一株产共轭亚油酸乳酸菌的鉴定及其特性

从酸菜汁中分离筛选到一株产共轭亚油酸(CLA)能力较高的乳酸菌。经鉴定,确定为植物乳杆菌Lactobacliius plantarum。微氧条件可提高CLA的产量,催化亚油酸(LA)生成CLA的酶受着LA的诱导。37℃对细胞生长和CLA生成最为有利。对数生长期为6～12h,18h后进入稳定期。在14～22h,CLA生成量快速增加,24h时达到最高值。该菌的培养物经萃取、甲酯化后,进行了气相色谱分离,生成的CLA产物为c9/t9,c11-CLA和t10,c12-CLA异构体的混合物。     

共轭亚油酸对前脂肪细胞增殖分化的影响

培养前脂肪细胞3T3-L1,MTT法检测CLA对3T3-L1增殖的影响;以油红O染色检测3T3-L1分化过程胞内脂肪的堆积;同时采用逆转录-聚合酶链式反应(RT-PCR)检测CLA对过氧化物酶体增殖物激活受体γ2(PPARγ2)mRNA表达的影响.结果显示: t10,c12-CLA以及CLA混合物对前脂肪细胞3T3-L1增殖均有显著的抑制作用(P<0.05).油红染色比色结果表明,t10,c12-CLA具有显著的抑制脂肪分化作用(P<0.05).RT-PCR结果显示,在前脂肪细胞3T3-L1分化过程中,经100 μmol/L t10,c12-CLA和50 μmol/L t10,c12-CLA处理后PPARγ2 mRNA表达量分别为对照组的52.1%,83.0%.     

植物乳杆菌ZS2058在磷酸盐缓冲液体系中生物转化共轭亚油酸

植物乳杆菌ZS2058是从泡菜中筛选到一株具有转化共轭亚油酸能力的乳酸菌。该菌株在MRS培养基中经0.5mg/mL的亚油酸诱导培养后,所获得的菌体细胞具有较强的转化能力。文中就植物乳杆菌ZS2058水洗细胞在磷酸盐缓冲液体系中生物转化共轭亚油酸进行了深入研究。在非厌氧条件下,植物乳杆菌ZS2058在亚油酸浓度为1mg/mL,湿细胞质量浓度约为150mg/mL,120r/min、37℃的条件下反应24h后,能将亚油酸转化为共轭亚油酸和羟基脂肪酸,其中c9,t11-CLA占所产生的CLA总量的96.4%,产量可高达312.4μg/mL,说明该菌株有很强的专一性。随着反应进一步进行,反应至36h时,c9,t11-CLA含量逐渐减少,伴随着大量羟基脂肪酸的产生;并且,以CLA(c9,t11-CLA和t10,c12-CLA的混合样品)为底物进行反应时,c9,t11-CLA被转化为羟基脂肪酸。由此可知,c9,t11-CLA可能是该菌株生物转化LA过程中的一个中间产物。     

共轭亚油酸诱导人结肠癌细胞Caco-2凋亡的作用

共轭亚油酸（conjugated linoleic acid,CLA）有着多种异构体以及多种生理活性,如抗癌、减肥、抗动脉粥样硬化等。本研究主要对c9,t11-CLA和t9,t11-CLA两种异构体的混合物诱导人结肠癌细胞Caco-2凋亡的作用及可能机制进行了探讨。采用MTT方法、透射电镜观察、流式细胞术检测和RT—PCR方法,研究了CLA混合物抑制Caco-2细胞增殖,诱导Caco-2细胞凋亡的作用及可能机制。实验结果证明,c9,t11-CLA和t9,t11-CLA混合物能抑制Caco-2细胞的增殖,并可诱导Caco-2的凋亡。随着所用的CLA混合物浓度的增加以及作用时间的延长,细胞凋亡率增加。通过RT—PCR分析,Caco-2细胞中的caspase 3的mRNA的表达随着CLA混合物浓度的增加而上调。这两种CLA的混合物可抑制Caco-2细胞的增殖,诱导Caco-2的凋亡,而caspase 3的表达上调可能与细胞凋亡密切相关。     

大麦虫不同虫态甲醇粗提物化学成分的分析和比较

为了探寻大麦虫Zophobas morio变态发育过程中化学成分的变化, 本研究利用薄层色谱技术对大麦虫的3个虫态(幼虫、 蛹和成虫)甲醇粗提物中的化学成分进行分析和比较, 利用柱色谱技术、 核磁共振氢谱技术（¹H MR）和气相色谱-质谱联用技术（GC-MS）对蛹甲醇粗提物进行重点分析。结果表明： 虫蛹甲醇粗提物中含有幼虫和成虫甲醇粗提物中不存在的化学成分。对虫蛹甲醇粗提物进行针对性的结构研究, 共鉴定出10个脂肪酸。其中, 存在于大麦虫虫蛹中的10-十六碳酮酸、 10-十八碳酮酸为首次从自然界昆虫中获得; (8E, 11E)-8, 11-十八碳烯酸、 (9Z, 12Z)-9, 12-十八碳烯酸、 (9Z, 12Z, 15Z)-9, 12, 15-十八碳烯酸、 8-(3-辛基-2-环氧乙烷基)辛酸和8-(2-辛基环丙烷基)辛酸为首次从大麦虫中发现。以上研究结果为针对大麦虫不同生物阶段的开发利用提供新的理论依据。     

绿槽枝衣的化学成分

从地衣绿槽枝衣( Sulcaria virens) 中分离得到一个新的亚油酸异丙叉衍生物, 通过波谱学方法包括2D-NMR 确定其化学结构为: 9, 10-O-异丙叉基- (12 Z)-十八碳烯酸(1) 。同时还得到其它12 个已知化合物:( 9 Z, 12 Z )-十八碳二烯酸(2), 扁枝衣二酸(3), ( R ) -松萝酸(4), 枕酸甲酯( 5), 黑茶渍素(6) , virensic acid ( 7), abieslactone (8), 3α-羟基羊毛甾-7, 24-二烯-26, 23 R-内酯(9), 蒲公英赛醇(10 ), 蒲公英赛酮 ( 11 ), (22 E , 24 R )-5α, 8α-过氧麦角甾-6, 22-二烯-3β-醇(12) 和2, 2′-四氢角鲨烯(13)。     

植物气味化合物与斜纹夜蛾性信息素的协同作用

为提高现有性信息素对雄蛾的引诱活性, 本研究通过大量的田间试验探索植物气味化合物与斜纹夜蛾Spodoptera litura性信息素（顺9, 反11-十四碳二烯乙酸酯∶顺9, 反12-十四碳二烯乙酸酯=10∶1）的协同作用机制。从斜纹夜蛾寄主植物和花的气味化合物中, 选择9种有代表性的化合物, 并以一定剂量分别加入到斜纹夜蛾性信息素诱芯中, 在田间测试对雄蛾的引诱活性。结果表明: 在测试的9种植源性化合物中, 发现一定剂量(每个诱芯加入0.4 mg)的苯乙醛(PAA), 具有显著提高斜纹夜蛾性信息素的引诱作用, 而高剂量的苯乙醛则强烈抑制性信息素的引诱活性; 此外, 其他各种浓度的测试化合物或混合物对性信息素则没有统计上显著的增效作用。不同剂量的苯乙醛单个化合物及各种植物气味化合物组成的混合物对斜纹夜蛾也有微弱的引诱作用。苯乙醛必须要与性信息素的完整组分(以10∶1比例混合的顺9, 反11-十四碳二烯乙酸酯和顺9反, 12-十四碳二烯乙酸酯)混合才能起作用, 缺少顺9, 反12-十四碳二烯乙酸酯则没有引诱活性。本研究证明, 苯乙醛作为理想的性信息素诱芯增效剂, 可应用于建立更理想的斜纹夜蛾性信息素诱杀技术, 对性诱害虫防治和测报具有应用价值。     

Assay and comparison of chemical constituents of crude methanol extracts from different developmental stages of darkling beetle Zophpbas morio ( Coleoptera: Tenebrionidae)

为了探寻大麦虫Zophobas morio变态发育过程中化学成分的变化,本研究利用薄层色谱技术对大麦虫的3个虫态(幼虫、蛹和成虫)甲醇粗提物中的化学成分进行分析和比较,利用柱色谱技术、核磁共振氢谱技术(1HNMR)和气相色谱-质谱联用技术(GC-MS)对蛹甲醇粗提物进行重点分析.结果表明:虫蛹甲醇粗提物中含有幼虫和成虫甲醇粗提物中不存在的化学成分.对虫蛹甲醇粗提物进行针对性的结构研究,共鉴定出10个脂肪酸.其中,存在于大麦虫虫蛹中的10-十六碳酮酸、10-十八碳酮酸为首次从自然界昆虫中获得;(8E,11E)-8,11-十八碳烯酸、(9Z,12Z)-9,12-十八碳烯酸、(9Z,12Z,15Z)-9,12,15-十八碳烯酸、8-(3-辛基-2-环氧乙烷基)辛酸和8-(2-辛基环丙烷基)辛酸为首次从大麦虫中发现.以上研究结果为针对大麦虫不同生物阶段的开发利用提供新的理论依据.     

共轭亚油酸对草鱼生长、肌肉成分、谷草转氨酶及谷丙转氨酶活性的影响

<正>共轭亚油酸(Conjugated linoleic acid,CLA)是十八碳二烯酸(亚油酸)的同分异构体,其共同特征为两个双键直接通过一个碳-碳单键连接,没有被亚甲基隔开。共轭亚油酸的双     

马桑种子油的脂肪酸成分

马桑(Coriaria sinica Maxim.)系马桑科植物,广布于我国山西、陕西、甘肃、河南、湖北、湖南、四川、广西、贵州和云南等省。野生资源十分丰富。其脂肪酸成分未见报道。为此,成都土产站提供种子,分别交给北京植物研究所和我所进行脂肪酸成分研究,我们两单位的结论是相同的,即主要成分为13-羟基顺-9-反-11十八碳二烯酸     

Selective production of cis-9,trans-11 isomer of conjugated linoleic acid from trans-vaccenic acid methyl ester by Delacroixia coronata

Aims:  Bio-process development for isomer selective and efficient production of cis -9, trans -11-octadecadienoic acid (CLA) from trans -vaccenic acid ( t -VA, trans -11-octadecenoic acid) through microbial fatty acid Δ9-desaturation reaction.
Methods and Results:  A total of 550 strains of fungi and yeasts were screened for CLA production from t -VA through Δ9 desaturation. Delacroixia coronata IFO 8586 was selected as a potent producer of CLA from t -VA. Efficient CLA production was observed during cultivation in medium supplemented with the methyl ester of t -VA ( t -VAME). Under the optimal conditions with 33·3 mg ml⁻¹ of t -VAME as substrate, 10·5 mg ml⁻¹ CLA was produced by D. coronata IFO 8586 after 7 days of cultivation in the medium containing dextrin (5·0%), tryptone (2·0%) and thiourea (0·83 μmol ml⁻¹). The strain produced the cis -9, trans -11 isomer of CLA selectively (98% of total CLA), with a small amount of the trans -9, trans -11 isomer (2% of total CLA), mainly in the form of triacylglycerols (69% of total CLA).
Conclusions:  A practical bio-process for selective production of cis -9, trans -11 isomer of CLA using filamentous fungus D. coronata IFO 8586 was successfully established.
Significance and Impact of the Study:  Isomer selective bio-process for the practical production of cis -9, trans -11-CLA was first established. The process is benefitable for expanding the application of CLA for medicinal and nutraceutical purposes.     

一株产共轭亚油酸瘤胃细菌Streptococcus infantarius RB111的筛选与鉴定

从内蒙古鄂尔多斯山羊瘤胃中分离筛选到1株产共轭亚油酸的瘤胃细菌RB111,该菌株的cis9,trans11-CLA和trans10,cis12-CLA总产量为269.2 mg/L,其中cis9,trans11-CLA占52.64%,trans10,cis12-CLA占47.36%。对菌株RB111进行了形态学观察、生理生化鉴定、脂肪酸组成分析以及16S rRNA基因序列分析。16S rRNA基因序列分析结果表明该菌株与婴儿链球菌(Streptococcus infantarius)的模式菌株NCDO 599的序列相似性为99%,该菌株的形态特征及生理生化特性与文献报道的Streptococcus infantarius一致。脂肪酸组成分析结果显示,菌株RB111的细胞脂肪酸主要成分是C16:0、C18:1ω9c和C18:0,3种脂肪酸占脂肪酸总量的60.64%。综合以上结果,菌株RB111被鉴定为婴儿链球菌Streptococcus infantarius。     

Conjugated linoleic acid and inflammatory cell signalling

Conjugated linoleic acids (CLA) are a family of polyunsaturated fatty acids (PUFA), some isomers occurring naturally in beef and dairy products and others being formed as a result of bihydrogenation of vegetable oils to form margarine. Synthetic and natural sources of CLA may have beneficial effects in a range of inflammatory conditions including colitis, atherosclerosis, metabolic syndrome and rheumatoid arthritis. Most of the biological effects have been attributed to the cis9, trans11- (c9, t11-) and the trans10, cis12- (t10, c12-) isomers. Evidence suggests that c9, t11-CLA is responsible for the anti-inflammatory effect attributed to CLA while t10, t12-CLA appears to be responsible for anti-adipogenic effects. This review will focus on the effects of CLA on the inflammatory components associated with insulin resistance, atherosclerosis and Th1 mediated inflammatory disease, at a cellular, systemic and clinical level. Whist CLA may ameliorate certain aspects of the inflammatory response, particularly within cellular and animal models, the relevance of this has yet to be clarified within the context of human health.     

Conjugated linoleic acid reduction of murine mammary tumor cell growth through 5-hydroxyeicosatetraenoic acid

Conjugated linoleic acid (CLA) is a dietary fatty acid that has been shown to reduce tumorigenesis and metastasis in breast, prostate and colon cancer in animals. However, the mechanism of its action has not been clarified. The goal of this study was to determine whether CLA altered mouse mammary tumor cell growth and whether specific metabolites of the lipoxygenase pathway were involved in CLA action. Both t10, c12-CLA and a lipoxygenase inhibitor, but not c9, t11-CLA or linoleic acid (LA), reduced mouse mammary tumor cell viability and growth by inducing apoptosis and reducing cell proliferation. t10, c12-CLA reduced the production of the 5-lipoxygenase metabolite, 5-hydroxyeicosatetraenoic acid (5-HETE). That effect was not seen with c9, t11-CLA or LA. Adding 5-HETE back to tumor cells reduced the t10, c12-CLA effect on both apoptosis and cell proliferation. These data suggest that t10, c12-CLA reduction of tumor cell growth may involve the suppression of the 5-lipoxygenase metabolite, 5-HETE, with subsequent effects on apoptosis and cell proliferation.     

Effects of conjugated linoleic acid isomers on monocyte, macrophage and foam cell phenotype in atherosclerosis

Conjugated linoleic acid (CLA) is a generic term denoting a group of naturally occurring isomers of linoleic acid (18:2, n6) that differ in the position or geometry (i.e. cis or trans) of their double bonds. The predominant isomers in ruminant fats are cis-9,trans-11 CLA (c9,t11-CLA), and trans-10,cis-12 CLA (t10,c12-CLA). The biological activities of CLA have received considerable attention because of its protective effects in cancer, immune function, obesity and atherosclerosis. Importantly, dietary administration of a blend of the two most abundant isomers of CLA, has been shown to inhibit the progression and induce the regression of pre-established atherosclerosis in the ApoE?/? murine model. Studies investigating the mechanisms involved in CLA induced protective effects are continually emerging with results from both in vitro and in vivo models yielding confounding and often inconsistent results depending on both the isomer of CLA and the species under investigation. The purpose of this review is to comprehensively discuss the effects of CLA on monocyte/macrophage function in atherosclerosis. This review also discusses the possible mechanisms through which CLA mediates its atheroprotective effects with a particular emphasis on the migratory capacity of the monocyte and the inflammatory and cholesterol homeostasis of the macrophage.     

t10c12-CLA maintains higher bone mineral density during aging by modulating osteoclastogenesis and bone marrow adiposity

Conjugated linoleic acid (CLA) has been shown to positively influence calcium and bone metabolism. Earlier, we showed that CLA (equal mixture of c9t11-CLA and t10c12-CLA) could protect age-associated bone loss by modulating inflammatory markers and osteoclastogenesis. Since, c9t11-CLA and t10c12-CLA isomers differentially regulate functional parameters and gene expression in different cell types, we examined the efficacy of individual CLA isomers against age-associated bone loss using 12 months old C57BL/6 female mice fed for 6 months with 10% corn oil (CO), 9.5% CO + 0.5% c9t11-CLA, 9.5% CO + 0.5% t10c12-CLA or 9.5% CO + 0.25% c9t11-CLA + 0.25% t10c12-CLA. Mice fed a t10c12-CLA diet maintained a significantly higher bone mineral density (BMD) in femoral, tibial and lumbar regions than those fed CO and c9t11-CLA diets as measured by dual-energy-X-ray absorptiometry (DXA). The increased BMD was accompanied by a decreased production of osteoclastogenic factors, that is, RANKL, TRAP5b, TNF-alpha and IL-6 in serum. Moreover, a significant reduction of high fat diet-induced bone marrow adiposity was observed in t10c12-CLA fed mice as compared to that of CO and c9t11-CLA fed mice, as measured by Oil-Red-O staining of bone marrow sections. In addition, a significant reduction of osteoclast differentiation and bone resorbing pit formation was observed in t10c12-CLA treated RAW 264.7 cell culture stimulated with RANKL as compared to that of c9t11-CLA and linoleic acid treated cultures. In conclusion, these findings suggest that t10c12-CLA is the most potent CLA isomer and it exerts its anti-osteoporotic effect by modulating osteoclastogenesis and bone marrow adiposity.     

Potent inhibitory effect of trans9, trans11 isomer of conjugated linoleic acid on the growth of human colon cancer cells

This study compared the growth inhibitory effects of pure conjugated linoleic acid (CLA) isomers [cis(c)9,c11-CLA, c9,trans(t)11-CLA, t9,t11-CLA, and t10,c12-CLA] on human colon cancer cell lines (Caco-2, HT-29 and DLD-1). When Caco-2 cells were incubated up to 72 h with 200 μM, each isomer, even in the presence of 10% fetal bovine serum (FBS), cell proliferation was inhibited by all CLA isomers in a time-dependent manner. The strongest inhibitory effect was shown by t9,t11-CLA, followed by t10,c12-CLA, c9,c11-CLA and c9,t11-CLA, respectively. The strongest effect of t9,t11-CLA was also observed in other colon cancer cell lines (HT-29 and DLD-1). The order of the inhibitory effect of CLA isomer was confirmed in the presence of 1% FBS. CLA isomers supplemented in the culture medium were readily incorporated into the cellular lipids of Caco-2 and changed their fatty acid composition. The CLA contents in cellular lipids were 26.2±2.7% for t9,t11-CLA, 35.9±0.3% for c9,t11-CLA and 46.3±0.8% for t10,c12-CLA, respectively. DNA fragmentation was clearly recognized in Caco-2 cells treated with t9,t11-CLA. This apoptotic effect of t9,t11-CLA was dose- and time-dependent. DNA fragmentation was also induced by 9c,11t-CLA and t10,c12-CLA. However, fragmentation levels with both isomers were much lower than that with t9,t11-CLA. t9t11-CLA treatment of Caco-2 cells decreased Bcl-2 levels in association with apoptosis, whereas Bax levels remained unchanged. These results suggest that decreased expression of Bcl-2 by t9t11-CLA might increase the sensitivity of cells to lipid peroxidation and to programmed cell death, apoptosis.