Absidia glauca

Absidia glauca, Cunninghamella blakesleeana, Cunninghamella sp., Fusarium solan f. sp. cucurbitae, and Rhizopogon sp. 

For the screening, 25 microbial cultures, obtained from the University of Mississippi Department of Pharmacognosy culture collection, were used. Microbial bioconversion studies of sarcophine (45) showed that it can be metabolized by several fungi species. Preparative-scale fermentation with Absidia glauca American-type culture collection (ATCC) 22752, Rhizopus arrhizus ATCC 11145, and R. stolonifer ATCC 24795 resulted in the isolation... 

In auxotrophic mutants of Absidia glauca, a specific gene transfer from the parasite Parasitella parasitica to the host A. glauca was detected by Kellner et al. [108] and Wostemeyer et al. [109]. 

Ophiostoma (versch. Arten). . Absidia glauca, Aspergillus niger und viele andere + +... 

Biological oxidation of the hydrocarbon adamantane by the fungus Absidia glauca gives a mixture of two alcohols. Classify the carbon in adamantane that is oxidized in forming the major product. 

Linalyl acetate (206-Ac) was hydrolyzed to (-t)-(5)-linalool (206) and (i)-linalyl acetate (206-Ac) by Bacillus subtilis, Trichoderma S, Absidia glauca, and Gibberella fujikuroi as shown... 

FIGURE 19.106 Metabolic pathways of (-)-carvone (93 ) by Aspergillus niger TBUYN-2 and Absidia glauca ATCC 22752. (Modi ed from Demirci, F. et al.. The biotransformation of thymol methyl ether by dif ferent fungi. Book of Abstracts of the XII Biotechnology Congr., p. 47, 2001.)... 

On the other hand, Absidia glauca converted (-)-carvone (93 ) stereospecificaUy to give (+)-8-p-menthene-2,8-diol (107a ) via (+)-dihydrocarvone (101a ) and (-i-)-neodihydrocarveol (102a ) (Demirci et al., 2004) (Figure 14.93). 

In case of the plant pathogenic fungus Absidia glauca (-)-carvone (93 ) was metabolized to give the diol, 10-hydroxy-(+)-neodihydrocarveol (107a ) (Nishimuia et al., 1983b). 

The fxmgus Absidia glauca [55], used as suspended cells in buffer, transformed 3-oxo-olean-12-en-28-oic acid (52) into three metabolites ip,lla-dihydroxy-3-oxo-olean-12-en-28-oic acid (64), lp,lla,2ip-trihydroxy-3-oxo-olean-12-en-28-oic acid (66), and ip-hydroxy-3-oxo-olean-ll-en-28(13)-olide (65) (Figure 28.15). 

Microbial transformation of 3-oxo-olean-12-en-28-oic (52) acid by Absidia glauca [56] and Chaetomium longirostre [57],... 

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