• 한국환경과학회지
• /
• 제7권6호
• /
• pp.853-857
• /
• 1998

Purification of the isocitrate lyase extracted from Microbacterium laevaniformans was investigated. The isocitrate lyase was purified 43.6 folds by the following continuous treatment with ammonium sulfate fraction, DEAE-cellulose, DEAE-sephacel and Sephadex G-200 chromatography. The purified isocitrate lyase was showed to be a single protein band by polyacrylamide gel electrophoresis. The molecular weight of the purified isocitrate lyase was estimated 54,000 Da by the SDS-polyacrylamide gel electrophoresis. The Km and Vmax values for isocitrate were estimated to be 0.83mM and 0.33units/ml, respectively. Activity of isocitrate lyase was inhibited by cystein-HCl and glutathione.

• 한국미생물·생명공학회지
• /
• 제15권6호
• /
• pp.420-424
• /
• 1987

Saccharomycopsis lipolytica ATCC 44601 과 MX9-11RX8 온도감수성 변이균주의 isocitrate lyase는 조추출액을 ammonium sulfate 분획, Toyo Peal HW-55F gel filtration, DEAE-Cellulose ion exchange chromatography 등의 방법에 의하여 각각 54배, 87배 분리 정제되었다. 정제효소의 subunit 분자량은 59,000이고 Sephadex G-200 gel filtration에 의한 native enzyme 은 230,000이므로 이 효모의 isocitrate lyase는 같거나 비슷한 subunit 4개로 구성된 tetramer이며, 최적 pH는 6.9이었다.

• 미생물학회지
• /
• 제31권3호
• /
• pp.230-236
• /
• 1993

Micrococcus luteus 가 생산하는 isocitrate lyase 의 효소단백질을 ammonium sulfate precipitation, DEAE-cellulose, DEAE-sephacel, 1차 Sephadex G-200, 2 차 Sephadex G-200 column chromatography 과정을 통하여 분리 정제하였으며 정제된 효소의 분자량과 효소학적 특성을 조사하였다. 정제된 isocitrate lyase 는 상기 정제 과정을 통하여 10.2%의 회수율과 38.8 의 정제도를 나타내었으며, 전기영동시 단일밴드를 얻을 수 있었고, SDS-PAGE 에 의해 측정된 분자량을 약 60,000이며 1개의 subunit 로 나타났다. 본 효소의 최적 pH 는 7.5이었으며, 최적 온도는 $40^{\circ}C$ 부근이었고 $45^{\circ}C$까지는 안정하였다. 2가 금속염의 첨가시$ Mg^{2+}$ 를 제외한 다른 금속이온들은 효소활성을 저해하는 것으로 나타났으며 $Mg^{2+}$의 농도는 5 mM 에서 최대활성을 나타내었다. 또한 기질인 DL-isocitrate 의 $K_{m}$ 치는 0.95 mM 로 나타났으며, thiol 화합물의 첨가시 cysteine 은 1mM, glutathione과 $\beta$-mercaptoethanol 은 5 mM 의 농도에서 효소활성이 최대에 달하였다.

• 한국식품영양학회지
• /
• 제1권1호
• /
• pp.25-32
• /
• 1988

Properties of purified isocitrate lyase from Saccharomycopsis lipolytica ATCC 44601 and MX9-11RX8 temperature-sensitive mutant were investigated. Purified isocitrate lyase from temperature-sensitive mutant was indistinguishable from the wild type enzyme with respect to the isoelectric pH(5.3), the thermostability and Km value for threo-Ds-Isocitrate(about 0.2 mM). When isocitrate lyase induced by acetate minimal medium at 33$^{\circ}C$, MX9-11RX8 mutant did not express enzyme activity but did synthesize polypeptide chain whose electrophoretic mobilities were equal to those of the purified enzymes.

• 미생물학회지
• /
• 제24권2호
• /
• pp.194-197
• /
• 1986

Malonate kinase and isocitrate lyase were induced in Acinetobacter calcoaceticus grown on malonate as a sole carbon source but repressed by succinate. The induction of those two enzymes was stimulated by dibutyryl cyclic adenosine 3', 5'-monophosphate, indicating that the expression of their genes for those enzymes is dependent on cyclic adenosine 3', 5'-monophosphate.

• 한국미생물·생명공학회지
• /
• 제15권6호
• /
• pp.414-419
• /
• 1987

Saccharomycopsis lipolytica의 isocitrate lyase에 대한 온도감수성 변이의 특성과 이 효소의 생화학적성질을 조사하기 위한 기초연구로서 isocitrate lyase 결손변이 균주인 MX9-11(Icl-)로부터 온도감수성을 나타내는 복귀 변이균주를 3균주 분리하고 그중 활성의 회복이 가장 높은 MX9-11RX8 균주의 성질을 조사하였다. MX9-11RX8 복귀 변이균주는 탄소원으로서 초산을 사용하였을 때 온도의 증가에 따라서 isocitrate lyase의 생성량과 비생성 속도가 감소하여 33$^{\circ}C$에서는 거의 효소를 합성하지 않았으며, 온도를 23$^{\circ}C$에서 33$^{\circ}C$로 올렸을 때 효소의 합성은 바로 정지하였지만 균체증식은 계속되었다. 한편 n-hexadecane을 탄소원으로 사용하였을 때에도 온도감수성을 나타내었으며, 온도의 shift up 후에도 isocitric acid 생산은 거의 변화가 없었다.

• 한국식품영양과학회지
• /
• 제17권3호
• /
• pp.277-281
• /
• 1988

Saccharomycopsis lipolytica의 citrate와 isocitrate의 생산에 미치는 itaconate의 영향을 조사하였다. Itaconate는 isocitrate lyase의 활성을 저해하며 저해율은 0.8mM 농도에서 약 80% 이었고, 개열반응에서는 직선적인 불경쟁적 저해를 나타내었으며 저해상수 Ki값은 0.18mM이었다. Itaconate는 glucose 배지에서는 균의 생육에 영향을 미치지 않았지만 n-hexadecane 배지에서는 균의 생육을 심하게 저해하였다. 한편 itaconate의 첨가량을 증가시킴에 따라 총산에 대한 isocitrate의 생산 비율은 n-hexadecane배지에서는 약 80%까지 증가하였으나 glucose배지에서는 거의 변화가 없었다.

• Journal of Microbiology and Biotechnology
• /
• 제15권3호
• /
• pp.652-655
• /
• 2005

This paper describes the development of an enzymatic assay system for the identification of inhibitors of isocitrate lyase (ICL), one of the key enzymes of the glyoxylate cycle that is considered as a new target for antifungal drugs. A 1.6 kb DNA fragment encoding the isocitrate lyase from Candida albicans ATCC10231 was amplified by PCR, cloned into a vector providing His-Patch-thioredoxin-tag at the N-terminus, expressed in Escherichia coli, and purified by metal chelate affinity chromatography. The molecular mass of the purified ICL was approximately 62 kDa, as determined by SDS-PAGE, and the enzyme activity was directly proportional to incubation time and enzyme concentration. The effects of itaconate-related compounds on ICL activity were also investigated. Among them, itaconic acid, 3-nitropropionate, and oxalate had strong inhibitory activities with $IC_{50}$ values of 5.8, 5.4 and $8.6\;{mu}g/ml$, respectively. These inhibitors also exhibited antifungal activity on YPD agar media containing acetate as a sole carbon source, albeit at high concentration. The results indicate that the C. albicans ICL may be a regulatory enzyme playing a crucial role in fungal growth and is a prime target for antifungal agents.

• Applied Biological Chemistry
• /
• 제31권2호
• /
• pp.137-142
• /
• 1988

Saccharomycopsis lipolytica ATCC 44601에서 정제한 isocitrate lyase 반응산물의 축합반응과 개열반응은 $30^{\circ}C$, pH 7.0에서 분석되었다. Glyoxylate와 succinate의 축합반응에서 Km값은 각각 0.06 mM과 0.21 mM이었고, 개열 반응에서 glyoxylate는 직선적인 경쟁적 저해를, succinate는 직선적인 비경쟁적 저해를 나타내었으며 이때 Ki 값은 각각 0.22 mM과 0.82 mM이었다. 그러므로 이 kinetic분석은 이 효소가 축합 반응에서 glyoxylate가 succinate보다 먼저 결합하는 정서반응기구인 것을 나타내었다. 3-Bromopyruvate(BrP)의 불활성화는 포화 kinetics를 나타내면서 효소를 불가역적으로 불활성화하였으며 반감기는 0.15분이고 $K_{BrP}$는 0.032 mM이었으며, 기질과 반응생성물들을 불활성화에 대하여 보호작용이 있었다.

• Journal of Microbiology and Biotechnology
• /
• 제16권7호
• /
• pp.1158-1162
• /
• 2006

The glyoxylate cycle can conserve carbons and adequately supply tricarboxylic acid (TCA) cycle intermediates for biosynthesis when microorganisms grow on $C_{2}$ carbon sources. It has been reported that isocitrate lyase (ICL1), a key enzyme of the glyoxylate cycle, is highly induced when Magnaporthe grisea, the causal agent of rice blast, infects its host. Therefore, the glyoxylate cycle is considered as a new target for antifungal agents. A 1.6-kb DNA fragment encoding the ICL1 from M. grisea KJ201 was amplified by PCR, cloned into a vector providing His-tag at the N-terminus, expressed in Escherichia coli, and purified using Ni-NTA affinity chromatography. The molecular mass of the purified ICL1 was approximately 60 kDa, as determined by SDS-PAGE. The ICL1 inhibitory effects of TCA cycle intermediates and their analogs were investigated. Among them, 3-nitropropionate was found to be the strongest inhibitor with an $IC_{50}$ value of $11.0{\mu}g/ml$. 3-Nitropropionate inhibited the appressorium development in M. grisea at the ${\mu}M$ level, whereas conidia germination remained unaffected. This compound also inhibited the mycelial growth of the fungus on minimal medium containing acetate as a $C_{2}$ carbon source. These results suggest that ICL1 plays a crucial role in appressorium formation of M. grisea and is a new target for the control of phytopathogenic fungal infection.