首页 > 最新文献

Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects最新文献

英文 中文
Electric birefringence of actin 肌动蛋白的电双折射
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90096-8
Syoyu Kobayashi, Hiroshi Asai, Fumio Oosawa

The polymerization of actin was followed by the measurement of electric birefringence. Small elementary polymers of actin which appeared at very low salt concentrations or at the initial stage of polymerization showed a positive electric birefringence. They were oriented with the long axis parallel to the electric field. This was mainly due to a permanent dipole moment in the direction of the long axis, the magnitude of which was estimated from the Kerr constant to be about 75 Debye units per actin monomer. The elementary polymers grew into normal F-actin which showed a large negative electric birefringence. That is, F-actin filaments were oriented in the direction perpendicular to the field. Therefore, the electric structure of F-actin filaments was completely different from that of elementary small polymers. The negative electric birefringence of F-actin was cancelled by the addition of H-meromyosin.

在肌动蛋白聚合后进行电双折射测量。在极低盐浓度或聚合初始阶段出现的肌动蛋白小的基本聚合物表现出正的电双折射。它们以平行于电场的长轴定向。这主要是由于长轴方向上的永久偶极矩,其大小由克尔常数估计为每个肌动蛋白单体约75德拜单位。基本聚合物生长成正常的f -肌动蛋白,表现出较大的负电双折射。也就是说,f -肌动蛋白丝在垂直于场的方向上定向。因此,f -肌动蛋白丝的电结构与基本小聚合物完全不同。F-actin的负电双折射被H-meromyosin的加入所抵消。
{"title":"Electric birefringence of actin","authors":"Syoyu Kobayashi,&nbsp;Hiroshi Asai,&nbsp;Fumio Oosawa","doi":"10.1016/0926-6577(64)90096-8","DOIUrl":"10.1016/0926-6577(64)90096-8","url":null,"abstract":"<div><p>The polymerization of actin was followed by the measurement of electric birefringence. Small elementary polymers of actin which appeared at very low salt concentrations or at the initial stage of polymerization showed a positive electric birefringence. They were oriented with the long axis parallel to the electric field. This was mainly due to a permanent dipole moment in the direction of the long axis, the magnitude of which was estimated from the Kerr constant to be about 75 Debye units per actin monomer. The elementary polymers grew into normal F-actin which showed a large negative electric birefringence. That is, F-actin filaments were oriented in the direction perpendicular to the field. Therefore, the electric structure of F-actin filaments was completely different from that of elementary small polymers. The negative electric birefringence of F-actin was cancelled by the addition of H-meromyosin.</p></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90096-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23802383","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: 61
Observations on the fluorescence emitted by slices of rat liver and avian salt gland 大鼠肝脏和鸟盐腺切片荧光观察
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90094-4
G.D.V. Van Rossum

The fluorescence emitted by slices of rat liver and sea-gull salt gland which were irradiated with light at 366 mμ, showed a peak at 468 mμ under aerobic conditions. The intensity of the fluorescence decreased during the early stages of incubation of 38°, due largely to the effects of the ultraviolet exciting radiation. Under aeobic conditions of incubation the fluorescence intensity fell by 40–60, and the remained relatively constant for a period of several hours; in anaerobic conditions the fall in intensity continued to lower levels. During the period in which the fluorescence of aerobic slices constant, quantitatively reproducible increases in tissue fluorescence were caused by the onset of tempory anoxia, by the addition of succinate to the medium and by the treatments which stimulated ion transport in the slices.

在366 μ m光照射下,大鼠肝脏和海鸥盐腺切片的荧光在468 μ m处出现峰值。在38°孵育的早期阶段,荧光强度下降,主要是由于紫外线激发辐射的影响。在好氧条件下,荧光强度下降40-60,并在数小时内保持相对恒定;在无氧条件下,下降强度继续降低。在好氧切片的荧光保持不变期间,定量可重复的组织荧光增加是由暂时性缺氧的开始、在培养基中添加琥珀酸盐和刺激切片中离子运输的处理引起的。
{"title":"Observations on the fluorescence emitted by slices of rat liver and avian salt gland","authors":"G.D.V. Van Rossum","doi":"10.1016/0926-6577(64)90094-4","DOIUrl":"10.1016/0926-6577(64)90094-4","url":null,"abstract":"<div><p>The fluorescence emitted by slices of rat liver and sea-gull salt gland which were irradiated with light at 366 mμ, showed a peak at 468 mμ under aerobic conditions. The intensity of the fluorescence decreased during the early stages of incubation of 38°, due largely to the effects of the ultraviolet exciting radiation. Under aeobic conditions of incubation the fluorescence intensity fell by 40–60, and the remained relatively constant for a period of several hours; in anaerobic conditions the fall in intensity continued to lower levels. During the period in which the fluorescence of aerobic slices constant, quantitatively reproducible increases in tissue fluorescence were caused by the onset of tempory anoxia, by the addition of succinate to the medium and by the treatments which stimulated ion transport in the slices.</p></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90094-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72908467","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: 11
Studies on ion transport 离子输运研究
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90107-X
G.P. Brierley, E. Murer, R.L. O'Brien
{"title":"Studies on ion transport","authors":"G.P. Brierley,&nbsp;E. Murer,&nbsp;R.L. O'Brien","doi":"10.1016/0926-6577(64)90107-X","DOIUrl":"10.1016/0926-6577(64)90107-X","url":null,"abstract":"","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90107-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87197672","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: 17
Potassium transport in Neurospora 钾在神经孢子虫中的转运
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90101-9
Carolyn W. Slayman , E.L. Tatum

  • 1.

    1. Wild-type Neurospora crassa, growing logarithmically in minimal medium, contains 180 ± 16 mM intracellular K+ and 14 ± 2 mM Na+. It requires K+ but not Na+ for growth. Over a wide range of extracellular K+ concentrations (0.3 to 100 mM), the cells maintain a constant, high level of intracellular K+ (180 mM) and rapid growth occurs. Below 0.3 mM, the internal K+ concentration falls and growth is inhibited.

  • 2.

    2. When cells are harvested from logarithmic growth and resuspended in distilled water or in 1 mM sodium azide, they show no significant loss of internal K+ for at least 1 h. Exposure to the polyene antibiotic nystatin (30 μg/ml) or the decapeptide antibiotic tyrocidine (20 μg/ml) causes most of the internal K+ to be lost within 2 min. Both antibiotics are thought to attack the plasma membrane of sensitive organisms.

  • 3.

    3. Neurospora exchanges its intracellular K+ quite rapidly for extracellular K+ or Rb+, but only slowly for Na+.

  • 4.

    4. These experiments were undertaken to provide a backgroun for microelectrode studies with Neurospora and for the isolation of a K+-transport mutant.

1.1. 野生型粗神经孢子菌在最小培养基中呈对数生长,细胞内K+含量为180±16 mM, Na+含量为14±2 mM。它需要K+而不需要Na+来生长。在细胞外K+浓度的大范围内(0.3至100 mM),细胞保持恒定的高水平细胞内K+ (180 mM),并发生快速生长。在0.3 mM以下,内部K+浓度下降,生长受到抑制。当细胞从对数生长中收获并在蒸汽水或1mm叠氮化钠中重悬时,它们在至少1小时内没有显示出内部K+的显著损失。暴露于多烯抗生素制霉菌素(30 μg/ml)或十肽抗生素酪胺(20 μg/ml)会导致大部分内部K+在2分钟内损失。这两种抗生素被认为会攻击敏感生物体的质膜。神经孢子菌胞内K+与胞外K+或Rb+的交换速度较快,而Na+的交换速度较慢。这些实验是为神经孢子菌的微电极研究和K+转运突变体的分离提供了背景。
{"title":"Potassium transport in Neurospora","authors":"Carolyn W. Slayman ,&nbsp;E.L. Tatum","doi":"10.1016/0926-6577(64)90101-9","DOIUrl":"10.1016/0926-6577(64)90101-9","url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. Wild-type <em>Neurospora crassa</em>, growing logarithmically in minimal medium, contains 180 ± 16 mM intracellular K<sup>+</sup> and 14 ± 2 mM <em>Na</em><sup>+</sup>. It requires K<sup>+</sup> but not Na<sup>+</sup> for growth. Over a wide range of extracellular K<sup>+</sup> concentrations (0.3 to 100 mM), the cells maintain a constant, high level of intracellular K<sup>+</sup> (180 mM) and rapid growth occurs. Below 0.3 mM, the internal K<sup>+</sup> concentration falls and growth is inhibited.</p></span></li><li><span>2.</span><span><p>2. When cells are harvested from logarithmic growth and resuspended in distilled water or in 1 mM sodium azide, they show no significant loss of internal K<sup>+</sup> for at least 1 h. Exposure to the polyene antibiotic nystatin (30 μg/ml) or the decapeptide antibiotic tyrocidine (20 μg/ml) causes most of the internal K<sup>+</sup> to be lost within 2 min. Both antibiotics are thought to attack the plasma membrane of sensitive organisms.</p></span></li><li><span>3.</span><span><p>3. Neurospora exchanges its intracellular K<sup>+</sup> quite rapidly for extracellular K<sup>+</sup> or Rb<sup>+</sup>, but only slowly for Na<sup>+</sup>.</p></span></li><li><span>4.</span><span><p>4. These experiments were undertaken to provide a backgroun for microelectrode studies with Neurospora and for the isolation of a K<sup>+</sup>-transport mutant.</p></span></li></ul></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90101-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81540387","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: 135
The inhibition of transport of glucose into human erythrocytes by 2,3,4,6-tetra[O-acethyl]-β-d-glucopyranose 2,3,4,6-四[o -乙基]-β-d-葡萄糖吡喃糖对葡萄糖转运到人红细胞的抑制作用
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90099-3
L. Lacko, M. Burger

2,3,4,6-tetra[O-acetyl]-β-d-glucopyranose penetrated into human erythrocytes following a transport mechanism different from that of glucose. However, TAG interacted with the glucose-carrier ssytem, inhibiting the transport of glucose to a variable extent, depending on experimental conditions.

Comparison of the inhibitory effect of TAG on exchange and non-exchange transport showed that it affected a suppression of glucose transport similar to that obtained by lowering the temperature.

The presence of subtances in the matrix of the membrane which regulate the movement of carriers, interacting similarly to TAG, is tentatively suggested.

2,3,4,6-四[o -乙酰基]-β-d-葡萄糖通过不同于葡萄糖的转运机制进入人红细胞。然而,TAG与葡萄糖载体系统相互作用,根据实验条件不同,在不同程度上抑制葡萄糖的运输。比较TAG对交换转运和非交换转运的抑制作用表明,TAG对葡萄糖转运的抑制作用类似于降低温度所获得的抑制作用。初步认为,膜基质中存在与TAG类似的调节载体运动的物质。
{"title":"The inhibition of transport of glucose into human erythrocytes by 2,3,4,6-tetra[O-acethyl]-β-d-glucopyranose","authors":"L. Lacko,&nbsp;M. Burger","doi":"10.1016/0926-6577(64)90099-3","DOIUrl":"10.1016/0926-6577(64)90099-3","url":null,"abstract":"<div><p><span><math><mtext>2,3,4,6-</mtext><mtext>tetra</mtext><mtext>[O-</mtext><mtext>acetyl</mtext><mtext>]-β-</mtext><mtext>d</mtext><mtext>-</mtext><mtext>glucopyranose</mtext></math></span> penetrated into human erythrocytes following a transport mechanism different from that of glucose. However, TAG interacted with the glucose-carrier ssytem, inhibiting the transport of glucose to a variable extent, depending on experimental conditions.</p><p>Comparison of the inhibitory effect of TAG on exchange and non-exchange transport showed that it affected a suppression of glucose transport similar to that obtained by lowering the temperature.</p><p>The presence of subtances in the matrix of the membrane which regulate the movement of carriers, interacting similarly to TAG, is tentatively suggested.</p></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90099-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23802386","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
Optical absorption of the porphyrin free radical formed in a reversible photochemical reaction 光吸收卟啉自由基形成的可逆光化学反应
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90112-3
D. Mauzerall , G. Feher
{"title":"Optical absorption of the porphyrin free radical formed in a reversible photochemical reaction","authors":"D. Mauzerall ,&nbsp;G. Feher","doi":"10.1016/0926-6577(64)90112-3","DOIUrl":"10.1016/0926-6577(64)90112-3","url":null,"abstract":"","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90112-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23802397","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: 20
Transport of neutral, dibasic and N-methyl-substituted amino acids by rat intestine 中性、二碱性和n -甲基取代氨基酸在大鼠肠内的转运
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90100-7
P. Reed Larsen, Joan E. Ross, Donald F. Tapley

The ability of everted sacs of rat small intestine to transport neutral, dibasic and N-methyl-substituted amino acids has been determined. The data obtained support the suggestion that three separate amino acid-transport systems are present in rat intestine.

测定了大鼠小肠外翻囊转运中性、双碱性和n -甲基取代氨基酸的能力。获得的数据支持了大鼠肠道中存在三个独立的氨基酸运输系统的建议。
{"title":"Transport of neutral, dibasic and N-methyl-substituted amino acids by rat intestine","authors":"P. Reed Larsen,&nbsp;Joan E. Ross,&nbsp;Donald F. Tapley","doi":"10.1016/0926-6577(64)90100-7","DOIUrl":"10.1016/0926-6577(64)90100-7","url":null,"abstract":"<div><p>The ability of everted sacs of rat small intestine to transport neutral, dibasic and <em>N</em>-methyl-substituted amino acids has been determined. The data obtained support the suggestion that three separate amino acid-transport systems are present in rat intestine.</p></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90100-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23802387","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: 84
The macromolecular parameters of ascites tumor cell H-RNA 腹水肿瘤细胞H-RNA的大分子参数
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90105-6
S.N. Timasheff

A concerted analysis of sedimentation, light scattering and small-angle X-ray-scattering data on high-molecular-weight Ehrlich ascites tumor cell RNA has been carried out. The three sets of data have been found to be in quantitative agreement with a compact structure consisting of short double-helical roldlike subunits, which account for 90% of the RNA mass.

对高分子量埃利希腹水肿瘤细胞RNA的沉降、光散射和小角度x射线散射数据进行了协调分析。这三组数据已被发现在定量上与一个紧凑的结构组成的短双螺旋棒状亚基一致,占RNA质量的90%。
{"title":"The macromolecular parameters of ascites tumor cell H-RNA","authors":"S.N. Timasheff","doi":"10.1016/0926-6577(64)90105-6","DOIUrl":"10.1016/0926-6577(64)90105-6","url":null,"abstract":"<div><p>A concerted analysis of sedimentation, light scattering and small-angle X-ray-scattering data on high-molecular-weight Ehrlich ascites tumor cell RNA has been carried out. The three sets of data have been found to be in quantitative agreement with a compact structure consisting of short double-helical roldlike subunits, which account for 90% of the RNA mass.</p></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90105-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23803754","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: 3
Biochimica et biophysica acta, vol. 88 (1964) 生物化学与生物物理学报》,第 88 卷(1964 年)
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90117-2
{"title":"Biochimica et biophysica acta, vol. 88 (1964)","authors":"","doi":"10.1016/0926-6577(64)90117-2","DOIUrl":"https://doi.org/10.1016/0926-6577(64)90117-2","url":null,"abstract":"","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90117-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136455413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photodimerization of urocanic acid in vitro and in vivo 尿尿酸在体外和体内的光二聚化
Pub Date : 1964-11-29 DOI: 10.1016/0926-6577(64)90092-0
J.H. Anglin Jr., Mark Allen Everett

  • 1.

    1. Irradition of urocanic acid or urocanate frozen in aqueous solution with 280–320-mμ light produced a photodimer which was isolated by gradient elution from an anion-exchange resin.

  • 2.

    2. A similar substance was shown to be present in dilute acid extracts of guinea-pig epidermis after irradiation with 280–320-mμ light.

  • 3.

    3. The photodimer formed with 280–320-mμ light when irradiated in solution with 254-mμ light was converted to urocanic acid and smaller amounts of several other products.

  • 4.

    4. Irradiation of crystalline urocanic acid or its solutions does not produce an accumulation of the photodimer.

1.1. 用280 - 320 μ m的光照射冷冻在水溶液中的尿毒酸或尿毒酸盐,产生光二聚体,通过梯度洗脱从阴离子交换树脂中分离得到。在280 ~ 320 μ m的光照射下,豚鼠表皮的稀酸提取物中也存在类似的物质。280 ~ 320 μ m光形成的光二聚体在254 μ m光的照射下转化为尿尿酸和少量其他几种产物。照射结晶尿酸或其溶液不会产生光二聚体的积累。
{"title":"Photodimerization of urocanic acid in vitro and in vivo","authors":"J.H. Anglin Jr.,&nbsp;Mark Allen Everett","doi":"10.1016/0926-6577(64)90092-0","DOIUrl":"10.1016/0926-6577(64)90092-0","url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. Irradition of urocanic acid or urocanate frozen in aqueous solution with 280–320-mμ light produced a photodimer which was isolated by gradient elution from an anion-exchange resin.</p></span></li><li><span>2.</span><span><p>2. A similar substance was shown to be present in dilute acid extracts of guinea-pig epidermis after irradiation with 280–320-mμ light.</p></span></li><li><span>3.</span><span><p>3. The photodimer formed with 280–320-mμ light when irradiated in solution with 254-mμ light was converted to urocanic acid and smaller amounts of several other products.</p></span></li><li><span>4.</span><span><p>4. Irradiation of crystalline urocanic acid or its solutions does not produce an accumulation of the photodimer.</p></span></li></ul></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"1964-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90092-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"23802379","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: 11
期刊
Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1