Difference in system of current photosynthesized carbon distribution to carbon and nitrogen compounds between rice and soybean

¹⁴CO₂ was assimilated during 10 min in leaf of rice and soybean under 21 kPa O2 (21% O₂ treatment) and 2 kPa O₂ (2% O₂ treatment) at the vegetative growth stage and flowering stage. The ¹⁴C distribution ratio to respired CO₂ and crude chemical components (sugars, polysaccharides, amino acids, organic acids, and proteins) was determined. In this paper, since emphasis was placed on the ¹⁴C distribution mechanism to carbon compounds and nitrogen compounds, the terms carbon metabolism pool (C-pool) composed of sugars and polysaccharides, and nitrogen metabolism pool (N-pool) composed of organic acids, amino acids and proteins were used. The results obtained were as follows.

¹⁴C distribution ratio to N-pool at 0 min after ¹⁴C assimilation was higher in soybean than in rice regardless of the treatments and stages, and that at 30 min after ¹⁴C assimilation under light condition markedly decreased both in rice and soybean. Therefore, especially in soybean, a large amount of photosynthesized ¹⁴C was once distributed to the N-pool, then ¹⁴C compounds in the N-pool were reconstructed into the C-pool. During this reconstruction process, ¹⁴C compounds in the N-pool were actively respired.

¹⁴C distribution to N-pool at 0 min after ¹⁴C assimilation changed slightly or did not change by the N treatment. ¹⁴C distribution to N-pool in the - N treatment of soybean (13–29 mg N g^-1 content in leaves) was higher than that in the + N treatment of rice (31–48 mg N g^-1 content in leaves). Photosynthesized carbon distribution to N-pool in rice decreased with growth, while it remained constant in soybean. Accordingly, in soybean, photosynthesized carbon was predominantly distributed to the N-pool through photorespiration and/or Calvin cycle (supplying triose-P), which was less affected by nitrogen nutrient and aging. Thus, the mechanism of photosynthesized carbon distribution to carbon and nitrogen compounds was basically regulated by inherited characters of each plant more than by the nitrogen status of leaves.

By the 2% O₂ treatment, ¹⁴C distribution to N-pool decreased in both crops regardless of N treatment, indicating that photorespiration plays an important role in the supply of the preliminarily photosynthesized carbon compounds to N-pool. In the 2% O₂ treatment, ¹⁴C distribution to N-pool was higher in soybean than in rice, indicating that triose-P transported from chloroplast was preferentially distributed to N-pool in the case of soybean.     

Identification of long needle crystals and distribution of oxalate salts in Narcissus cv. ‘Garden Giant’

Long needle crystals abundantly present in the bulb scales and the shoot sap of Narcissus cv. ‘Garden Giant’ were identified as Ca-oxalate by ¹³C-nuclear magnetic resonance and capillary electrophoresis. The Ca-oxalate crystals were distributed in every part of the plant, including tunics, shoot, flowers, basalplate, and roots. A large proportion of water-soluble oxalate was present in the roots, but not in the scales and shoot. Oxalate accumulation occurred mainly in the young new scales originating from the basal part of shoot. Most of all the oxalate in the inner new scales and the outer old scales was in the form of Ca-oxalate. The fact that Ca and oxalate contents in old scales remained constant after planting to the flowering stage indicated that Ca and oxalate in bulb scales are not reserve nutrients supporting plant growth. Alternatively Ca-oxalate accumulated in scales appeared to be a stable end-product.     

Localization of MT2a Gene promoter expression is different from the site(s) of copper accumulation in the roots of transgenic Arabidopsis thaliana

Accumulation of mRNA for MT2a, a metallothionein of Arabidopsis thaliana, is known to be upregulated by excess copper (Cu). We compared the localization of the promoter activity of the MT2a gene and the accumulation site(s) of CU in the roots of transgenic A. thaliana. Open reading frame of the β-glucuronidase (GUS) gene was fused with the MT2a gene promoter and introduced into A. thaliana. Strong GUS activity was observed in the region near or within the stele in the presence of CU at a high concentration (high-CU condition). Electron probe X-ray micro-analysis demonstrated that under high-CU conditions, CU accumulated most abundantly in the cortex, where GUS activity was not significantly induced. These results indicate that the sites showing the MT2a promoter activity and CU accumulation did not coincide with each other, suggesting that CU is not a direct activator of the MT2a promoter.     

Effect of placement of coated urea fertilizer on root growth and rubidium uptake activity in soybean plant

Abstract

We reported in the previous paper (Takahashi et al. 1991) that the deep placement of slow release N fertilizer (coated urea) contributed to a stable increase of soybean (Glycine max L. Merr.) yield. In the previous study we observed that the deep placement of coated urea did not depress appreciably the nitrogen fixation by root nodules although fertilizer N was efficiently utilized. We assumed that the N absorbed from the roots in the deep layers did not cause nodule senescence, contributed to the maintenance of the leaf activity during the maturation stage, and that the increase in the availability of carbohydrate and N improved seed production. In the current report the effects of placement of coated urea fertilizer on the root growth and activity were studied by measuring the root dry weight and Rb absorption activity.     

Rapid and reversible nitrate inhibition of nodule growth and N2 fixation activity in soybean (Glycine max (L.) Merr.)

Nodulated soybean (Glycine max. (L) Merr. cv. Williams) plants were hydroponically cultured, and various combinations of 1-week culture with 5 or 0 mm nitrate were applied using 13-d-old soybean seedlings during three successive weeks. The treatments were designated as 0-0-0, 5-5-5, 5-5-0, 5-0-0, 5-0-5, 0-5-5, and 0-0-5, where the three sequential numbers denote the nitrate concentration (mm) applied in the first-second-third weeks. The size of the individual nodule was measured periodically using a slide caliper. All the plants were harvested after measurement of the acetylene reduction activity (ARA) at the end of the treatments. In the 0-0-0 treatment, the nodules grew continuously during the treatment period. Individual nodule growth was immediately suppressed after 5 mm nitrate supply. However, the nodule growth rapidly recovered by changing the 5 mm nitrate solution to a 0 mm nitrate solution in the 5-0-0 and 5-5-0 treatments. In the 5-0-5 treatment, nodule growth was completely inhibited in the first and the third weeks with 5 mm nitrate, but the nodule growth was enhanced in the second week with 0 mm nitrate. The nodule growth response to 5 mm nitrate was similar between small and large size nodules. After the 5-5-5, 5-0-5, 0-0-5, and 0-5-5 treatments, where the plants were cultured with 5 mm nitrate in the last third week, the ARA per plant was significantly lower compared with the 0-0-0 treatment. On the other hand, the ARA after the 5-0-0 and 5-5-0 treatments was relatively higher than that after the 0-0-0 treatment, possibly due to the higher photosynthate supply associated with the vigorous vegetative growth of the plants supplemented with nitrate nitrogen. It is concluded that both soybean nodule growth and N₂ fixation activity sensitively responded to the external nitrate level, and that these parameters were reversibly regulated by the current status of nitrate in the culture solution, possibly through sensing of the nitrate concentration in roots and / or nodules.     

Photoassimilate partitioning in hypernodulation mutant of soybean (Glycine max (L.) Merr.) NOD1-3 and its parent williams in relation to nitrate inhibition of nodule growth

Nodule growth of a hypernodulating soybean (Glycine max (L.) Merr.) mutant line NOD1-3 was compared to that of its wild-type parent cv. Williams from 14 to 18 days after planting (DAP) in the absence of nitrate treatment (hereafter referred to as “0 mM treatment”) or with 5 mM nitrate treatment. The growth rate determined by increase in the diameter of the nodules was relatively lower in the mutant NOD1-3 than that of the parent Williams under nitrogen-free conditions (0 mM nitrate). The inhibition of nodule growth by 5 mM nitrate started at 1 d after the onset of the nitrate treatment in Williams, while the inhibition did not occur before the application of the nitrate treatment for 2 d in NOD1-3. The nodule growth was completely inhibited after 2 d in Williams and after 3 d in NOD1-3 during the 5 mM nitrate treatment period. After 4 d of 5 mM nitrate treatment, the nodule dry weight decreased by 22% in NOD1-3 and by 58% in Williams, respectively. The treatment with 5 mM nitrate decreased the acetylene reduction activity (ARA) in NOD1-3 by 60% per plant and by 50% per nodule g DW and these parameters were less sensitive to the treatment than those in Williams in which the inhibition rate was 90% per plant and 80% per nodule g DW. These results indicate that NOD1-3 is partially nitrate-tolerant in terms of individual nodule growth as well as total nodule dry weight and Nz fixation activity. A whole shoot of Williams and NOD1-3 plants was exposed to ¹⁴CO₂ for 120 min followed by 0 or 5 mM nitrate treatment for 2 d, and the partitioning of the photoassimilates among the organs was analyzed. Under 0 mM nitrate treatment, the percentages of the distribution of ¹⁴C radioactivity between the nodules and roots were 63 and 37% in Williams and 89 and 11% in NOD1-3. Under the 5 mM nitrate conditions, the percentages of the distribution of ¹⁴C between the nodules and roots changed to 14 and 86% in Williams and 39 and 61% in NOD1-3, respectively. These results indicated that the hypernodulating mutant NOD1-3 supplied a larger amount of photoassimilates to the nodules than to the roots under nitrogen-free conditions, and that the nitrate depression of photoassimilate transport to the nodules was less sensitive than that of the parent line.     

Mobilization of the active transposon mPing in interspecific hybrid rice between Oryza sativa and O. glaberrima

Miniature Ping (mPing) is the first active miniature inverted-repeat transposable element to be identified in rice, and its mobilization is activated by stress treatments. We have examined the mobilization of mPing in four NERICA (New Rice for Africa) lines and 13 interspecific lines. All 17 lines are inbred progenies derived from crosses between Oryza sativa variety WAB56-104 as the recurrent parent and the O. glaberrima variety CG14 as the donor parent. We found that 16 of the 17 lines studied inherited mPing together with its autonomous partner, Pong, from WAB56-104. Transposon display of mPing disclosed polymorphic banding patterns among these lines. Most importantly, seven of the lines displayed clear polymorphic banding patterns for mPing, indicating that mPing might have been mobilized in these lines. Locus-specific PCR analysis also confirmed the mobilization of mPing. These results signify that interspecific hybridization may activate the transposition of mPing. Based on these results, we discuss the potential use of the mPing system as an efficient tool for gene tagging in interspecific hybrid rice.     

Possible Role of ZPAC,Zygote-specific Proteasome Assembly Chaperone,During Spermatogenesis in the Mouse

In the mammalian testis, the ubiquitin-proteasome system plays important roles in the process that promotes the formation of mature sperm. We recently identified zygote-specific proteasome assembly phaperone (ZPAC), which is specifically expressed in the mouse gonads and zygote. ZPAC mediates a unique proteasome assembly pathway in the zygote, but the expression profile and function of ZPAC in the testis is not fully understood. In this study, we investigated the possible role of ZPAC during mouse spermatogenesis. First, we analyzed the expression of ZPAC and 20S proteasome subunit α4/PSMA7 in the adult mouse testis. ZPAC and α4 were expressed in spermatogonia, spermatocytes, and round spermatids. In elongating spermatids, ZPAC was expressed until step 10, whereas expression of α4 persisted until step 12. We then examined the expression profile of ZPAC and α4 in a mouse model of experimental unilateral cryptorchidism. Consistent with appearance of morphologically impaired germ cells following cryptorchidism, the ZPAC protein level was significantly decreased at 4 days post induction of experimental cryptorchidism (D4) compared with the intact testis, although the amount of α4 protein persisted at least until D10. Moreover, intense ZPAC staining was co-localized with staining of annexin V, an early indicator of apoptosis in mammalian cells, in germ cells of cryptorchid testis, but ZPAC was also expressed in germ cells showing no detectable expression of annexin V. These results suggest that ZPAC plays a role during spermatogenesis and raises the possibility that 20S proteasome mediated by ZPAC may be involved in the regulation of germ cell survival during spermatogenesis.