Investigating the Production of Secondary Compounds in Cultured Lichen Mycobionts

2002 ◽  
pp. 296-306 ◽  
Author(s):  
Elfie Stocker-Wörgötter
Keyword(s):  
Secondary Compounds

Mycobiont and Whole Thallus Cultures of Roccella Montagnei Bél. For the Biosynthesis of Secondary Compounds

2016 ◽  
Vol 1 (1) ◽  
Author(s):  
G.N. Hariharan ◽  
S. Karthik ◽  
S. Muthukumar
Keyword(s):  
Carbon Source ◽  
Incubation Period ◽  
Internal Transcribed Spacer ◽  
Secondary Compounds ◽  
Acetone Extract ◽  
Optimum Growth ◽  
Secondary Chemistry ◽  
Molecular Identity ◽  
Secondary Compound

The mycobiont and whole thallus cultures of Roccella montagnei Bel. were established using soredia as an inoculum.The mycobiont cultures showed optimum growth, biomass and biosynthesis of compounds in Lilly and Barnett medium with glucose as a carbon source, micronutrients and vitamins. After the incubation period of 180 days, the cultures were harvested, and their biomass and secondary compound profiles were analysed. The HPTLC chromatogram of the acetone extract of the NT and mycobiont cultures revealed erythrinas the major biosynthesized compound in both and identified as a key biosynthate by R. montagnei. Further, the NT biosynthesized 5 additional compounds and themycobiont cultures biosynthesized 6 additional compounds. The molecular identity of the cultured mycobiont was confirmed using nuclear ribosomal Internal Transcribed Spacer (ITS) as well as the secondary chemistry. Lichen compound erythrin was identified as a key biosynthate by the cultures.

scholarly journals β-Ketophosphonates with Pentalenofuran Scaffolds Linked to the Ketone Group for the Synthesis of Prostaglandin Analogs

2021 ◽  
Vol 22 (13) ◽  
pp. 6787
Author(s):  
Constantin I. Tănase ◽  
Constantin Drăghici ◽  
Miron Teodor Căproiu ◽  
Anamaria Hanganu ◽  
Gheorghe Borodi ◽  
...  
Keyword(s):  
Lithium Salt ◽  
Methyl Esters ◽  
Secondary Compounds ◽  
Molecular Structures ◽  
Keto Group ◽  
High Yield ◽  
Oxidation Reactions ◽  
Prostaglandin Analogues ◽  
X Ray ◽  
Oxidation Of Alcohols

β-Ketophosphonates with pentalenofurane fragments linked to the keto group were synthesized. The bulky pentalenofurane skeleton is expected to introduce more hindrance in the prostaglandin analogues of type III, greater than that obtained with the bicyclo[3.3.0]oct(a)ene fragments of prostaglandin analogues I and II, to slow down (retard) the inactivation of the prostaglandin analogues by oxidation of 15α-OH to the 15-keto group via the 15-PGDH pathway. Their synthesis was performed by a sequence of three high yield reactions, starting from the pentalenofurane alcohols 2, oxidation of alcohols to acids 3, esterification of acids 3 to methyl esters 4 and reaction of the esters 4 with lithium salt of dimethyl methanephosphonate at low temperature. The secondary compounds 6b and 6c were formed in small amounts in the oxidation reactions of 2b and 2c, and the NMR spectroscopy showed that their structure is that of an ester of the acid with the starting alcohol. Their molecular structures were confirmed by single crystal X-ray determination method for 6c and XRPD powder method for 6b.

scholarly journals Fungal-Fungal Interactions in Leaf-Cutting Ant Agriculture

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Sunshine A. Van Bael ◽  
Catalina Estrada ◽  
William T. Wcislo
Keyword(s):  
Plant Traits ◽  
Secondary Compounds ◽  
Future Research ◽  
Ecological Interactions ◽  
Tropical Plants ◽  
Symbiotic Relationships ◽  
Complex Interactions ◽  
Symbiotic Fungi ◽  
Leaf Cutting ◽  
Fungal Interactions

Many organisms participate in symbiotic relationships with other organisms, yet studies of symbioses typically have focused on the reciprocal costs and benefits within a particular host-symbiont pair. Recent studies indicate that many ecological interactions involve alliances of symbionts acting together as mutualistic consortia against other consortia. Such interacting consortia are likely to be widespread in nature, even if the interactions often occur in a cryptic fashion. Little theory and empirical data exist concerning how these complex interactions shape ecological outcomes in nature. Here, we review recent work on fungal-fungal interactions between two consortia: (i) leaf-cutting ants and their symbiotic fungi (the latter grown as a food crop by the former) and (ii) tropical plants and their foliar endophytes (the cryptic symbiotic fungi within leaves of the former). Plant characteristics (e.g., secondary compounds or leaf physical properties of leaves) are involved in leaf-cutting ant preferences, and a synthesis of published information suggests that these plant traits could be modified by fungal presence. We discuss potential mechanisms for how fungal-fungal interactions proceed in the leaf-cutting ant agriculture and suggest themes for future research.

Physiological Effect of Lichen Secondary Metabolites on the Lichen Parasite Marchandiomyces Corallinus

1999 ◽  
Vol 31 (3) ◽  
pp. 307-314 ◽  
Author(s):  
A. P. Torzilli ◽  
P. A. Mikelson ◽  
J. D. Lawrey
Keyword(s):  
Catalytic Activity ◽  
Phenolic Compounds ◽  
Secondary Metabolites ◽  
Host Preference ◽  
Secondary Compounds ◽  
Physiological Effect ◽  
Physiological Adaptation ◽  
Secondary Chemistry ◽  
Physiological Basis ◽  
Lichenicolous Fungi

AbstractIt has been suggested that the host specificity exhibited by some lichenicolous fungi depends on their ability to tolerate the secondary chemistry of potential host lichens. For example, the lichen parasite Marchandiomyces corallinus is able to degrade the tissues of the lichen Flavoparmelia baltimorensis irrespective of the presence or absence of endogenous phenolic compounds. In contrast, the degradation of tissues from the lichen Lasallia papulosa is suppressed when endogenous phenolics are not removed. We have investigated the physiological basis of this inhibition in order to understand more about how lichen chemistry infiuences host preference in lichenicolous fungi. Results showed that the secondary compounds from L. papulosa inhibit the overall growth of M. corallimis, but not the catalytic activity of its tissue-degrading polysaccharidases. This effect is different from that shown by another lichen parasite, Nectria parmeliae, where lichen compounds specifically inhibited polysaccharidase activity. Compared with the compounds of L. papulosa, the endogenous phenolics of F. baltimorensis inhibited the growth of M. corallimis substantially less and exhibited little or no inhibition of polysaccharidases. For M. corallimis, host preference appears to be associated with physiological adaptation to the chemistry of F. baltimorensis.

Effects of age and food source on secondary chemistry of larvae of Lymantria species (Lepidoptera: Lymantriidae)

2004 ◽  
Vol 94 (2) ◽  
pp. 137-143 ◽  
Author(s):  
R. Deml
Keyword(s):  
Secondary Metabolites ◽  
Developmental Stages ◽  
Secondary Compounds ◽  
Food Plants ◽  
Gas Chromatography Mass Spectrometry ◽  
Chemical Compositions ◽  
Clustering Methods ◽  
Single Linkage ◽  
Secondary Chemistry ◽  
Dissimilarity Coefficients

AbstractHaemolymph and osmeterial secretions of caterpillars of Lymantria monacha (Linnaeus) and L. concolor Walker were analysed by gas chromatography/mass spectrometry for low molecular weight secondary metabolites. The similarities of their chemical compositions were determined by means of cluster analysis techniques in order to characterize possible chemical variations related to developmental stage or food of the larvae. For this purpose, two dissimilarity coefficients (Euclidean distances, Canberra metrics) and four clustering methods (UPGMA, WPGMA, WPGMC, single linkage) were combined. The patterns of secondary compounds obtained from the haemolymph and osmeterial secretions studied did not differ statistically significantly between two groups of L. monacha larvae fed with either larch, Larix decidua Mil., or Norway spruce, Picea abies (L.), indicating no relevant influence of plant chemistry. However, haemolymph of penultimate instar larvae of L. concolor fed on Rhododendroncontained a mixture of compounds differing statistically significantly from that of last instar caterpillars. The total compositions of the corresponding gland secretions were statistically identical though the presence/amounts of individual compounds varied. This suggested that the haemolymph composition reflected changing physiological requirements of the successive instars, whereas the composition of the defensive mixtures remained comparatively constant, possibly due to a constant spectrum of potential enemies. A more pronounced age-dependence of larval chemistry was shown by a similar analysis of data from various developmental stages of L. dispar (Linnaeus) and one of its food plants. This analysis suggested plant composition affected the secondary chemistry of early larval instars of L. dispar. The results are discussed in terms of the roles of secondary metabolites in defence against natural enemies.

scholarly journals Effects of Increasing Doses of Condensed Tannins Extract from Cistus ladanifer L. on In Vitro Ruminal Fermentation and Biohydrogenation

Animals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 761
Author(s):  
Olinda Guerreiro ◽  
Susana P. Alves ◽  
Mónica Costa ◽  
Maria F. Duarte ◽  
Eliana Jerónimo ◽  
...  
Keyword(s):  
Fatty Acids ◽  
Condensed Tannins ◽  
Volatile Fatty Acids ◽  
Secondary Compounds ◽  
Cistus Ladanifer ◽  
Ruminal Fermentation ◽  
Experimental Conditions ◽  
Ct Dose ◽  
Linear Decrease

Cistus ladanifer (rockrose) is a perennial shrub quite abundant in the Mediterranean region, and it is a rich source in secondary compounds such as condensed tannins (CTs). Condensed tannins from C. ladanifer were able to change the ruminal biohydrogenation (BH), increasing the t11–18:1 and c9,t11–18:2 production. However, the adequate conditions of the C. ladanifer CTs used to optimize the production of t11–18:1 and c9,t11–18:2 is not yet known. Thus, we tested the effect of increasing the doses of C. ladanifer CT extract (0, 25, 50, 75 and 100 g/kg dry matter (DM)) on in vitro rumen BH. Five in vitro batch incubations replicates were conducted using an oil supplemented high-concentrate substrate, incubated for 24 h with 6 mL of buffered ruminal fluid. Volatile fatty acids (VFAs) and long chain fatty acids (FA) were analyzed at 0 h and 24 h, and BH of c9–18:1, c9, c12–18:2 and c9, c12, c15–18:3, and BH products yield were computed. Increasing doses of C. ladanifer CTs led to a moderate linear decrease (p < 0.001) of the VFA production (a reduction of 27% with the highest dose compared to control). The disappearance of c9–18:1 and c9,c12–18:2 as well as the production of t11–18:1 and c9, t11:18:2 was not affected by increasing doses of C. ladanifer CTs, and only the disappearance of c9, c12, c15–18:3 suffered a mild linear decrease (a reduction of 24% with the highest dose compared to control). Nevertheless, increasing the C. ladanifer CT dose led to a strong depression of microbial odd and branched fatty acids and of dimethyl acetals production (less than 65% with the highest dose compared to control), which indicates that microbial growth was more inhibited than fermentative and biohydrogenation activities, in a possible adaptative response of microbial population to stress induced to CTs and polyunsaturated fatty acids. The ability of C. ladanifer to modulate the ruminal BH was not verified in the current in vitro experimental conditions, emphasizing the inconsistent BH response to CTs and highlighting the need to continue seeking the optimal conditions for using CTs to improve the fatty acid profile of ruminant fat.

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