Journal of Fermentation Technology最新文献

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Construction of a host-vector system in the osmophilic haploid yeast Zygosaccharomyces rouxii 亲渗单倍体酵母rouxii Zygosaccharomyces宿主载体体系的构建
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90079-9
Kohei Ushio , Hiroki Tatsumi , Hiroyuki Araki , Akio Toh-e , Yasuji Oshima
{"title":"Construction of a host-vector system in the osmophilic haploid yeast Zygosaccharomyces rouxii","authors":"Kohei Ushio ,&nbsp;Hiroki Tatsumi ,&nbsp;Hiroyuki Araki ,&nbsp;Akio Toh-e ,&nbsp;Yasuji Oshima","doi":"10.1016/0385-6380(88)90079-9","DOIUrl":"10.1016/0385-6380(88)90079-9","url":null,"abstract":"<div><p>A host-vector system for <em>Zygosaccharomyces rouxii</em> was developed. Chimeric plasmids useful as the <em>Escherichia coli-Z. rouxii</em> shuttle vector were constructed with a DNA fragment of pBR322, a fragment of pSR1 plasmid of <em>Z. rouxii</em> or the <em>ARS1</em> sequence of <em>Saccharomyces cerevisiae</em>, and a fragment of the <em>LEU2</em> gene of <em>S. cerevisiae</em> or a DNA fragment bearing Tn<em>601</em> which confers G-418 resistance as a selective marker of the plasmid. For the hosts, wild-type strains of <em>Z. rouxii</em> were modified to give improved transformation frequencies or to mark a leucine-auxotrophic mutation which is complementable by the <em>LEU2</em> DNA of <em>S. cerevisiae</em>. Transformation frequencies from several hundred to two thousand transformant clones per μg plasmid DNA samples were obtained.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 5","pages":"Pages 481-488"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90079-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73063183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 24
Promotion factors of flavor production in a liquid fermentation 液体发酵中风味产生的促进因素
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90141-0
Fujio Nakada, Masaaki Hamaji, Takemitsu Honma
{"title":"Promotion factors of flavor production in a liquid fermentation","authors":"Fujio Nakada,&nbsp;Masaaki Hamaji,&nbsp;Takemitsu Honma","doi":"10.1016/0385-6380(88)90141-0","DOIUrl":"10.1016/0385-6380(88)90141-0","url":null,"abstract":"","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 1","pages":"Page 127"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90141-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79539619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Influence of water activity on aroma production by Trichoderma viride TS growing on a solid substrate 水活度对固体基质上生长的绿色木霉产生香气的影响
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90006-4
P. Gervais , J.M. Belin , W. Grajek , M. Sarrette
{"title":"Influence of water activity on aroma production by Trichoderma viride TS growing on a solid substrate","authors":"P. Gervais ,&nbsp;J.M. Belin ,&nbsp;W. Grajek ,&nbsp;M. Sarrette","doi":"10.1016/0385-6380(88)90006-4","DOIUrl":"10.1016/0385-6380(88)90006-4","url":null,"abstract":"<div><p>The influence of water activity on 2-heptanone production (cheese aroma) by <em>Trichoderma viride</em> TS cultivated on agar media was evaluated through a headspace gas chromatographic analysis. Modifications in water activity (<em>a</em><sub>w</sub>) led to a number of variations in the aroma production (300% at 7 d). These variations could be attributed both to an increase in the production rate by the cells and to an increase in mycelial density. Optimal aroma production occurred at <em>a</em><sub>w</sub>=0.98, but considering the radial growth, the optimal <em>a</em><sub>w</sub> values were found to be both 0.96 and 0.98.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 4","pages":"Pages 403-407"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90006-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75523056","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 41
Erythritol production by Aureobasidium sp. SN-115 金黄色葡萄球菌sp. SN-115生产赤藓糖醇
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90020-9
Katsuo Wako , Hiroaki Ishizuka , Gaku Kawaguchi , Naoya Kubo , Takafumi Kasumi , Kiyoshi Hayashi
{"title":"Erythritol production by Aureobasidium sp. SN-115","authors":"Katsuo Wako ,&nbsp;Hiroaki Ishizuka ,&nbsp;Gaku Kawaguchi ,&nbsp;Naoya Kubo ,&nbsp;Takafumi Kasumi ,&nbsp;Kiyoshi Hayashi","doi":"10.1016/0385-6380(88)90020-9","DOIUrl":"10.1016/0385-6380(88)90020-9","url":null,"abstract":"","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 4","pages":"Page 479"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90020-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78611256","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Benzene toxicity and yield improvement in a cis-benzeneglycol production processe 顺式苯乙二醇生产工艺中苯毒性及产率的提高
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90110-0
Jean-Jacques Yarmoff, Yasushi Kawakami, Takeshi Yago, Hajime Nishimura
{"title":"Benzene toxicity and yield improvement in a cis-benzeneglycol production processe","authors":"Jean-Jacques Yarmoff,&nbsp;Yasushi Kawakami,&nbsp;Takeshi Yago,&nbsp;Hajime Nishimura","doi":"10.1016/0385-6380(88)90110-0","DOIUrl":"10.1016/0385-6380(88)90110-0","url":null,"abstract":"<div><p>We carried out experiments designed to increase the production of <em>cis</em>-benzeneglycol from benzene by a mutant strain of <em>Pseudomonas</em>. Factors affecting the production were the temperature, the nitrogen source and it's concentration, the concentration of iron ions, and the benzene concentration. At a benzene concentration of 33% of saturation vapor pressure, the <em>cis</em>-benzeneglycol production was not stable, but this benzene concentration was not toxic to the cells. In a culture under 10% of saturation vapor pressure the cells kept producing <em>cis</em>-benzeneglycol for over 100 h.</p><p>The decrease in <em>cis</em>-benzeneglycol production observed production at high benzen partial pressure (33%) could not be accounted for by the combined effects of an inhibition of enzyme production and a rapid turn-over of the enzyme, but by a specific inactivation of the enzyme. Possible mechanisms of inactivation were discussed which could explain the specific inactivation of the benzene dioxygenase: generation of polyphenols or generation of oxygen radicals.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 3","pages":"Pages 313-321"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90110-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77981865","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Isolation of a fosfomycin-hypersensitive mutant and production of α-d-glucose-l-phosphate from Bacillus sp. BA-3796 screened by its use 芽孢杆菌BA-3796中磷霉素敏感突变体的分离及α-d-葡萄糖-l-磷酸的合成
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90069-6
Takashi Kamogashira, Michiharu Sugawara, Masaaki Takano
{"title":"Isolation of a fosfomycin-hypersensitive mutant and production of α-d-glucose-l-phosphate from Bacillus sp. BA-3796 screened by its use","authors":"Takashi Kamogashira,&nbsp;Michiharu Sugawara,&nbsp;Masaaki Takano","doi":"10.1016/0385-6380(88)90069-6","DOIUrl":"10.1016/0385-6380(88)90069-6","url":null,"abstract":"<div><p>The development of a very sensitive and highly specific screening method for detection of new cell wall inhibitors of the fosfomycin type is described. A fosfomycin-hypersensitive mutant, f-360, was isolated from <em>Staphylococcus aureus</em> Newman by selection with fosfomycin, an antibiotic that inhibits synthesis of the bacterial cell wall. The mutant f-360 was 50-fold more sensitive than the parent strain to fosfomycin. The mutant was constitutive for the hexose phosphate transport system. Using the organism in screening, BA-3796, which had an antibacterial activity against mutant f-360 was found to be produced by a bacterium designated <em>Bacillus</em> sp. BA-3796. Starch and beef extract were the most suitable carbon and nitrogen sources for BA-3796 production and the amount of BA-3796 reached 3 g/<em>l</em> at a maximum level. The purified BA-3796 was identified as α-<span>d</span>-glucose-l-phosphate by its various physiochemical properties. α-<span>d</span>-Glucose-1-phosphate showes an antibacterial activity against <em>Staphylococci</em> in the presence of a slight amount pf α-<span>d</span>-glucose-6-phosphate.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 6","pages":"Pages 649-655"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90069-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76932647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Purification and some properties of β-1,3-glucanase from Trichoderma viride 绿色木霉β-1,3-葡聚糖酶的纯化及其性质研究
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90095-7
{"title":"Purification and some properties of β-1,3-glucanase from Trichoderma viride","authors":"","doi":"10.1016/0385-6380(88)90095-7","DOIUrl":"https://doi.org/10.1016/0385-6380(88)90095-7","url":null,"abstract":"","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 5","pages":"Page 595"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90095-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136914364","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Toxic effects of mercuric ion on the growth of Chlorella sp. in glycine medium 汞离子对甘氨酸培养基中小球藻生长的毒性影响
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90117-3
{"title":"Toxic effects of mercuric ion on the growth of Chlorella sp. in glycine medium","authors":"","doi":"10.1016/0385-6380(88)90117-3","DOIUrl":"https://doi.org/10.1016/0385-6380(88)90117-3","url":null,"abstract":"","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 3","pages":"Page 365"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90117-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137322449","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Microbial Hydroxylation of (−)-α-Santonin by Aspergillus niger 黑曲霉(−)-α-三冬氨酸的微生物羟基化作用
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90129-X
Mitsugi Iida , Akiko Mikami , Koji Yamakawa , Kiyoshi Nishitani
{"title":"Microbial Hydroxylation of (−)-α-Santonin by Aspergillus niger","authors":"Mitsugi Iida ,&nbsp;Akiko Mikami ,&nbsp;Koji Yamakawa ,&nbsp;Kiyoshi Nishitani","doi":"10.1016/0385-6380(88)90129-X","DOIUrl":"10.1016/0385-6380(88)90129-X","url":null,"abstract":"<div><p>The microbiological transformation of a sesquiterpene lactone, (−)-α-santonin was carried out by using <em>Aspergillus niger</em> MIL 5024 and MIL 5025. Strain MIL 5024 brings about the transformation of (−)-α-santonin (400 mg) to 11-hydroxy-(−)-α-santonin (P1) (50.4 mg), 3,6,9-trihydroxy-9,10-<em>seco</em>-selina-1,3,5(10)-trien-12-oic acid-12,6-lactone (P2) (22.4 mg), and 3,6-dihydroxy-9,10-<em>seco</em>-selina-1,3,5(10)-trien-9,12-dioic acid-12,6-lactone (P3) (27.1 mg), which were isolated and characterized by UV, IR, mass and <sup>1</sup>H-NMR spectroanalyses. All of these products are described for the first time. Results similar to those with MIL 5024 were also obtained from the transformation of (−)-α-santonin by the other isolate, strain MIL 5025.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 1","pages":"Pages 51-55"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90129-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89092709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Properties of glucose-dehydrogenase-poly(ethylene glycol)-NAD conjugate as an NADH-regeneration unit in enzyme reactors 葡萄糖-脱氢酶-聚乙二醇-NAD缀合物在酶反应器中作为nadh再生单元的性质
Journal of Fermentation Technology Pub Date : 1988-01-01 DOI: 10.1016/0385-6380(88)90103-3
Akio Nakamura, Hirokazu Minami, Itaru Urabe, Hirosuke Okada
{"title":"Properties of glucose-dehydrogenase-poly(ethylene glycol)-NAD conjugate as an NADH-regeneration unit in enzyme reactors","authors":"Akio Nakamura,&nbsp;Hirokazu Minami,&nbsp;Itaru Urabe,&nbsp;Hirosuke Okada","doi":"10.1016/0385-6380(88)90103-3","DOIUrl":"10.1016/0385-6380(88)90103-3","url":null,"abstract":"<div><p>Glucose-dehydrogenase-poly(ethylene glycol)-NAD conjugate (GlcDH-PEG-NAD) was prepared and its kinetic properties as an NADH-regeneration unit were investigated. The conjugate has about two molecules of active and covalently linked NAD per tetramer. The specific activity of the enzyme moiety of the conjugate in the presence of exogenous NAD is about 77% of that of the native enzyme, and this decrease is mainly due to the decrease in the <em>V</em><sub>max</sub> value. The conjugate has the same pH-stability profile as the native enzyme and an internal activity of 0.26s<sup>−1</sup> (as a monomer); its NAD moiety has similar coenzyme activity to poly(ethylene glycol)-bound NAD. These results indicate that GlcDH-PEG-NAD can be used as an NADH-regeneration unit for many dehydrogenase reactions. The coupled reaction of GlcDH-PEG-NAD and lactate dehydrogenase was then studied. The specific activity of the conjugate is 1.1 s<sup>−1</sup> (as a tetramer), the recycling rate of the active NAD moiety is 0.54 s<sup>−1</sup>, and the apparent <em>K</em><sub>m</sub> value for glucose is 24 mM. Kinetically, lactate dehydrogenase behaves like a substrate with an apparent <em>K</em><sub>m</sub> value of 1.8 units·ml<sup>−1</sup> in this coupled reaction system with low coenzyme concentration. <span>l</span>-Lactate was continuously produced from pyruvate in a reactor with a PM10 ultrafiltration membrane, and containing GlcDH-PEG-NAD and lactate dehydrogenase. GlcDH-PEG-NAD proved to be applicable in continuous enzyme reactors as an NADH-regeneration unit with a large molecular size.</p></div>","PeriodicalId":15702,"journal":{"name":"Journal of Fermentation Technology","volume":"66 3","pages":"Pages 267-272"},"PeriodicalIF":0.0,"publicationDate":"1988-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0385-6380(88)90103-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89333861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
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