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1.
S. Genovés J.V. Gil P. Manzanares J.L. Aleixandre S. Vallés 《Journal of food science》2003,68(6):2096-2100
ABSTRACT: A recombinant Saccharomyces cerevisiae wine yeast strain expressing the Candida molischiana bgln gene encoding a β-glucosidase (BGLN) has been used to produce this enzyme. Shaking rate, pH, and aeration rate conditions have been optimized to obtain maximum activity to facilitate enzyme purification. The ability of the heterologous enzyme to efficiently release terpenols and alcohols from a Muscat wine glycoside extract and also directly from wine has been demonstrated. Terpenol glycoside content decreased by 50% after 1 mo of wine storage in agreement with results reported for the β-glucosidase produced by C. molischiana. 相似文献
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Yukihisa Tanaka Jiro Hirano Tadashi Funada 《Journal of the American Oil Chemists' Society》1992,69(12):1210-1214
In an attempt to concentrate the content of DHA (docosahexaenoic acid) in a glyceride mixture containing triglyceride, diglyceride
and monoglyceride, fish oil was hydrolyzed with six kinds of microbial lipase. After the hydrolysis, free fatty acid was removed
and fatty acid components of the glyceride mixtures were analyzed. When the hydrolysis withCandida cylindracea lipase was 70% complete, the DHA content in the glyceride mixture was three times more than that in the original fish oil.
The EPA (eicosapentaenoic acid) content became almost 70% of the original fish oil. Hydrolysis with other lipases did not
result in an increase in the DHA content in the glyceride mixtures. Hydrolysis of DHA-rich tuna oil (DHA content is about
25%) withCandida cylindracea lipase resulted in 53% DHA in the glyceride mixture. The EPA content, however, remained close to that of the original tuna
oil. In this report, the acyl chain specificity of lipases is evaluated in terms of hydrolysis resistant value (HRV). HRV
is the ratio between the DHA contents in the glyceride mixture of hydrolyzed oil and original oil. HRV clearly indicates differences
in hydrolysis between DHA and other fatty acids (e.g., saturated and monoenoic acids). 相似文献
4.
Assignment of most genes encoding major peroxisomal polypeptides to chromosomal band V of the asporogenic yeast Candida tropicalis 总被引:1,自引:0,他引:1
The peroxisomes of the asporogenic yeast Candida tropicalis contain about 20 major polypeptides (PXPs). We have isolated a number of genes encoding them; 11 POX genes encoded independent PXPs and three POY genes were likely to encode three other PXPs. To locate these genes on the chromosomes, chromosomes of C. tropicalis were separated by pulsed-field gel electrophoresis. Eight chromosomal bands were observed over the range of 1.0 Mbp (band 1) to 2.8 Mbp (band VIII); the genome size was estimated to be about 20 Mbp. Southern blot analysis showed that ten genes were on band V, three genes were on band IV, and the other gene was on band VI. Three genes gave hybridization signals of nearly equal intensity on two different chromosomal bands: POX6A and POX8B, on bands V and VII; and POX8A, on bands IV and VI. Ribosomal RNA genes also hybridized to two bands, VI and VII. Most genes assigned to only one band hybridized to two restriction fragments produced by either NotI or SfiI endonuclease. The results suggested that C. tropicalis was diploid and that restriction sites were conserved little between homologues. The three POX genes that were found on two chromosomal bands hybridized to not more than two restriction fragments, implying that the allelic genes were present on different chromosomal bands. 相似文献
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Carmen de Jesús-Gil Lídia Sans-de San Nicols Ester Ruiz-Romeu Marta Ferran Laura Soria-Martínez Irene García-Jimnez Anca Chiriac Josep Manel Casanova-Seuma Josep Manel Fernndez-Armenteros Sherry Owens Antonio Celada Michael D. Howell Ramn María Pujol Luis Francisco Santamaria-Babí 《International journal of molecular sciences》2021,22(4)
Candida albicans (CA) infections have been associated with psoriasis onset or disease flares. However, the integrated immune response against this fungus is still poorly characterized in psoriasis. We studied specific immunoglobulins in plasma and the CA response in cocultures of circulating memory CD45RA− cutaneous lymphocyte antigen (CLA)+/− T cell with autologous epidermal cells from plaque and guttate psoriasis patients (cohort 1, n = 52), and also healthy individuals (n = 17). A complete proteomic profile was also evaluated in plaque psoriasis patients (cohort 2, n = 114) regarding their anti-CA IgA levels. Increased anti-CA IgA and IgG levels are present in the plasma from plaque but not guttate psoriasis compared to healthy controls. CA cellular response is confined to CLA+ T cells and is primarily Th17. The levels of anti-CA IgA are directly associated with CLA+ Th17 response in plaque psoriasis. Proteomic analysis revealed distinct profiles in psoriasis patients with high anti-CA IgA. C-C motif chemokine ligand 18, chitinase-3-like protein 1 and azurocidin were significantly elevated in the plasma from plaque psoriasis patients with high anti-CA levels and severe disease. Our results indicate a mechanism by which Candida albicans exposure can trigger a clinically relevant IL-17 response in psoriasis. Assessing anti-CA IgA levels may be useful in order to evaluate chronic psoriasis patients. 相似文献
8.
响应面优化褶皱假丝酵母脂肪酶催化合成木质甾醇油酸酯 总被引:1,自引:0,他引:1
以木质甾醇转化率为指标,考察了10种常见商业化脂肪酶催化合成木质甾醇油酸酯的效果,确定褶皱假丝酵母脂肪酶(CRL)为优选生物催化剂,进一步筛选出正己烷为优选反应介质.在脂肪酶用量、油酸和木质甾醇的物质的量比、反应温度和反应时间这4个单因素考察基础上,通过响应面分析法对酶催化木质甾醇油酸酯合成工艺条件进行优化,并对优化条件进行验证和放大实验.CRL催化合成木质甾醇油酸酯的优化工艺参数为:CRL添加量为木质甾醇质量的10%,油酸与木质甾醇的物质的量比为3.8:1,反应温度为46℃,反应时间为28 h,木质甾醇的转化率为91.56%±0.25%. 相似文献
9.
南极假丝酵母脂肪酶发酵条件优化及酶学性质 总被引:7,自引:0,他引:7
分别用摇瓶和15L发酵罐,对南极假丝酵母产胞外脂肪酶的培养基成分和操作条件进行了实验研究。得到最优的培养基组成为:豆粉40g/L,淀粉15g/L,豆油5mL/L,K2HPO4g/L,MgsO4·7H2O1g/L,Tween-800.1%,酵母膏5g/L;操作条件为:温度24℃,初始pH值为6.0,通气量为10.0L/min。在此培养条件下,发酵周期缩短至54h。由15L发酵罐生产的酶液酶活达到19.2U/mL。酶液在pH值为4.0~6.0和7.5~9.0范围内较稳定,其最适宜pH值范围为6~8.5;70℃时酶的催化活性最大.在40~70℃的温度范围内保持1h后残留酶活为60%。 相似文献
10.
Taeko Izumi Yoshihiro Yagimuma Masanori Haga 《Journal of the American Oil Chemists' Society》1997,74(7):875-878
Enyzmatic amidation of the primary amines β-alanine ethyl ester and 3-aminopropionitrile with methyl laurate by means of immobilized
lipase (Candida antarctica lipase, CAL) resulted in the formation in good yield of N-lauroyl-β-alanine ethyl ester and 3-(N-lauroylamino)-propionitrile, respectively. When 3-amino-propionitrile was used as substrate, diisopropyl ether was a suitable
solvent. Changing the reaction temperature (12–80°C) did not affect the yields, and room temperature was a suitable temperature
for this reaction. In the investigation of reaction conditions, the use of equimolar amounts (5 mmol) of substrate and ester,
along with 0.5 g of CAL, in diisopropyl ether gave the best yield (99.3%) after 24 h of incubation at 24°C. The enzyme activity
in the amidation reaction did not decrease even after six uses. With β-alanine ethyl ester hydrochloride as substrate, diisopropyl
ether was unsuited as a solvent owing to the low solubility of the substrate in this solvent.
In this reaction, the best yield (82.0%) was attained by using dioxane as solvent. CAL achieved higher extents of amide synthesis
with long-chain than with short-chain ester substrates. The enzyme accepted only nonbulky primary amines as substrates. 相似文献