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Review
. 2015 Jul 17:21:2073-8.
doi: 10.12659/MSM.894758.

Mitochondria, Chloroplasts in Animal and Plant Cells: Significance of Conformational Matching

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Review

Mitochondria, Chloroplasts in Animal and Plant Cells: Significance of Conformational Matching

George B Stefano et al. Med Sci Monit. .

Abstract

Many commonalities between chloroplasts and mitochondria exist, thereby suggesting a common origin via a bacterial ancestor capable of enhanced ATP-dependent energy production functionally linked to cellular respiration and photosynthesis. Accordingly, the molecular evolution/retention of the catalytic Qo quinol oxidation site of cytochrome b complexes as the tetrapeptide PEWY sequence functionally underlies the common retention of a chemiosmotic proton gradient mechanism for ATP synthesis in cellular respiration and photosynthesis. Furthermore, the dual regulatory targeting of mitochondrial and chloroplast gene expression by mitochondrial transcription termination factor (MTERF) proteins to promote optimal energy production and oxygen consumption further advances these evolutionary contentions. As a functional consequence of enhanced oxygen utilization and production, significant levels of reactive oxygen species (ROS) may be generated within mitochondria and chloroplasts, which may effectively compromise cellular energy production following prolonged stress/inflammationary conditions. Interestingly, both types of organelles have been identified in selected animal cells, most notably specialized digestive cells lining the gut of several species of Sacoglossan sea slugs. Termed kleptoplasty or kleptoplastic endosymbiosis, functional chloroplasts from algal food sources are internalized and stored within digestive cells to provide the host with dual energy sources derived from mitochondrial and photosynthetic processes. Recently, the observation of internalized algae within embryonic tissues of the spotted salamander strongly suggest that developmental processes within a vertebrate organism may require photosynthetic endosymbiosis as an internal regulator. The dual presence of mitochondria and functional chloroplasts within specialized animal cells indicates a high degree of biochemical identity, stereoselectivity, and conformational matching that are the likely keys to their functional presence and essential endosymbiotic activities for over 2.5 billion years.

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Figures

Figure 1
Figure 1
The prokaryotic cell is characterized by a general lack of highly structured intracellular organelles but displays intracellular regions of functionality with some membrane enhancements, e.g., mesosome. We surmise that with time this relatively simple structure became more elaborate, adding membrane surface area to perform work, enhancing a major function like respiration. In all probability the stimulus was solar energy, causing the photolysis of water. This cell was driven in this direction because it provided a new coping strategy for, counter-intuitively, DNA advancement. This evolving cellular architecture could not survive on its own given the presence of by products it produced, e.g., ROS, which are basically toxic to unprotected intracellular components, notably DNA. This evolutionary self protection mechanism was further advanced when oxygen levels increased as a result of photosynthesis. In all probability the cellular oxygen toxicity issue was partly solved by having a “bacterium” develop in a “bacterium”, becoming a eukaryotic cell, which could harvest specific bond energy. This also aided in ROS protection with a more structured and protected environment for this new intracellular relationship to evolve, having a plentiful energy supply for novel DNA expression. Accordingly, a major free radical and free radical creator was effectively removed via chloroplasts, which originated in a similar manner as mitochondria. Thus, it is not surprising to find both types of “bacteria” in the same cell and others where only one is present. Furthermore, given this close evolvement, enslavement was not an issue in this circumstance because each “cell” used the same or similar chemical messengers, stabilizing what appears to be a precarious relationship. Indeed, bidirectional communication served as the process for eukaryotic cellular communication/cooperation, which allowed for metazoan evolution. Interestingly, metazoan evolution is still highly dependent on the intracellular communication with its endogenous bacterial components from which it evolved, e.g., intracellular and extracellular (gut microbiome). The vulnerability expresses itself in “mitochondrial dysfunction” in that it can be so complicated and diverse depending on the tissue region affected. We further surmise that hypoxia plays a major role in triggering mitochondrial dysfunction since this entire relationship depends on a continuously ongoing energy processing system[2,21]. Briefly, the evolutionary advancement of eukaryotic cells requires this homeostatic energy balance to maintain its multicomponent and faceted existence. Any deviation from the thermodynamically stabilized life form creates a pathology wherever it occurs. This process may also represent the deleterious mechanisms that may be associated with aging.

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