云南红豆杉细胞的悬浮培养

在云南红豆杉细胞悬浮培养中,适宜的培养基为B5,接种量为0．5～0．8g干重细胞／100ml培养基,2,4－D浓度为1．0mg／L;培养细胞的生长周期约30d;培养基中较高浓度的蔗糖（40g／L）可提高紫杉醇含量;添加的椰子汁（CM）、酪蛋白氨基酸（C）和水解乳蛋白（LH）3种有机添加剂均能提高培养细胞中紫杉醇的含量,但只有CM和CA能促进细胞的生长。于B5培养基中添加不同浓度的NH4NO3对培养细胞无明显影响。     

光照和培养基对内生真菌棘豆链格孢Alternaria oxytropis苦马豆素含量的影响

以小花棘豆内生真菌棘豆链格孢Alternaria oxytropis野生株OW7.8及其酵母氨酸还原酶基因缺失突变株M1为材料,研究它们在不同培养基上和不同光照下菌落生长速率与苦马豆素含量。结果表明：OW7.8在胡萝卜葡萄糖琼脂培养基上暗培养时生长速度最快,为(2.57±0.17)mm/d,而M1则在马铃薯葡萄糖琼脂培养基上暗培养时生长速度最快,为(4.93±0.10mm)/d。不同培养基和光照条件下,相同菌株苦马豆素的含量差异不显著（P>0.05）;不同菌株在相同培养条件下其苦马豆素含量差异显著（P<0.05）。     

培养基及培养条件对冬虫夏草菌固体发酵产分生孢子的影响

为获得冬虫夏草菌固体发酵产分生孢子的最优工艺,以野生分离的冬虫夏草菌为材料,对其固体发酵产分生孢子的培养基及培养条件进行了研究。试验结果表明：泥炭土为最佳基础培养基,该培养基中冬虫夏草菌气生菌丝生长一般,但产分生孢子最多,可达4.2×10³个/g;泥炭土培养基中添加0.1‰ IAA（吲哚乙酸）、0.1‰ IBA（吲哚丁酸）和0.1‰ NAA（萘乙酸）能促进冬虫夏草菌气生菌丝的生长和分生孢子的产生,其分生孢子达8.1×10³个/g;该基础培养基中,冬虫夏草菌于18℃培养30d后,在10℃、相对湿度45%、蓝光照射进行诱导,分生孢子可达1.0×10⁴个/g。本研究建立了一种大量获取冬虫夏草菌分生孢子的方法,为冬虫夏草繁育奠定了基础。     

两种纯培养外生菌根真菌对柴油的降解效率

采用紫外法和GC-MS,研究了柴油污染情况下（10 g·L^-1）外生菌根真菌铆钉菇和双色蜡蘑的生长特点及对柴油的降解效率.结果表明：铆钉菇和双色蜡蘑均能利用柴油作为唯一碳源生长.经过14 d培养,在柴油含量为10 g·L^-1液体培养基内,铆钉菇和双色蜡蘑的质量降解率分别为31.32%和39.90%,且主要减少的是16～21碳烃.不同培养基对外生菌根真菌的降解能力也有显著影响.虽然外生菌根真菌在含有葡萄糖的培养基上的生物量是对照（未添加葡萄糖）的2～5 倍,但其对柴油的降解能力明显受到抑制.高浓度的无机氮对外生菌根真菌的降解效率有一定的提高作用,但效果不明显.     

根结线虫天敌真菌及其高效菌株筛选

本文报道捕食和寄生南方根结线虫(Meloidogyne incognita)和爪哇根结线虫(M.javanica)的天敌真菌6属14种。其中Arthrobotrys candida A.cladodes var.macroides,A.musiformis,Monacrosporium cionopagum,M.doedycoides,Drechmeria coniospora,Harposporium crassum,H.lilliputanum,Myzocytium humicola和Verticillum coccospora为我国新纪录种。室内测定结果表明:GACA 1B(Arthrobotrys oligospora)、GACM 102(Monacrosporium doedycoides)菌株对南方根结线虫和爪哇根结线虫均具极高的捕食率,接种线虫7天后,捕食率达98%以上,接种20天后,捕食率均达100%。     

在哈尔滨地区使用液体菌种栽培红平菇技术初探

从福建三明真菌研究所(福建省三明市375000)购入红平菇优良菌株,在哈尔滨地区对其进行了用液体菌种代替固体原料的栽培技术研究。包括一级种培养基的筛选、液体菌种培养基的筛选、栽培种制作与培养以及出菇管理技术。结果表明:对于一级种,红平菇在PDA和马铃薯半组合培养基上都生长良好,菌丝洁白、粗壮、浓密,7～8d长满斜面;红平菇在玉米粉葡萄糖蛋白胨和麦麸葡萄糖蛋白胨液体培养基上生长较好,7d时菌丝长满培养液,菌丝量较多;用与平菇相似的常规方法制作栽培种、养菌处理与出菇管理,红平菇的产量达100%～150%。由于采用了液体菌种的栽培模式,从制种到采收的整个过程共需要50～60d,比二级种为固体菌种的常规方法缩短26～31d,大大地缩短了生产周期,提高了经济效益。     

根结线虫天敌真菌及其高效菌株筛选*

本文报道捕食和寄生南方根结线虫(Meloidogyne incognita)和爪哇根结线虫(M. javanica)的天敌真菌6属14种。其中 Arthrobotrys candida A．Cladodes var. macroides．A. musiformis,Monacrosporium cionopagum,M．Doedycoides Drechmeria coniospora,Hdrposporium crassum. H. lilliputanum,Myzocytlum huraicola 和 Verticillum coccospora为我国新纪录种。室内测定结果表明：GACA IB (Arthrobotrys oligospora)、GACM 102 (Monacrosporium doedycoides)菌株对南方根结线虫和爪哇根结线虫均具极高的捕食率,接种线虫7天后,捕食率达98％以上,接种20天后,捕食率均达100％。     

南方根结线虫内寄生真菌中国一新记录属

根结线虫(Meloidogyne spp.)是许多重要作物上危害严重又难防治的线虫之一。掘氏梅里属(Drechmeria)中的圆锥掘氏梅里霉(Drechmeria coniospora)在瑞士已用于根结线虫的生物防治,并被许多研究者用作研究真菌与线虫识别机制的好材料(Jansson et al., 1983)。我国以前未发现此属真菌。1990年作者从贵阳土壤里通过改良Drechsler法(张克勤等,1991)诱集到圆锥掘氏梅里霉,是我     

食真菌线虫与真菌的相互作用及其对土壤氮素矿化的影响

采用悉生培养微缩体系,探讨了食真菌线虫(燕麦真滑刃线虫)与两种真菌(真菌Ⅰ：外皮毛霉和真菌Ⅱ：丛梗孢科的一种)间的相互作用及其对土壤氮素矿化的影响．结果表明,燕麦真滑刃线虫在取食两种真菌时表现为在真菌Ⅱ上的生长优于真菌Ⅰ,两个处理的线虫数达到显著差异．食真菌线虫对真菌的取食活动促进了真菌的增殖：接种真菌Ⅱ加线虫处理中真菌Ⅱ的数量是仅接种真菌Ⅱ处理的2．5～3．5倍,增幅在整个培养期基本稳定;而接种真菌Ⅰ加线虫处理中真菌Ⅰ的数量在培养前期(10d)是仅接种真菌Ⅰ处理的1．1～2．0倍。之后增幅达5．0～5．7倍．线虫和真菌的生长及增殖基本保持同步．食真菌线虫与真菌的相互作用显著提高了土壤铵态氮和矿质态氮含量,促进了土壤氮的矿化,其中线虫与真菌Ⅰ的相互作用对提高矿质态氮含量的贡献显著大于线虫与真菌Ⅱ的相互作用。     

不同培养基对格氏线虫产量和毒力的影响

本文比较了五种人工培养基对昆虫病原格氏线虫Steinernema glaseri生长、繁殖、产量、带菌率和毒力的影响.经筛选以D培养基(鸡杂71%、猪油16%、海绵碎8%、水5%)最好,每瓶70克产量达10—26×10⁶条.其培养的格氏线虫子代带菌率最高,毒力最强.以培养基、接菌量和接线虫量这三个影响线虫产量的主要因素的正交试验表明:本组合中,接菌量的多少是影响线虫产量的主导因素.     

The physiology and ecology of a novel, obligate mycophagous flagellate

Abstract To determine if conidia of the nematophagous fungus Drechmeria coniospora are subject to predation by soil protozoa, several sandy soils were enriched with 10⁹ conidia of this fungus per g dry soil. After incubation of the samples at 20°C for three weeks, a flagellate was detected as the most dominant mycophagous protozoan. Conidia of several fungi, with minimum diameters between 2 and 16 μm, supported growth of this flagellate, irrespective of pigmentation. Bacteria however could not be used for growth, although bacteria and also latex beads of the same size were ingested. This is, to our knowledge, the first report of an obligate mycophagous soil-borne flagellate. The flagellate was able to grow at the expense of the conidia of D. coniospora in liquid culture, with a specific growth rate of about 0.1 h⁻¹; the optimum temperature was 20–24°C. Approximately 10 D. coniospora conidia were required for one flagellate division. In sterilized soil, enriched with 10⁸ D. coniospora conidia per g dry soil, the specific growth rate was 0.014 h⁻¹, when the soil was at 50 or 65% of its water-holding capacity (WHC). In drier soil, i.e. 25% WHC, no growth took place. During growth of the flagellate in soil, the number of D. coniospora was reduced by about 20%, which was in the same order of magnitude as expected on the basis of the requirement of 10 D. coniospora conidia for one flagellate division. Since many conidia remained in the soil after growth of the flagellate, we concluded that although the flagellate is an interesting organism, it does not play a very important role in the survival of D. coniospora conidia in the soil.     

Isolation and characterization of tyrosinase produced by marine actinobacteria and its application in the removal of phenol from aqueous environment

The present study was focused on screening and characterization of tyrosinase enzyme produced by marine actinobacteria and its application in phenolic compounds removal from aqueous solution. A total of 20 strains were isolated from marine sediment sample and screened for tyrosinase production by using skimmed milk agar medium. Among 20 isolates, two isolates LK-4 and LK-20 showed zone of hydrolysis and these were taken for secondary screening by using tyrosiue agar medium. Based on the result of secondary screening LK-4 was selected for further analysis, such as tyrosinase assay, protein content and specific activity of the enzyme. The tyrosinase enzyme was produced in a SS medium and was partially purified by ammonium sulfate precipitation, dialysis and SDS PAGE. The isolate （LK-4） was identified as Streptomyces espinosus using 16S rRNA gene sequencing and named as ＂Streptomyces espinosus strain LK4 （KF806735）＂. The tyrosinase enzyme was immobilized in sodium alginate which was applied to remove phenolic compounds from water. The enzyme efficiently removed the phenolic compounds from aqueous solution within few hours which indicated that tyrosinasc enzyme produced by Streptomyces espinosus strain LK-4 can be potently used for the removal of phenol and phenolic compounds from wastewater in industries.     

细茎石斛拟原球茎生长与有效成分积累的关系

目的 :研究细茎石斛拟原球茎生长规律及其与两种有效成分总生物碱和可溶性多糖积累的关系。方法 :采用液体静止培养方法培养细茎石斛拟原球茎 ,在一个周期 ( 60天 )内 ,每隔 1 0天取样 ,测定拟原球茎的鲜、干重 ,总生物碱含量和可溶性多糖含量。结果 :液体培养的细茎石斛拟原球茎生长曲线大致呈“S”型 ,拟原球茎经过 1 0d左右的延迟期后进入对数生长期 ,第 5 0d左右达到生长高峰 ,此后 ,生长缓慢 ,进入静止期。拟原球茎中总生物碱和可溶性多糖含量随着拟原球茎的生长逐渐积累 ,在培养的第 40d左右达到高峰 ,之后含量有所下降 ,这两种有效成分的积累与生长基本同步 ,且拟原球茎中两种有效成分的含量接近或超过野生植株茎中的含量。结论 :液体培养的细茎石斛拟原球茎生长曲线大致呈“S”型 ,总生物碱和可溶性多糖的积累与生长基本同步 ,且拟原球茎中两种有效成分的含量接近或超过野生植株茎中的含量     

Establishment and characterization of a human squamous cell carcinoma cell line LK-52 which produce direct activator of coagulant factor X]

Uterus origin squamous cell carcinoma cell line LK-52 was established from surgical specimen of lung metastatic nodule. LK-52 produce poorly differentiated squamous carcinoma in nude mouse, and doubling time in vitro was 38 hours. Chromosome analysis show various abnormality and main mode number was 67 and 68. LK-52 shed active procoagulant substance into culture medium. The culture medium of LK-52 shortening recalcification time of normal human plasma and factor VII or factor IX deficient plasma but not factor X deficient plasma. Procoagulant activity of LK-52 product may induced with direct activation of coagulant factor X. Procoagulant activity which produced by cancer cell may play a important roll in the unbalanced haemostasis of cancer patient.     

Effects of High K+ and Alkaline pH on Ultrastructure of Dunaliella salina Chloroplasts

It was reported that the growth of Dunaliella salina Teod. cultured in medium containing 1 mol/L NaC1 was almost completely inhibited by the addition of 100 mmol/L KC1. The high K+ (100 mmol/L KC1) treatment also significantly inhibited the photosynthetic rate of D. salina and decreased chlorophyll contents in algae. This study focuses on possible effects of high K+ or alkaline pH on the ultrastructural change of chloroplasts in D. salina. After D. salina was cultured in a medium containing 100 n,anol/L KC1 or in a medium with alkaline pH for 8 to 10 days, dramatic ultrastructural changes occurred in the chloroplasts including thylakoid swelling, volume increase of chloroplast, and significant accumulation of starch grains in chloroplasts. The results are consistent with our previous report indicating that the ultrastmctuml changes in chloroplast under high K + or alkaline pH may lead to an inhibitory effects on photosynthesis and overall growth of D. salina.     

高浓度钾抑制杜氏盐藻生长的生理机制

在含１ｍｏｌ／ＬＮａＣｌ的杜氏盐藻（Ｄｕｎａｌｉｅｌａｓａｌｉｎａ（Ｄｕｎａｌ）Ｔｅｏｄ．）培养液中加入５０ｍｍｏｌ／Ｌ以上的ＫＣｌ可观察到Ｋ＋对杜氏盐藻生长有明显的抑制作用,而当ＫＣｌ达１００ｍｍｏｌ／Ｌ时,杜氏盐藻的生长被完全抑制。另一方面,当培养液中缺乏Ｋ＋时,杜氏盐藻的生长也被显著抑制。在正常培养条件下,伴随着杜氏盐藻的生长,培养液的ｐＨ由８左右升高至１０左右,而高浓度Ｋ＋则显著抑制杜氏盐藻培养液ｐＨ的升高;而在培养液ｐＨ为７．０至１０．０的范围内,不同ｐＨ对杜氏盐藻的生长无明显影响。将杜氏盐藻在高浓度Ｋ＋条件下预处理１２ｈ以上,杜氏盐藻的光合放氧速率显著下降,光合速率下降的程度与Ｋ＋浓度的高低和预处理的时间长短呈正相关。高浓度Ｋ＋处理也引起杜氏盐藻叶绿素含量的显著下降。对经高浓度Ｋ＋预处理的杜氏盐藻的光合放氧速率与培养液中ｐＨ变化同时进行测定的结果表明,Ｋ＋抑制杜氏盐藻光合速率的同时也显著抑制了光照条件引起的培养液ｐＨ的上升。实验结果表明,Ｋ＋抑制杜氏盐藻光合作用以及抑制杜氏盐藻生长与Ｋ＋影响跨盐藻质膜的质子运输之间可能存在一定关系。     

Osteochondrosis in pigs diagnosed with computed tomography: heritabilities and genetic correlations to weight gain in specific age intervals

The aim of this study was to develop a method for scoring osteochondrosis (OC) by using information from computed tomography (CT), as well as to estimate the heritability for OC scored by means of CT (OCwCT) of the medial and lateral condyles at the distal end of the humerus or the femur of the right and left leg and the sum of these scores (OCT). In addition, we were aiming at revealing the genetic relationship between OCwCT traits and growth in different periods (days from birth to 30 kg (D30), days from 30 to 50 kg (D30_50), days from 50 to 70 kg (D50_70), days from 70 to 90 kg (D70_90), days from 90 to 100 kg (D90_100) and days from birth to 100 kg (D100)). The OCwCT was assessed for 1449 boars, and growth data were collected for these 1449 boars and additional 3779 boars tested in the same time period. All boars were tested as part of the Norsvin Landrace boar test and in the same test station. Heritabilities for OCwCT on anatomical locations varied from 0.21 (s.e. = 0.08) on the medial condyle of the right humerus to 0.06 (s.e. = 0.06) on the lateral condyle of the left femur, whereas OCT exhibited the highest heritability (h² = 0.31, s.e. = 0.09). Genetic correlations between OCT and OCwCT for the anatomical locations ranged from 0.94 (s.e. = 0.07) for OCT and OCwCT score for the medial condyle of the humerus right side to 0.26 (s.e. = 0.39) for OCT and the lateral condyle of the femur left side. Genetic correlations between D30 and OCT were medium high and unfavourable (r_g = −0.74). As the boar gain weight, the relationship between growth rate – expressed as number of days spent growing from one interval to the next – and OCT decreased to 0.12 (s.e. = 0.19, i.e. not significantly different from zero) for the trait D90_100 kg. These changes of genetic correlation coefficients coincide with the maturing of the joint cartilage and skeletal structures. In this study, we demonstrate that CT could be used for selection against OC in breeding programmes in pigs and that the genetic correlations between growth periods and OC are decreasing over time.     

Cell cycle progression delay in conditioned medium does not play a role in the repair of X-ray damage in Chinese hamster V79 cells

We tested our hypothesis that the lower survival of X-irradiated cells in growth medium (GM) relative to that in conditioned medium (CM) is due to differences in nutrient concentration levels rather than to differential effects on cell progression and growth. Chinese hamster V79 cells in log and unfed plateau phase, grown in Eagle's minimal essential medium (MEM) with 15% serum (100% GM), were irradiated. Before plating, cells were incubated in situ in various concentrations of MEM with serum (GM, normal cell progression) or MEM without serum or in CM (no cell progression). Cell survival was the lowest in 100% MEM with or without serum and increased with the decrease in MEM and serum concentrations, reaching a plateau in 40% MEM or 40% growth medium (40% MEM with 6% serum), similar to that in conditioned medium. Growth kinetics was the same in 40 and 100% growth medium, but the D0 of cells in 40% growth medium was higher than that of cells in 100% GM. Similarly, the D0 of cells in 40% MEM was higher than that of cells in 100% MEM, although cell progression was absent in both media. The radiation sensitivity of cells was the same in 40% GM with progression and in 40% MEM and CM with no progression. Cells in low-nutrient media were flatter than those in 100% MEM or GM. There was a correlation between the nutrient concentration in the medium postirradiation and the D0. This correlation was independent of the presence or absence of serum and thus independent of cell cycle progression. The cell morphology which is dependent on the nutrient concentration appears to influence the ability of a fraction of cells to repair their radiation damage.     

Growth studies on Mycobacterium BCG: establishment of growth curves and measurement of the oxygen tension of the growth medium

Mycobacterium BCG grew exponentially in shallow, static volumes of culture medium for approximately 10 days; the oxygen tension of the medium at all stages of growth was 100% saturation. Higher yields were obtained from Dubos than from glycerol-free medium. In static cultures, the oxygen tension of the culture and consequently the growth rate of BCG was dependent on the depth of the medium; active growth ceased at an oxygen tension of less than 40% saturation. BCG grew actively in a cell sediment, while cells growing in suspension made a negligible contribution to the yield.     

Expression and characterization of earthworm Eisenia foetida lumbrokinase-3 in Pichia pastoris

Lumbrokinase-3 (LK-3, AY438622), first cloned from the earthworm Eisenia foetida in our laboratory, is a component of earthworm fibrinolytic enzymes. In this study, cDNA encoding the LK-3 gene was sub-cloned into yeast pPIC9K expression vector and transformed into the Pichia pastoris GS115 cells by electroporation. High level expression of LK-3 in yeast cells was confirmed with a different induction time. The activity of expressed LK-3 was observed in fibrin plates. In addition, the expressed LK-3 protein could dissolve fibrinogen and bovine serum albumin. The use of this system for the high level production of biological protein is implicated from this study.