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Mortierella ramanniana

Bile acids have historically received much less attention than other steroids, for example the corticosteroids however, now that useful thertqreutic effects ate being observed from some bile acids, there is fresh interest in Ais area. A strain of Cunninghamella Uakesleeana has been isolated that will 15p-hy-droxylate lithocholic acid (80 equation 26) in 31% yield.Further reaction is possible to give 3a,lip,15p-trihydroxy-5p-cholanic acid (15%), 3a,15p,18a-trihydioxy-5p-cholanic acid (4%) and 3a,lla,15p-trihydroxycholanic acid (9%). Taurolithocholic acid (81 equation 27) can be 7p-hydroxy-lated in virtually quantitative yield by Mortierella ramanniana. ... [Pg.73]

Extracted from fungi Mortierella ramanniana var. angulispora). [Pg.380]

Lardizabal, K.D., J.T. Mai, N.W. Wagner, A. Wyrick, T. Voelker, and D.J. Hawkins. 2001. DGAT2 is a new diacylglycerol acyltransferase gene family purification, cloning, and expression in insect cells of two polypeptides from Mortierella ramanniana with diacylglycerol acyltransferase activity. J. Biol Chem. 276 38862-38869. [Pg.17]

Anderson HA, Thomson RH, Wells JW (1966) Naturally occurring quinones. Part VIII. Solorinic acid and norsolorinic acid. J Chem Soc (C) 1727-1729 Andres WW, Kunstmann MP, Mitscher LA (1967) Isolation and structure of 2,4-dihydroxy-3,5,6-trimethylbenzoic acid from Mortierella ramanniana. Experientia 23 703-704... [Pg.447]

TABLE 2. Lipid profiles of subcellular fractions of Mortierella ramanniana var. angulispora. Data are presented as means of triplicates S.D. [Pg.539]

Mortierella ramanniana Commercial-scale batch bioreactor Glucose 62 46.1 N.A. Hiruta et al. (1996)... [Pg.206]

Hiruta, O., Futamura, T., Takebe, H., Satoh, A., Kantisaka, Y., Yokochi, T., Nakahara, T., Suzuki, O., 1996. Optimization and scale-up of gamma-linolenic acid production by Mortierella ramanniana MM 15-1, a high gamma-finolenic acid producing mutant. Journal of Fermentation and Bioengineering 82, 366—370. [Pg.229]

Figure 24 Oxygenation of 2,2-dimethyl-2H-l-benzopyran-6-carbonitrile 74 to the corresponding chiral epoxide 72 and (+)-rmni -diol 73 by Mortierella ramanniana SC 13840. Figure 24 Oxygenation of 2,2-dimethyl-2H-l-benzopyran-6-carbonitrile 74 to the corresponding chiral epoxide 72 and (+)-rmni -diol 73 by Mortierella ramanniana SC 13840.
Dimethyl 2H-benzopyran-6-carbonitrile -3S,4S-epoxide Corynebacterium sp. Mortierella ramanniana 85... [Pg.196]

See other pages where Mortierella ramanniana is mentioned: [Pg.369]    [Pg.163]    [Pg.1493]    [Pg.39]    [Pg.157]    [Pg.105]    [Pg.990]    [Pg.105]    [Pg.108]    [Pg.372]    [Pg.532]   
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