scholarly journals Quality of fermented goat milk with carrot juice during cold storage

2021 ◽  
Vol 694 (1) ◽  
pp. 012076
Author(s):  
Y F Kurnia ◽  
E L S Suharto ◽  
E Purwati
Keyword(s):  
2013 ◽  
Vol 113 (1) ◽  
pp. 205-210 ◽  
Author(s):  
Anderson Keizo Yamazi ◽  
Thalita Scatamburlo Moreira ◽  
Valéria Quintana Cavicchioli ◽  
Raquel Cristina Konrad Burin ◽  
Luís Augusto Nero

2009 ◽  
Vol 70 (1) ◽  
pp. 135-144 ◽  
Author(s):  
Marek Gajewski ◽  
Zenon Węglarz ◽  
Anna Sereda ◽  
Marta Bajer ◽  
Agnieszka Kuczkowska ◽  
...  

Quality of Carrots Grown for Processing as Affected by Nitrogen Fertilization and Harvest TermIn 2007-2008 the effect of nitrogen fertilization and harvest term on quality of two carrot cultivars was investigated. The field experiment was carried out in Żelazna Experimental Station of Warsaw University of Life Sciences. Karotan F1and Trafford F1cultivars, commonly grown for juice industry, were the objects of the experiment. Carrot seeds were sown at the beginning of May. Nitrogen fertilization was applied in five rates, ranged from 0 to 120 kg·ha-1and in two terms — before sowing and in the middle of growing season. Roots were harvested in three terms: mid-September, mid-October and the first decade of November. After harvest there were determined: nitrates (NO3) content in carrot roots and juice, soluble solids, colour parameters of juice in CIE L*a*b*system. The dose and the term of nitrogen fertilization influenced nitrates content in carrots, and the highest NO3concentration was found in carrots fertilized with 120 kg·ha-1of N before sowing. Karotan showed higher nitrates accumulation than Trafford. The content of nitrates in the roots was markedly higher than in carrot juice. Nitrates content in carrots decreased with delaying of harvest time, in opposite to soluble solids content. Soluble solids content and colour parameters of carrot juice were not affected by nitrogen fertilization, but the lowest L*, a*and b*values were observed at the last term of harvest.


2019 ◽  
Vol 245 ◽  
pp. 193-199 ◽  
Author(s):  
Asaad Habibie ◽  
Navid Yazdani ◽  
Mahmoud Koushesh Saba ◽  
Kourosh Vahdati

2000 ◽  
Vol 63 (10) ◽  
pp. 1447-1449 ◽  
Author(s):  
L. STEPANIAK

Different aminopeptidase and endopeptidase substrates were assessed for the detection of enzymatic activity of microorganisms collected from the surface of aerobically cold-stored pork and beef. The most sensitive substrates were fluorogenic Ala-7-amino-4-methylcoumarin (Ala-AMC) or Leu-AMC and colorogenic Ala-p-nitroanilide (Ala-pNA). Activity on natural oligopeptides, e.g., bradykinin or αs1 casein fragment 1 to 23, was very low. The correlation coefficient (r) between log surface counts of 66 meat samples and log fluorescence or absorbance after incubation of surface microbial cells for 2 h with Ala-AMC, Leu-AMC, and Ala-pNA was 0.89, 0.83, and 0.82, respectively. A distinct yellow color was obtained with Ala-pNA when the surface count was ∼106 CFU/cm2. Although correlation and sensitivity was better, no clear advantage is obtained with the use of the fluorogenic Ala-AMC or Leu-AMC instead of Ala-pNA, a substrate proposed by Alvarado et al. (J. Food Sci. 57:1330, 1992) for rapidly assessing the microbial quality of refrigerated meat. The correlation coefficient (r) between time of cold storage and surface count was 0.69.


2019 ◽  
Vol 2 (2) ◽  
pp. 97-101
Author(s):  
Purnama Okviandari

Abstrak Teknik Penyimpanan Krioproservasi  Biakan Agrobacterium tumefaciens : Bahan Penelitian  di  Laboratorium Terpadu dan Sentra Inovasi Teknologi Universitas Jember.  Penelitian merupakan kegiatan yang memerlukan bahan yang berkualitas, salah satu cara menjaga kualitas bahan dengan tehnik penyimpanan yang baik. Pemilihan penggunaan tehnik kriopreservasi pada penelitian ini bertujuan menjaga viabilitas  bakteri dalam jangka waktu tertentu. Teknik kriopreservasi yang digunakan  disesuaikan dengan ketersediaan alat pendingin yang ada. Diharapkan dengan penggunaan tehnik kriopreservasi dapat meningkatkan efiisiensi  dan viabilitas sel dalam jangka waktu enam bulan penyimpanan. Penelitian dilakukan di laboratorium Biologi Molekul dan Bioteknologi  menggunakan Agrobacterium tumefaciens strain GV yang sudah terinsersi gen SPS dalam plasmid pKYS (GVpKYS SPS). Bakteri ditumbuhkan pada media yeast, peptone NaCL dengan penambahan antibiotik 100 ppm rifampisin, 12,5 ppm gentamisin dan 50 ppm kanamisin. Dalam biakan bakteri ditambahkan 15% gliserol sebagai kreoprotektan, kemudian dilakukan pembekuan menggunakan nitrogen cair (-196 °C) dan disimpan selama 6 bulan pada suhu dingin. Analisa yang dilakukan adalah uji viabilitas bakteri dan stabilitas genetik diawal dan akhir masa simpan. Hasil penelitian ini diharapkan dapat menyiapkan bahan penelitian yang berkulaitas dan memberikan informasi teknik penyimpanan dingin yang baik dan effisien pada biakan A. tumefaciens khususnya dan bakteri lain pada umumnya.     Abstrac   Cryoproservation Storage Technique for Agrobacterium tumefaciens Culture : Research Material in Center for Devolepment of Advance Science and Technology (CDAST) University of Jember. This research has tole requires quality materials, one of the way to maintain the quality of materials with good storage techniques. Choosing cryopreservation techniques in this study aims to maintain viability of bacteria in a certain period of time. The cryopreservation technique used is adjusted to the availability of existing cooling devices. It is expected that the use of cryopreservation techniques can improve efficiency and viability of cell within six months of storage. The research was conducted in the Molecular Biology and Biotechnology laboratory using Agrobacterium tumefaciens strain GV which was inserted into the SPS gene in plasmid pKYS (GVpKYS SPS). The bacteria are grown on the yeast, NaCL, peptone media. with the addition of 100 ppm antibiotic rifampicin, 12.5 ppm gentamicin and 50 ppm kanamycin. In culture the bacteria added 15% glycerol for cryoprotectant, then it is freezeed using liquid nitrogen (-196 °C) and stored for 6 months in cold temperatures. The analysis carried out was a viability of bacterial test and genetic stability at the beginning and end of the shelf life. The results of this study are expected to be able to prepare quality research materials and provide information on good and efficient cold storage techniques in particular culture of A. tumefaciens and other bacteria.  


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