173:697, 1991.


Plant Disease ◽  
1997 ◽  
Vol 81 (9) ◽  
pp. 1096-1096 ◽  
Author(s):  
R. D. Gitaitis ◽  
J. D. Gay

In May 1997, sweet onions (Allium cepa L.) grown in Toombs County, GA, displayed symptoms of blighted leaves, bleached and rotted seed stalks, and rotted bulbs. Gram-negative bacteria were isolated from infected tissues on nutrient agar and shown to be from the genus Pantoea on the basis of cell morphology (rod-shaped), yellow pigmentation, utilization of glucose in an oxidative and fermentative manner, presence of catalase, and absence of oxidase. These characteristics are typical of bacterial strains belonging to the Enterobacteriaceae (facultative anaerobes). Initially, these bacteria were thought to be P. agglomerans, a common saprophyte associated with plant material. However, fatty acid analysis, using bacterial identification software (MIDI, Dewark, DE), identified (second choice) some strains as possibly being P. ananas.. Further testing indicated that all strains utilized cellobiose, melibiose, inositol, glycerol, and sucrose, but not pectin, starch, or gelatin. However, those strains identified by fatty acid analysis as P. ananas were differentiated from P. agglomerans on the basis of indole production, lack of phenylalanine deaminase, and lack of nitrate reductase. To confirm pathogenicity, three strains of each species (total of six strains) were grown overnight in nutrient broth shake cultures. Bacterial cells were harvested by centrifugation and suspended in 0.01 M phosphate-buffered saline (0.85%). Inoculum was adjusted to approximately 5 × 108 CFU/ml with a spectrophotometer and misted with a chromatography sprayer onto onion leaves of approximately 10-week-old onion plants in the greenhouse. Onions were predisposed by placing them under plastic bags for 18 h prior to inoculation. Inoculated plants were left covered with plastic bags for an additional 24 h after inoculation. There were two plants per pot, each test had three pots, and the test was conducted twice. The three strains of P. agglomerans and buffer control resulted in no symptoms. The three strains of P. ananas produced severe blighting, rapid collapse of tissues, and rapid drying so that leaves were light tan and dry within 3 days. Disease on plants infected with P. ananas continued to develop until death of all foliage and bulbs shriveled and collapsed. Results were consistent for all replications and both trials. Bacteria recovered from diseased tissues were gram-negative, yellow, and facultative anaerobic, and produced indole but not phenylalanine deaminase or nitrate reductase; i.e., the bacteria demonstrated the same characteristics as P. ananas. Although P. agglomerans has been reported to produce similar symptoms in South Africa (1), our P. agglomerans strains were nonpathogenic. To our knowledge this is the first report of P. ananas causing a disease of onion. Reference: (1) M. J. Hattingh and D. F. Walters Plant Dis. 65:615, 1981.


2017 ◽  
Vol 4 (04) ◽  
Author(s):  
SUNITA SINGH ◽  
R. P. SINGH ◽  
H. K. SINGH ◽  
N. A. KHAN ◽  
M. K. MAURYA

Among the oilseed Brassica crops, Indian mustard [Brassica juncea (L.) Czern and Coss.] is an important source of oil from a nutritional point of view. The nutritional value of oil and cake quality is governed mainly by the composition of its fatty acids, iodine value, saponification, acid value, glucosinolates, crude fibre, protein and limiting amino acids, etc. Seventeen varieties/strains of Indian mustard were taken for saturated and unsaturated fatty acid analysis. The eicosenoic was absent in genotype (NUDBYJ-10) and erucic acid (NUDBYJ-10, LES-46 and Pusa mustard- 21). The fatty acid composition found a variable in different genotypes. Saturated fatty acid, Palmitic + Stearic ranged between 2.3 to 6.5%, Oleic 10.6 to 40.7%, Linoleic 16.1 to 37.7%, Linolenic 13.3 to 26.7%, Eicosenoic 0.00 to 10.30% and Erucic acid 0.00 to 47.50%, respectively. Alternaria blight severity also varied in different genotypes and ranged between 18.75 to 56.25%, maximum being in genotype Kranti and minimum in LES-47. No significant correlation was observed between the fatty acid composition and disease severity. The oil content range from 38.1 to 42.60% and protein content was found highest in variety RGN-73. The amino acid viz. methionine and tryptophan range between 0.41 to 1.81 g/16gN and 0.41 to 1.81 g /16g N, respectively.


Author(s):  
Souta AOMORI ◽  
Megumu FUJIABAYASHI ◽  
Kunihiro OKANO ◽  
Yoshihiro TAKADA ◽  
Naoyuki MIYATA

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