Gupta S, Agrawal S C
Department of Botany, University of Allahabad, Allahabad, India.
Folia Microbiol (Praha). 2004;49(5):549-56. doi: 10.1007/BF02931532.
Urea at 200 ppm (probably serving as a nitrogen source), liquid Bold's basal medium at pH 7.5, temperature of about 22 degrees C and light intensity of about 40 micromol m(-2) s(-1) for 16 h a day induced rapid and/or abundant zoospores formation and zoosporangia dehiscence and favored zoospore liberation, speed and motility time period in the green alga Rhizoclonium hieroglyphicum. However, factors such as water stress (2 and 4 % agarized media, liquid media with 0.2-0.4 mol/L NaCl, 5-60 min blot-dryness of filaments), pH extremes of liquid media (at < or =6.5 and > or =9.5), temperature shock in liquid media (5 and 35 degrees C for > or =5 min), UV exposure (0.96-3.84 kJ/m2), lack of all nutrients from liquid medium (double distilled water), darkness, and presence of "heavy" metals (1-25 ppm Cu, Fe, Zn, Hg, Ni, Co) or organic substances (200-600 ppm captan or DDT, 800 and 1000 ppm 2,4-D, 50 and 400 ppm indole-3-acetic acid (3-IAA), 1000 and 2000 ppm urea, 100 and 200 ppm thiourea) in liquid media decreased and/or delayed at various levels either zoosporangia survival, zoospore formation or zoosporangia dehiscence and/or the rate of zoospore liberation from zoosporangia, zoospore speed and time period of motility in the media or totally inhibited all these processes. 3-IAA at 50 and 400 ppm induced zoosporangial papilla to grow into a tube-like projection of about 30-120 microm in length. Zoosporangial dehiscence rather than zoospore formation or zoosporangia survival, and zoospore motility period rather than zoospore speed are probably more sensitive to various adverse environmental factors. The rate of zoospores liberation from zoosporangium (possibly related directly to some extent on the zoospore number inside) is probably independent of zoospore speed in the medium.
200 ppm的尿素(可能作为氮源)、pH值为7.5的液体Bold基础培养基、约22摄氏度的温度和约40微摩尔·米-2·秒-1的光照强度,每天光照16小时,可诱导绿藻象形根枝藻快速和/或大量形成游动孢子以及游动孢子囊开裂,并有利于游动孢子的释放、速度和游动时间。然而,诸如水分胁迫(2%和4%的琼脂化培养基、含0.2 - 0.4摩尔/升氯化钠的液体培养基、藻丝5 - 60分钟的吸干干燥)、液体培养基的极端pH值(小于或等于6.5和大于或等于9.5)、液体培养基中的温度冲击(5和35摄氏度,持续大于或等于5分钟)、紫外线照射(0.96 - 3.84千焦/平方米)、液体培养基中所有营养物质的缺乏(双蒸水)、黑暗以及液体培养基中“重金属”(1 - 25 ppm的铜、铁、锌、汞、镍、钴)或有机物质(200 - 600 ppm的克菌丹或滴滴涕、800和1000 ppm的2,4 - 二氯苯氧乙酸、50和400 ppm的吲哚 - 3 - 乙酸(IAA)、1000和2000 ppm的尿素、100和200 ppm的硫脲)的存在,会在不同程度上降低和/或延迟游动孢子囊的存活、游动孢子的形成或游动孢子囊的开裂,和/或游动孢子从游动孢子囊中释放的速率、游动孢子的速度以及在培养基中的游动时间,或者完全抑制所有这些过程。50和400 ppm的IAA可诱导游动孢子囊的乳头状突起生长成约30 - 120微米长的管状突起。游动孢子囊的开裂而非游动孢子的形成或游动孢子囊的存活,以及游动孢子的游动时间而非游动孢子的速度,可能对各种不利环境因素更为敏感。游动孢子从游动孢子囊中释放的速率(可能在一定程度上直接与内部的游动孢子数量有关)可能与培养基中游动孢子的速度无关。