• Title/Summary/Keyword: Hansenula anomala

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Isolation and Identification of the Amylolytic Yeast Hansenula and its Haploid Mutant (전분이용성 Hansenula의 분리동정 및 변리주 개발)

  • 구영조;박완수;신동화;유태종
    • Microbiology and Biotechnology Letters
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    • v.13 no.2
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    • pp.129-135
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    • 1985
  • The amylolytic yeasts were isolated from natural sources. Among them, a strain FRI YO-32 was selected as one of the genetically potential microorganisms and was identified as a strain of Hansenula anomala var anomala. Genetic markers were introduced into the isolated haploid strains of the strain FRI YO-32 and Saccharomyces cerevisiae by conventional mutagenic procedures with EMS or MNNG.

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Preventive Effect of Lysis in the Cadmium-Tolerant Hansenula anomala B-7 Cells by Metal Ions (금속 이온에 의한 카드늄 내성균주 Hansenula anomala B-7 세포의 용균 방지 효과)

  • Song, Hyung-Ik;Yu, Tae-Shick
    • The Korean Journal of Mycology
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    • v.19 no.4
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    • pp.282-284
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    • 1991
  • The yeast, Hansenula anomala B-7, isolated from the $Cd^{2+}$ rich soils and determined to be tolerant in the high concentration of $Cd^{2+}$ were employed in this work. Its intact cells grown in high concentration of $Cd^{2+}$ were observed to be Iysed at the early stage when transferred to a cadmium deficient broth. Its intact cells found to be not Iysed and grow well under the high concentration of $Cd^{2+}$. The Iysis of the intact cells grown at the high concentration of $Cd^{2+}$ ion was not found when the metal ions were replaced with $Cd^{2+}$ ion in the same concentration. This result indicated that Iysis of yeast cells, at least in this isolate, would be related to cell osmosis with the mineral ions added.

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Effect of Triton X-100 on Intracellular Accumulation of Cadmium in Hansenula anomala (카드뮴의 Hansenula anomala 세포내 축적에 미치는 Triton X-100의 효과)

  • 유대식;박정문;송형익
    • Korean Journal of Microbiology
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    • v.25 no.2
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    • pp.110-116
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    • 1987
  • As a pary of investgation on effective accumulation of cadmium in yeast cells, effect of surfactant was studied on intracellular accumulation of cadmium in extremely cadmium-tolerant yeast, Hansenula anomala B-7. Cadmium accumulation was enhanced up to approximately 40% by the addition of non-ionic surfactant, Triton X-100 and its optimal concentration was found to be 0.1-0.2%. Furthermore, optimum conditions for intracellular accumulation of cadmium were at $40^{\circ}C$ and initial pH 6.0 for 48 hours under shaking culture.

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Morphological Changes of Hansenula anomala B-7 by Cadmium Ion (카드뮴이온에 의한 Hansenula anomala B-7의 형태 변이)

  • 송형익;유대식
    • Korean Journal of Microbiology
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    • v.29 no.6
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    • pp.397-401
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    • 1991
  • Yeast-form cells of cadmium ion-tolerant Hansenula anomala B-7 were changed to mycelial cells in medium containing more than $400\mu$g/ml of cadmium. Moreover, the mycelial cells were exchanged into clumped cells in a medium containing more than $1,000\mu$g/ml of cadmium. Optimal conditions of mycelial cell formation were achieved in the presence of .$1,000\mu$g/ml of cadmium with shaking cultivation for 7 days. Glucan and mannan contents of the yeast cell wall frown with $1,000\mu$g/ml of cadmium decreased by 10% compared with those grown without cadmium. However, protein and lipid contents increased about 20% respectively. By cadmium, no significant findings in specific amino acid contents were discovered.

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Characterzation of a Cadmium-ion Tolerant Strain of Hansenula anomala (카드뮴 내성 Hansenula anomala 균주의 특성)

  • 유대식;송형익;정기택
    • Korean Journal of Microbiology
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    • v.24 no.1
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    • pp.57-61
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    • 1986
  • In order to remove of cadmium from waste water an identification of a cadmium-ion tolerant yeast B-7 isolated from the sludge of zinc mining district was studied. By the taxonomecal characteristics of strain B-7 it was identified as Hansenula anomala B-7 or similar strain. The cadmium-ion tolerance of the strain B-7 was determined as $2,700{\mu}g/ml$ of cadmium-ion by density gradient agar plate method. The strain B-7 grew well in an aqueous medium containing $1,000{\mu}g/ml$ of cadmium-ion.

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Regeneration of Yeast Protoplast in Hansenula anomala var. anomala and Saccharomyces cerevisiae (Hansenula anomala var. anomala와 Saccharomyces cerevisiae의 원형질체 재생에 관한 연구)

  • 구영조;박완수;신동화;유태종
    • Microbiology and Biotechnology Letters
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    • v.13 no.2
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    • pp.145-149
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    • 1985
  • Studies were conducted on the conditions for yeast protoplast regeneration in Hansenula anomala var.anomala FRI YO-32 and Saccharomyces cerevisiae. Protoplasts lysed when suspended in hypotonic solutions of KCI, and the least degree of osmolysis was shown in the hypertonic solution containing 1.4M KCI for the strain FRI YO-32 or 0.8M KCI for S. cerevisiae. It was considered that the concentration of agrar and KCI, and protoplast plating method were the main factors influencing regeneration of yeast protoplasts. Yeast protoplasts were regenerated very favorably when embedded in the complete protoplast regeneration media containing 3% agar as well as 0.4M KCI for the strain FRI YO-32 or 1.0M KCI for S. cerevisiae. It was shown from the relationship between protoplast formation and regeneration that the higher extent of protoplast formation, the lower extent of protoplast regeneration.

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Purification and characteristics of cadmium-binding protein from hansenula anomala (Hansenula anomala이 생성하는 cadmium-binding protein의 정제 및 특성)

  • 유대식;구본경
    • Korean Journal of Microbiology
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    • v.28 no.3
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    • pp.258-263
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    • 1990
  • A cadmium-binding protein was purified the cell-free extract of extreme cadmium tolerant Hansenula anomala B-7. The molecular weight was determined to be approximately 33, 000 and was composed two kinds of subunits having a molecular weight of 18, 000 and 14, 000, respectively. The extinction coefficient of the cadmium-binding protein was calculated to be 19.58. The amount of cadmium in the cadmium-binding protein was $9.26{\mu}{\textrm{g}}$ per $100{\mu}{\textrm{g}}$ of protein. A total of 14 amino acids were detected in the cadmium-binding protein, including aspartic acid, glycine and alanine that were present in a high quantity, but proline, valine and methionine were not found. The purified cadmium-binding protein contained a high quantity of cysteine and cadmium, and therefore this protein showed clearly the characteristics of metallothionein.

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Effect of Cadmium on Protein Synthesis of Cadmium-Ion Tolerant Hansenula anomala B-7 (카드뮴 내성 Hansenula anomala B-7의 단백질 합성에 미치는 카드뮴의 영향)

  • 유대식;송형익
    • Microbiology and Biotechnology Letters
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    • v.18 no.3
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    • pp.239-243
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    • 1990
  • In this study the authors investigated the distribution of cadmium accumulated in cadmium-iun tolerant Hansenula anomala B-7 cells and also the effect of cadmium on protein synthesis. 84.9% of the cadmium accumulated was distributed in the soluble fraction (cytosol, etc.). The intracellular protein content was decreased by cadmium (1,000 $\mu g$/ml), but the content of soluble protein preeipitated by ammonium sulfate (30-75% saturation) was increased compared with the content of it obtained from the cells grown without cadmium. Furthermore, in the cells grown with 1,000 $\mu g$/ml of cadmium t h higher molecular weight soluble protein was increased compared with the cells grown without caa, mium, but the lower molecular weight soluble protein was decreased. These results suggested that the protein synthesis was inhibited by cadmium, but synthesis of higher molecular weight soluble protein was remarkably stimulated by cadmium.

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Mechanism of Cadmium Accumulation into the Cell of Cadmium-Ion Tolerant Yeast (카드뮴 내성 효모의 세포내 카드뮴 축적 기작)

  • 유대식;송형익;정기택
    • Microbiology and Biotechnology Letters
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    • v.18 no.3
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    • pp.233-238
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    • 1990
  • The mechanism of intracellular accumulation of cadmium in a cadmium-ion tolerant yeast, Hansenula ammala B-7, which is an extreme cadmium tolerant strain and has the ability to take up a large amount of cadmium was investigated. The amounts of cadmium taken up by the scalded yeast cells were 2 to 3 times more than the value of the living cells. The living Hansenula anomala B-7 cells adsorbed 74% of cadmium taken up onto the other layer of the cells and 26% of it accumulated inside the cells. But the scalded cells adsorbed 98.3% of cadmium taken up and accumulated 1.7% of it inside the cells. A cadmium uptake and its accumulation were accelerated up to 162.3% and 275.4% by Triton X-100 in the living cells, respectively. Whereas in the scalded cell cadmium uptake was not affected by Triton X-100. Furthermore the cadmium uptake and its accumulation were strongly inhibited by metabolic inhibitors like 2,4-dinitrophenol, sodium azide and potassium cyanide in the living cells, but in the scalded cells cadmium uptake was not affected by metabolic inhibitors. These results suggested that the intracellular accumulation of cadmium by the cadmium-tolerant Hansenula anomala B-7 cells was apparently dependent of biological activity, and also gave evidence of the existance of energy-dependent system.

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Identification and Properties of Starch Utilizing Yeasts Isolated from Nuruk (누룩중의 전분자화성효모의 동정과 그 성질)

  • Ha, Duk-Mo;Kim, Dong-Chan;Hong, Suk-Min;Lee, Chul-Woo
    • Applied Biological Chemistry
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    • v.32 no.4
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    • pp.408-415
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    • 1989
  • Twenty-seven strains of starch utilizing yeasts were isolated from 30 samples of ‘Nuruk’, a traditional starter in Korea. These strains were identified as ten species belonging to four genera; Hansenula anomaly (six strains), Hansenula sydowiorum (two strains), Saccharomycopsis fibuligera (four strains), Schwanniomyces occidentalis (two strains), Candida fabianii(two strains), Candida famata(one strain), Candida hydrocarbofumarica (three strains), Candida silvicola (one strain), Candida steatolytica (four strains) and Candida tropicalis (two strains). Saccharomycopsis fibuligera Nu-01, Nu-08, Nu-12 and Nu-27 produced much amylase, and one of these, Saccharomycopsis fibuligera Nu-12 showed the highest amylase activity (16.9 IU/ml). Among the isolates, the strains of Hansenula anomala were exhibited relatively high specific growth rate in the medium used starch as a carbon source, and ethanol fermentation by the strains of Candida hydrocarbofumarica was not observed.

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