• 한국미생물·생명공학회지
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• 제9권2호
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• pp.51-57
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• 1981

토양과 sludge 에서 1,2-propanediol을 자화할 수 있는 미생물을 분리하여 이들 중 가장 많은 젖산을 생성 하는 호모 한 균주(Y-1-4)를 선정하였다. 배양액에 생성된 산은 paper chromatography와 IR spectrum에 의해서 젖산으로 확인되었다. 이 효모는 탄소원으로서 ethanol, glycerin, glucose 및 1,2-propanediol 등을 자화할 수 있었는데 1,2-propanediol 으로부터만 젖산을 생성했다. 1,2-propanediol 에서부터 젖산생성의 최적 배지 및 최적 배양조건을 검토해서 1,2-propanediol 2.0%, NH$_4$Cl 0.5%, KH$_2$PO$_4$ 0.1%, MgSO$_4$.7$H_2O$ 0.05%, FeSO$_4$.7$H_2O$ 0.025%, yeast extract 0.04%와 CaCO$_3$ 0.3%를 함유하는 배지를 3$0^{\circ}C$에서 4일간 진탕 배양한 결과 젖산 생성량은 liter당 12.1gram 이었다.

• KSBB Journal
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• 제26권5호
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• pp.439-442
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• 2011

1,2-propanediol (1,2-PD) is a commodity chemical that is currently produced from petrochemical derivatives. Saccharomyces cerevisiae is well characterized and a successful industrial microorganism to enable the improvement of the 1,2-propanediol production by metabolic engineering. A recombinant S. cerevisiae M3G3 was used to produce 1,2-propanediol. S. cerevisiae M3G3 is the diploid strain that contains 3 copies of mgs (methylglyoxal synthase) and gldA (glycerol dehydrogenase). S. cerevisiae M3G3 was cultivated at various culture conditions by changing culture temperature, glucose concentration, and inducer concentration. Also the effect of induction time was studied to optimize the production of 1,2-propanediol. Batch and fed-batch cultivation of S. cerevisiae M3G3 was performed by using a 5 L jar fermenter. The highest concentration of 1,2-propanediol in batch cultivation was 0.86 g/L and it was further improved to 1.33 g/L in fed-batch cultivation.

• 한국수정란이식학회지
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• 제8권1호
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• pp.25-30
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• 1993

소 난자의 시험관내 수정시 이성체인 1, 2 propanediol과 1, 3 propanediol과의 동결보호제의 이용에 대한 독성효과를 조사하였다. 프랑스에 있는 도축장의 난소에서 채취한 미성숙 난자 212개를 시험관내 성숙과 heparin(10$\mu$g/ml)첨가에 의한 수정 및 배양을 실시하였다. 소 난자의 시험관내 성숙과 수정시 propanediol의 독성효과를 시험한 결과 1,3 propanediol은 80%의 정상 난할분할율과 5.7%의 낮은 다핵분할구율을 나타내었다. 이것은 1,2 propanediol의 73.9%, 10.3%와 미처리대조구의 73.9%, 7.7%와 비교되었으나 처리간의 유의성은 없었다. Heparin 처리구는 1,2 propanediol의 첨가 유무에 관계없이 미처리구에 대하여 고도의 유의성 차이가 인정되었다. (P<0.05)

• Journal of Microbiology and Biotechnology
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• 제18권11호
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• pp.1797-1802
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• 2008

Saccharomyces cerevisiae was metabolically engineered to improve 1,2-propanediol production. Deletion of the tpil (triosephosphate isomerase) gene in S. cerevisiae increased the carbon flux to DHAP (dihydroxylacetone phosphate) in glycolysis, resulting in increased glycerol production. Then, the mgs and gldA genes, the products of which convert DHAP to l,2-propanediol, were introduced to the tpil-deficient strain using a multicopy plasmid. As expected, the intracellular level of methylglyoxal was increased by introduction of the mgs gene in S. cerevisiae and that of 1,2-propanediol by introduction of both the mgs and gldA genes. As a result, 1.11 g/l of 1,2-propanediol was achieved in flask culture.

• Journal of Microbiology and Biotechnology
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• 제21권8호
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• pp.846-853
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• 2011

Glycerol has become an attractive carbon source in the biotechnology industry owing to its low price and reduced state. However, glycerol is rarely used as a carbon source in Saccharomyces cerevisiae because of its low utilization rate. In this study, we used glycerol as a main carbon source in S. cerevisiae to produce 1,2-propanediol. Metabolically engineered S. cerevisiae strains with overexpression of glycerol dissimilation pathway genes, including glycerol kinase (GUT1), glycerol 3-phosphate dehydrogenase (GUT2), glycerol dehydrogenase (gdh), and a glycerol transporter gene (GUP1), showed increased glycerol utilization and growth rate. More significant improvement of glycerol utilization and growth rate was accomplished by introducing 1,2-propanediol pathway genes, mgs (methylglyoxal synthase) and gldA (glycerol dehydrogenase) from Escherichia coli. By engineering both glycerol dissimilation and 1,2-propanediol pathways, the glycerol utilization and growth rate were improved 141% and 77%, respectively, and a 2.19 g 1,2- propanediol/l titer was achieved in 1% (v/v) glycerolcontaining YEPD medium in engineered S. cerevisiae.

• Current Research on Agriculture and Life Sciences
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• 제5권
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• pp.168-172
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• 1987

광학성체인 isopropylidene glycerols로 부터 mercaptogiycerol을 합성하였다. 1,2-Isopropylideneglycerol을 tosyl화 하고 다시 tosyl group을 thiolacetate로 치환하였다. 염기성 가수분해와 산화에 의해 1,1'-dithiobis-2,3-isopropylidene-2,3-propanediol이 생성되었다. 이 화합물을 mercaptogiycerol 합성을 위해 사용함으로써 1-decenyl lithium으로 cis-S-dec-1'-enyl-2,3-isopropylidene-1-mercapto-2,3-propanediol을 생성하였다. 본 생성물은 plasmalogenase용 thioplasmaloger 기질 조제에 사용된다.

• KSBB Journal
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• 제17권3호
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• pp.255-260
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• 2002

순수 글리세롤 대신에 유지산업 부산물로써 고농도의 글리세롤이 포함된 폐액을 이용하여 1,3-PD 생산의 최적 조건을 조사하였다. 1,3-PD의 경우 혐기성 조건에서만 생성되므로 글리세롤을 1,3-PD로 전환하는 여러 미생물 중에서 절대 혐기성 균주보다 다루기 쉽고 배양하기 좋은 통성 혐기성 균주인 Klebsiella pneumcniae와 Citrobacter freundii을 비교하여 폐액의 최종 글리세롤 농도가 25 g/L일 때 1,3-PD의 수율과 균주 생육이 좋은 Klebsiella pneumoniae를 선택하였다. 1,3-PD 생산의 최적조건을 조사한 결과 폐액의 글리세롤농도를 25 g/L으로 조정하였을 때 폐액에 포함된 다른 성분의 저해를 적게 받으면서 생산수율이 가장 높았으며, 질소원으로는 corn steep powder를 1%(w/v) 첨가하였을 때 수율이 가장 높았다. 배양액을 발효조 배양에서 pH는 6.0일 때 1,3-PD 수율이 가장 높았으며 pH가 6.0이하로 낮아졌을 때 균주가 성장하지 못하고 사멸하였다. 발효 최적온도는 $35^{\circ}C$였으며 pH의 급격한 변화를 방지하기 위해 첨가한 인산염의 첨가는 효과가 없었다. 그리고 순수 글리세롤의 비교 실험에서 글리세롤 최종농도가 2.5%일 때 1,3-PD으로 수율을 보면 폐액은 53%, pure 글리세롤은 51%로 거의 비슷하였다. 글리세롤 최종 농도가 5.0%로 조정한 했을 때 1,3-PD 수율은 글리세롤함유 폐액 및 순수글리세롤의 기질농도를 2.5% 사용했을 때 보다 모두 낮아졌다. 산업적으로 비누 세제산업 부산물로 생성되는 글리세롤함유 폐액을 1,3-PD 생산에 사용하기 위해서 폐액의 글리세롤농도를 2.5% 조정했을 때 1,3-PD 수율이 순수 글리세롤을 사용했을 때와 비슷하게 생성됨을 알수 있었다. 앞으로 고농도 폐액에서 생육저해가 없이 1,3-PD을 생산할 수 있는 돌연변이 균주의 개발과 유가배양 및 연속 배양에서 최적 배양조건을 찾아야 할 것이다.

• Toxicological Research
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• 제18권1호
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• pp.1-11
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• 2002

3-Monochloro-1,2-propanediol(3-MCPD) is currently being a matter of concern because of its toxicity. 3-MCPD produced during the acid hydrolysis of soybean products has been reported to be mutagenic, neurotoxic, nephrotoxic and spermatotoxic. Howerer, the carcinogenicity of 3-MCPD is a controversial issue over the past several decades. 3-MCPD characteristically showed a variety of toxicities in reproductive system such as, decrease in sperm number and sperm motility, infertility, loss of sperm function, and weight decrease in ovary. Due to the toxicity of 3-MCPD, exposure to 3-MCPD has been proposed to be reduced to as low a level as technologically feasible. 3-MCPD can be detected in soy sauce or non-soy sauce products. The legal limit for 3-MCPD this year has been suggested to be 20 ppb（$\mu\textrm{g}$/kg）in the European Community. In Korea, the permissible level of 3-MCPD is expected to be 0.3 ppm. In this study, 3-MCPD was toxicologically evaluated in terms of risk assessment in humans.

• 한국가축번식학회지
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• 제15권2호
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• pp.133-139
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• 1991

This stduy was carried out in order to investigate the effects of concentration and equilibration time of cryoprotective agents on survival rate of slow and ultrarapidly frozen in vitro fertilized bovine embryos. In vitro fertilized bovine embryos, following dehydration by cryoprotective agents and sucrose, were slowly freezed(from 2$0^{\circ}C$ to -7$^{\circ}C$/-1$^{\circ}C$/min., from -7$^{\circ}C$ -35$^{\circ}C$/-0.2$^{\circ}C$/min. from -35$^{\circ}C$ to -38$^{\circ}C$/-0.3$^{\circ}C$/min.) by cell freezer and directly plunged into liquid nitrogen and thawed in 38$^{\circ}C$ water. Survival rate was defined by development rate to the morula and blastocyst stage after in vitro cultured and FDA test. The results are summarized as follows : 1. The survival rates of in vitro fertilized bovine embryos after slow frozen-thawing in the freezing medium of 0.25M sucrose added 2.5M glycerol, 3.0M DMSO, 2.0M propanediol and 2.5M glycerol＋2.0M propanediol were 84.3%, 85.9%, 77.8%, 74.3%, respectively. 2. The survival rates of in vitro fertilized bovine embryos after slow frozen-thawing in the freezing of 0.50M sucrose added 2.5M glycerol, 3.0M DMSO, 2.0M propanediol and 2.5M glycerol＋2.0M propanediol were 83.8%, 85.1%, 71.4%, 74.6%, respectively. 3. The survival rates of in vitro fertilized bovine embryos after ultrarapid frozen-thawing in the freezing of 0.25M sucrose added 2.5M glycerol, 3.0M DMSO, 2.0M propanediol and 2.5M glycerol＋3.0M propanediol were 69.3%, 70.8%, 63.2%, 67.1%, respectively. 4. The survival rates of in vitro fertilized bovine embryos after ultrarapid frozen-thawing in the freezing of 0.25M sucrose added 2.5M glycerol, 3.0M DMSO, 2.0M propanediol and 2.5M glycerol＋2.0M propanediol were 69.4%, 70.1%, 62.3%, 63.5%, respectively. 5. The survival rates of in vitro fertilized bovine embryos after slow and ultrarapid fromthawing in the freezing medium of sucrose added cryoprotective agents were not significant difference between 5min. and 10min. of equilibration time.

• 한국가축번식학회지
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• 제16권2호
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• pp.117-123
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• 1992

This Study was carried out ot investigate the effects of concentration and equilibration time of cryoprotective aagents on survival rate of slowly and ultrarapidly frozen porcine embryos. The porcine embryos following dehydration by cryoprotective agents and 0.25M sucrose were slowly freezed(from 2$0^{\circ}C$ to -7$^{\circ}C$/-1$^{\circ}C$/min., from -7$^{\circ}C$ to -35$^{\circ}C$/-0.2$^{\circ}C$/min., from -35$^{\circ}C$ to -38$^{\circ}C$/-0.3$^{\circ}C$/min.) by Cell Freezer and directly plunged into liquid nitrogen and thawed in 38$^{\circ}C$ water bath. Survival rate was defined as development rate to the morula and blastocyst stage after in vitro culture or by FDA test. The results are summarized as follows : 1. The survival rates of porcine embryos after slow frozen-thawing in the freezing medium of 0.25M sucrose added 2.0M glycerol, 3.0M DMSO, 2.0M propanediol or 2.0M glycerol＋2.0M propanediol was 80.6, 84.7, 75.0 or 78.8%, respectively. 2. The survival rates of porcine embryos after slow frozen-thawing in the freezing medium of 0.50M sucrose added 2.0M glycerol, 3.0M DMSO, 2.0M propanediol or 2.0M glycerol＋2.0M propanediol was 80.9, 82.4, 73.1 or 77.1%, respectively. 3. The survival rates of porcine embryos after ultrarapid frozen-thawing in the freezing medium of 0.25M sucroese added 2.0M glycerol, 3.0M DMSO, 2.0M propanediol or 2.0M glycerol＋2.0M propanediol was 65.3, 68.6, 63.2 or 59.9%, respectively. 4. The survival rates of porcine embryos after ultrapid frozen-thawing in the freezing medium of 0.50M sucrose added 2.0M glycerol, 3.0M DMSO, 2.0 propanediol or 2.0M glycerol＋2.0M propanediol was 67.5, 62.9, 56.9, or 62.8%, respectively. 5. The higher survival rate of porcine embryos was attained at the short period ofequilibration time(5min.) in the freezing medium added 0.25M sucrose and 3.0 DMSO compared to those of 10 or 20min. equilibration time in the same condition.