ChemInform Abstract: In vitro Prenylation of Aromatic Intermediates in the Biosynthesis of Bitter Acids in Humulus lupulus.

ChemInform ◽  
2010 ◽  
Vol 30 (20) ◽  
pp. no-no
Author(s):  
Karin W. M. Zuurbier ◽  
Suen-Ying Fung ◽  
Johannes J. C. Scheffer ◽  
Robert Verpoorte
Keyword(s):  
1998 ◽  
Vol 49 (8) ◽  
pp. 2315-2322 ◽  
Author(s):  
Karin W.M. Zuurbier ◽  
Suen-Ying Fung ◽  
Johannes J.C. Scheffer ◽  
Robert Verpoorte
Keyword(s):  

2013 ◽  
Vol 12 (2) ◽  
pp. 129-140
Author(s):  
Maria Maliarova ◽  
Tibor Maliar ◽  
Jana Girmanova ◽  
Jozef Lehotay ◽  
Jan Kraic

Abstract The Humulus lupulus L. is well known as necessary raw material for beer production. The main structural classes of chemical compounds identified from hop cones include terpenes, bitter acids, prenylated chalcones, and flavonol glycosides. They were subjects of presented work. The content of quercetin was found in the range 490 - 1092 μg/g and that of kaempferol from 218 to 568 μg/g of the dry hop cones. The content of isorhamnetin was very low in all varieties. From biological activities in vitro point of view, relative high level of inhibition activity was observed for six hop genotypes - Zlatan, Lučan, and the Oswald's clones 31, 70, 71, 72, 114 on both enzymes thrombin and urokinase, but without correlation to analyzed flavonols content. In spite of this, antioxidant activity, measured by both the BCLM and HPE methods, was found high and seem to be in correlation with content of analyzed flavonols. Particularly the Oswald's clone 114 expressed very potent biological activities. In general, obtained results indicate that hop cones are valuable material also for other application others than beer production.


2013 ◽  
Vol 57 (6) ◽  
pp. 1055-1066 ◽  
Author(s):  
Birgit M. Dietz ◽  
Ghenet K. Hagos ◽  
Jillian N. Eskra ◽  
Gihani T. Wijewickrama ◽  
Jeffrey R. Anderson ◽  
...  

2016 ◽  
Vol 28 (1) ◽  
pp. 50-57 ◽  
Author(s):  
Daniel P. Killeen ◽  
Oliver C. Watkins ◽  
Catherine E. Sansom ◽  
David H. Andersen ◽  
Keith C. Gordon ◽  
...  

2019 ◽  
Vol 72 (2) ◽  
Author(s):  
Michaela Švécarová ◽  
Božena Navrátilová ◽  
Petr Hašler ◽  
Vladan Ondřej

The aim of the research was to establish an efficient procedure for in vitro micropropagation in order to obtain numbers of identical plants for in vitro polyploidization of <em>Humulus lupulus</em> (2<em>n</em> = 20), using antimicrotubule agent oryzalin. For this purpose, the polyploidization was carried out for <em>H. lupulus</em> Osvald’s clones 31, 74, 114, and for ‘Sladek’ cultivar. The two experimental methods – the cultivation of nodal segments on medium with different concentrations of oryzalin (1, 5, and 10 µM) for 2 weeks and the irrigation of nodal segments with oryzalin (10 and 20 µM) for 24 and 48 h were chosen for inducing for polyploid plantlets of <em>H. lupulus</em>. This procedure provided tetraploids, which were identified by flow cytometry using internal standardization method and confirmed using chromosome counting of methaphasic cells from the root tips and morphological observations. The influence of chromosome doubling was also verified with stomata characterization. The polyploid plants were propagated for next evaluation, rooting and transfer to nonsterile conditions and into field. After chromosome doubling, using some different concentration of oryzalin, some plantlets became tetraploids, no mixoploids were detected. The highest efficiency of polyploidization was achieved for clone 72 after 2-week treatment of oryzalin supplemented medium. On the other hand, for method based on the irrigation of nodal segments with oryzalin, the most efficient conditions were treatment with 10 µM and 20 µM oryzalin for 24 and 48 h, respectively.


2011 ◽  
Vol 49 (01) ◽  
Author(s):  
M Saugspier ◽  
C Dorn ◽  
M Gehrig ◽  
J Heilmann ◽  
C Hellerbrand

2020 ◽  
Vol 56 (No. 4) ◽  
pp. 159-164
Author(s):  
Josef Patzak ◽  
Alena Henychová ◽  
Petr Svoboda ◽  
Ivana Malířová

In vitro meristem cultures have been used for the production of hop (Humulus lupulus L.) virus-free rootstocks worldwide, because multipropagation is considered to preserve the genetic stability of the produced plantlet. Nevertheless, in vitro tissue cultures can cause genetic and epigenetic changes. Therefore, we studied the genetic and epigenetic variability of Saaz Osvald’s clones, Sládek and Premiant cultivars on the DNA methylation level by methylation-sensitive amplification polymorphism (MSAP). In vitro propagated plants, acclimatised glasshouse rootstocks as well as derived mericlones and control plants under field conditions were used for the analyses. A total of 346 clearly and highly reproducible amplified products were detected in the MSAP analyses within the studied hop plants. We found 16 polymorphic products (4.6% of products) and 64 products with methylation changes (18.5% of products) in the analyses. The demethylation events were comparable to the de novo methylation events. Most demethylation changes were found in the in vitro plants, but only a few of them were found in the derived mericlones under field conditions. In contrast, the de novo methylation changes persisted in the acclimatised plants under glasshouse or field conditions. A hierarchical cluster analysis was used for the evaluation of the molecular genetic variability within the individual samples. The dendrogram showed that the individual samples of the same variety, more or less, clustered together. Because the methylation status varied during the virus-free rootstock production process, we suppose that de/methylation process is a natural tool of epigenetics and evolution in vegetatively propagated plants.


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